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Genome Sciences & Policy Certificate : All Publications (in the database)

List most recent publications in the database.    :chronological  alphabetical  combined  bibtex listing:

Royal, Charmaine D.

  1. Bulgin, D; Asnani, M; Vorderstrasse, A; Royal, C; Pan, W; Tanabe, P, Stigma and quality of life in adults with sickle cell disease in Jamaica and the United States., Psychology, health & medicine, vol. 28 no. 5 (June, 2023), pp. 1133-1147 [doi]  [abs]
  2. Wagner, JK; Yu, J-H; Fullwiley, D; Moore, C; Wilson, JF; Bamshad, MJ; Royal, CD; Genetic Ancestry Inference Roundtable Participants, , Guidelines for genetic ancestry inference created through roundtable discussions., HGG advances, vol. 4 no. 2 (April, 2023), pp. 100178 [doi]  [abs]
  3. Royal, CDM, Science, Society, and Dismantling Racism., Health equity, vol. 7 no. 1 (January, 2023), pp. 38-44 [doi]  [abs]
  4. Callier, SL; Payne, PW; Akinniyi, D; McPartland, K; Richardson, TL; Rothstein, MA; Royal, CDM, Cardiologists' Perspectives on BiDil and the Use of Race in Drug Prescribing., Journal of racial and ethnic health disparities, vol. 9 no. 6 (December, 2022), pp. 2146-2156 [doi]  [abs]
  5. Sodeke, S; Fletcher, FE; Brown, VA; Stone, JR; Wilson, CB; Franklin, TH; Royal, CDM; Bonham, VL, Herstory as an Important Force in Bioethics., The Hastings Center report, vol. 52 Suppl 1 (March, 2022), pp. S83-S88 [doi]  [abs]
  6. Marshall, P; Royal, CDM; Chadwick, R, Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects., Public health genomics (January, 2022), pp. 1-8 [doi]  [abs]
  7. Wagner, JK; Yu, J-H; Chong, JX; Royal, CD; Bamshad, MJ, Centering Equity in Human Genetics and Genomics Advances., HGG advances, vol. 2 no. 4 (October, 2021), pp. 100048 [doi]
  8. Tukker, AM; Royal, CD; Bowman, AB; McAllister, KA, The Impact of Environmental Factors on Monogenic Mendelian Diseases., Toxicological sciences : an official journal of the Society of Toxicology, vol. 181 no. 1 (April, 2021), pp. 3-12 [doi]  [abs]
  9. Stewart, KA; Parshad-Asnani, M; Wonkam, A; Bollinger, J; Ngo Bitoungui, V; Wonkam-Tingang, E; Powell, J; Desronvil, K; Benson, KRK; Clark, A; Katz, M; Martin, B; Peterseim, C; Williams, C; Young, N; Shah, N; Tanabe, P; Babyak, M; Royal, CDM, "Pain is Subjective": A Mixed-Methods Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease Across Three Countries., J Pain Symptom Manage, vol. 61 no. 3 (March, 2021), pp. 474-487 [doi]  [abs]
  10. Royal, CDM; Babyak, M; Shah, N; Srivatsa, S; Stewart, KA; Tanabe, P; Wonkam, A; Asnani, M, Sickle cell disease is a global prototype for integrative research and healthcare., Adv Genet (Hoboken), vol. 2 no. 1 (March, 2021), pp. e10037, WILEY [doi]  [abs]
  11. Gyamfi, J; Ojo, T; Iwelunmor, J; Ogedegbe, G; Ryan, N; Diawara, A; Nnodu, O; Wonkam, A; Royal, C; Peprah, E, Implementation science research for the scale-up of evidence-based interventions for sickle cell disease in africa: a commentary., Globalization and health, vol. 17 no. 1 (February, 2021), pp. 20 [doi]  [abs]
  12. Teteh, DK; Dawkins-Moultin, L; Hooker, S; Hernandez, W; Bonilla, C; Galloway, D; LaGroon, V; Santos, ER; Shriver, M; Royal, CDM; Kittles, RA, Genetic ancestry, skin color and social attainment: The four cities study., PloS one, vol. 15 no. 8 (January, 2020), pp. e0237041 [doi]  [abs]
  13. Blanchard, JW; Outram, S; Tallbull, G; Royal, CDM, "We Don't Need a Swab in Our Mouth to Prove Who We Are": Identity, Resistance, and Adaptation of Genetic Ancestry Testing among Native American Communities., Current anthropology, vol. 60 no. 5 (October, 2019), pp. 637-655 [doi]  [abs]
  14. Bulgin, D; Tanabe, P; Asnani, M; Royal, CDM, Twelve tips for teaching a comprehensive disease-focused course with a global perspective: A sickle cell disease example., Medical teacher, vol. 41 no. 3 (March, 2019), pp. 275-281 [doi]  [abs]
  15. Sickle Cell Disease Ontology Working Group, , The Sickle Cell Disease Ontology: enabling universal sickle cell-based knowledge representation., Database : the journal of biological databases and curation, vol. 2019 (January, 2019), pp. baz118 [doi]  [abs]
  16. Callier, SL; Cunningham, BA; Powell, J; McDonald, MA; Royal, CDM, Cardiologists' Perspectives on Race-Based Drug Labels and Prescribing Within the Context of Treating Heart Failure., Health equity, vol. 3 no. 1 (January, 2019), pp. 246-253 [doi]  [abs]
  17. Baker, C; Powell, J; Le, D; Creary, MS; Daley, L-A; McDonald, MA; Royal, CD, Implementation of the NCAA Sickle Cell Trait Screening Policy: A Survey of Athletic Staff and Student-athletes., Journal of the National Medical Association, vol. 110 no. 6 (December, 2018), pp. 564-573 [doi]  [abs]
  18. Nelson, SC; Yu, J-H; Wagner, JK; Harrell, TM; Royal, CD; Bamshad, MJ, A content analysis of the views of genetics professionals on race, ancestry, and genetics., AJOB empirical bioethics, vol. 9 no. 4 (October, 2018), pp. 222-234 [doi]  [abs]
  19. Outram, S; Graves, JL; Powell, J; Wolpert, C; Haynie, KL; Foster, MW; Blanchard, JW; Hoffmeyer, A; Agans, RP; Royal, CD, Genes, Race, and Causation: US Public Perspectives About Racial Difference., Race and social problems, vol. 10 no. 2 (June, 2018), pp. 79-90 [doi]  [abs]
  20. Christensen, KD; Uhlmann, WR; Roberts, JS; Linnenbringer, E; Whitehouse, PJ; Royal, CDM; Obisesan, TO; Cupples, LA; Butson, MB; Fasaye, G-A; Hiraki, S; Chen, CA; Siebert, U; Cook-Deegan, R; Green, RC, A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone., Genetics in medicine : official journal of the American College of Medical Genetics, vol. 20 no. 1 (January, 2018), pp. 132-141 [doi]  [abs]
  21. McDonald, MA; Creary, MS; Powell, J; Daley, L-A; Baker, C; Royal, CD, Perspectives and Practices of Athletic Trainers and Team Physicians Implementing the 2010 NCAA Sickle Cell Trait Screening Policy., Journal of genetic counseling, vol. 26 no. 6 (December, 2017), pp. 1292-1300 [doi]  [abs]
  22. Ifekwunigwe, JO; Wagner, JK; Yu, J-H; Harrell, TM; Bamshad, MJ; Royal, CD, A Qualitative Analysis of How Anthropologists Interpret the Race Construct., American anthropologist, vol. 119 no. 3 (September, 2017), pp. 422-434 [doi]  [abs]
  23. Blanchard, JW; Tallbull, G; Wolpert, C; Powell, J; Foster, MW; Royal, C, Barriers and Strategies Related to Qualitative Research on Genetic Ancestry Testing in Indigenous Communities., Journal of empirical research on human research ethics : JERHRE, vol. 12 no. 3 (July, 2017), pp. 169-179 [doi]  [abs]
  24. Treadwell, MJ; Makani, J; Ohene-Frempong, K; Ofori-Acquah, S; McCurdy, S; De Vries, J; Bukini, D; Dennis-Antwi, J; Kamga, KK; Mbekenga, C; Wonkam, ET; Tangwa, G; Royal, CD; Wonkam, A, Stakeholder Perspectives on Public Health Genomics Applications for Sickle Cell Disease: A Methodology for a Human Heredity and Health in Africa (H3Africa) Qualitative Research Study, OMICS A Journal of Integrative Biology, vol. 21 no. 6 (June, 2017), pp. 323-332, MARY ANN LIEBERT, INC [doi]  [abs]
  25. Wagner, JK; Yu, J-H; Ifekwunigwe, JO; Harrell, TM; Bamshad, MJ; Royal, CD, Anthropologists' views on race, ancestry, and genetics., American journal of physical anthropology, vol. 162 no. 2 (February, 2017), pp. 318-327 [doi]  [abs]
  26. Mulder, N; Nembaware, V; Adekile, A; Anie, KA; Inusa, B; Brown, B; Campbell, A; Chinenere, F; Chunda-Liyoka, C; Derebail, VK; Geard, A; Ghedira, K; Hamilton, CM; Hanchard, NA; Haendel, M; Huggins, W; Ibrahim, M; Jupp, S; Kamga, KK; Knight-Madden, J; Lopez-Sall, P; Mbiyavanga, M; Munube, D; Nirenberg, D; Nnodu, O; Ofori-Acquah, SF; Ohene-Frempong, K; Opap, KB; Panji, S; Park, M; Pule, G; Royal, C; Sangeda, R; Tayo, B; Treadwell, M; Tshilolo, L; Wonkam, A, Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease, Applied & Translational Genomics, vol. 9 (June, 2016), pp. 23-29 [doi]  [abs]
  27. Bonham, VL; Callier, SL; Royal, CD, Will Precision Medicine Move Us beyond Race?, The New England journal of medicine, vol. 374 no. 21 (May, 2016), pp. 2003-2005 [doi]
  28. Christensen, KD; Roberts, JS; Whitehouse, PJ; Royal, CDM; Obisesan, TO; Cupples, LA; Vernarelli, JA; Bhatt, DL; Linnenbringer, E; Butson, MB; Fasaye, G-A; Uhlmann, WR; Hiraki, S; Wang, N; Cook-Deegan, R; Green, RC; REVEAL Study Group*, , Disclosing Pleiotropic Effects During Genetic Risk Assessment for Alzheimer Disease: A Randomized Trial., Annals of internal medicine, vol. 164 no. 3 (February, 2016), pp. 155-163, ISSN 0003-4819 [doi]  [abs]
  29. 1000 Genomes Project Consortium, ; Auton, A; Brooks, LD; Durbin, RM; Garrison, EP; Kang, HM; Korbel, JO; Marchini, JL; McCarthy, S; McVean, GA; Abecasis, GR, A global reference for human genetic variation., Nature, vol. 526 no. 7571 (October, 2015), pp. 68-74 [doi]  [abs]
  30. Green, RC; Christensen, KD; Cupples, LA; Relkin, NR; Whitehouse, PJ; Royal, CDM; Obisesan, TO; Cook-Deegan, R; Linnenbringer, E; Butson, MB; Fasaye, G-A; Levinson, E; Roberts, JS; REVEAL Study Group, , A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease., Alzheimer's & dementia : the journal of the Alzheimer's Association, vol. 11 no. 10 (October, 2015), pp. 1222-1230 [doi]  [abs]
  31. Wonkam, A; Makani, J; Ofori-Aquah, S; Nnodu, OE; Treadwell, M; Royal, C; Ohene-Frempong, K; Members of the H3Africa Consortium, , Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients., Cardiovascular journal of Africa, vol. 26 no. 2 Suppl 1 (March, 2015), pp. S50-S55 [doi]  [abs]
  32. Peprah, E; Xu, H; Tekola-Ayele, F; Royal, CD, Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease., Public health genomics, vol. 18 no. 1 (January, 2015), pp. 40-51 [doi]  [abs]
  33. Wonkam, A; de Vries, J; Royal, CD; Ramesar, R; Angwafo, FF, Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon., Journal of medical ethics, vol. 40 no. 9 (September, 2014), pp. 615-620, ISSN 0306-6800 [doi]  [abs]
  34. Delaneau, O; Marchini, J; 1000 Genomes Project Consortium, , Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel., Nature communications, vol. 5 (June, 2014), pp. 3934 [doi]  [abs]
  35. Colonna, V; Ayub, Q; Chen, Y; Pagani, L; Luisi, P; Pybus, M; Garrison, E; Xue, Y; Tyler-Smith, C; 1000 Genomes Project Consortium, ; Abecasis, GR; Auton, A; Brooks, LD; DePristo, MA; Durbin, RM; Handsaker, RE; Kang, HM; Marth, GT; McVean, GA, Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences., Genome biology, vol. 15 no. 6 (June, 2014), pp. R88 [doi]  [abs]
  36. Khurana, E; Fu, Y; Colonna, V; Mu, XJ; Kang, HM; Lappalainen, T; Sboner, A; Lochovsky, L; Chen, J; Harmanci, A; Das, J; Abyzov, A; Balasubramanian, S; Beal, K; Chakravarty, D; Challis, D; Chen, Y; Clarke, D; Clarke, L; Cunningham, F; Evani, US; Flicek, P; Fragoza, R; Garrison, E; Gibbs, R; Gümüş, ZH; Herrero, J; Kitabayashi, N; Kong, Y; Lage, K; Liluashvili, V; Lipkin, SM; MacArthur, DG; Marth, G; Muzny, D; Pers, TH; Ritchie, GRS; Rosenfeld, JA; Sisu, C; Wei, X; Wilson, M; Xue, Y; Yu, F; 1000 Genomes Project Consortium, ; Dermitzakis, ET; Yu, H; Rubin, MA; Tyler-Smith, C; Gerstein, M, Integrative annotation of variants from 1092 humans: application to cancer genomics., Science (New York, N.Y.), vol. 342 no. 6154 (October, 2013), pp. 1235587, ISSN 0036-8075 [doi]  [abs]
  37. Daley, L-AA; Wagner, JK; Himmel, TL; McPartland, KA; Katsanis, SH; Shriver, MD; Royal, CD, Personal DNA testing in college classrooms: perspectives of students and professors., edited by Kenneth I. Berns, Genetic testing and molecular biomarkers, vol. 17 no. 6 (June, 2013), pp. 446-452, Mary Ann Liebert, Inc. publishers, ISSN 1945-0265 [doi]  [abs]
  38. 1000 Genomes Project Consortium, ; Abecasis, GR; Auton, A; Brooks, LD; DePristo, MA; Durbin, RM; Handsaker, RE; Kang, HM; Marth, GT; McVean, GA, An integrated map of genetic variation from 1,092 human genomes., Nature, vol. 491 no. 7422 (November, 2012), pp. 56-65 [doi]  [abs]
  39. Jonassaint, CR; Ashley-Koch, A; Whitfield, KE; Hoyle, RH; Richman, LS; Siegler, IC; Royal, CD; Williams, R, The serotonin transporter gene polymorphism (5HTTLPR) moderates the effect of adolescent environmental conditions on self-esteem in young adulthood: a structural equation modeling approach., edited by O.V. Lipp, Biol Psychol, vol. 91 no. 1 (September, 2012), pp. 111-119, Elsevier, ISSN 0301-0511 [repository], [doi]  [abs]
  40. Wagner, JK; Royal, CD, Field of genes: an investigation of sports-related genetic testing., edited by Urs A. Meyer, Journal of personalized medicine, vol. 2 no. 3 (September, 2012), pp. 119-137, MDPI AG, ISSN 2075-4426 [available here], [doi]  [abs]
  41. Wagner, JK; Cooper, JD; Sterling, R; Royal, CD, Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests., edited by James Evans, Genetics in medicine : official journal of the American College of Medical Genetics, vol. 14 no. 6 (June, 2012), pp. 586-593, Nature Publishing Group, ISSN 1098-3600 [22382803], [doi]  [abs]
  42. Manswell Butty, J-A; Richardson, F; Mouton, CP; Royal, CDM; Green, RD; Munroe, K-A, Evaluation findings from genetics and family health history community-based workshops for African Americans., edited by JR Schmidtke, Journal of community genetics, vol. 3 no. 1 (January, 2012), pp. 1-12, Springer, ISSN 1868-310X [doi]  [abs]
  43. Akinleye, I; Roberts, JS; Royal, CDM; Linnenbringer, E; Obisesan, TO; Fasaye, G-A; Green, RC, Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease., Journal of genetic counseling, vol. 20 no. 6 (December, 2011), pp. 650-659, ISSN 1059-7700 [Gateway.cgi], [doi]  [abs]
  44. Royal, CDM, Genome-sequencing anniversary. My genome, my identity, my health., Science (New York, N.Y.), vol. 331 no. 6018 (February, 2011), pp. 690-691, ISSN 0036-8075 [Gateway.cgi], [doi]
  45. Rusert, BM; Royal, CDM, Grassroots marketing in a global era: more lessons from BiDil., The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics, vol. 39 no. 1 (January, 2011), pp. 79-90, ISSN 1073-1105 [Gateway.cgi], [doi]
  46. Royal, CD; Jonassaint, CR; Jonassaint, JC; De Castro, LM, Living with sickle cell disease: traversing 'race' and identity., Ethn Health, vol. 16 no. 4-5 (2011), pp. 389-404, ISSN 1355-7858 [doi]  [abs]
  47. Jonassaint, CR; Jonassaint, JC; Stanton, MV; De Castro, LM; Royal, CD, Clinical and sociodemographic factors predict coping styles among adults with sickle cell disease., J Natl Med Assoc, vol. 102 no. 11 (November, 2010), pp. 1045-1049, ISSN 1943-4693 [doi]  [abs]
  48. Jonassaint, CR; Santos, ER; Glover, CM; Payne, PW; Fasaye, G-A; Oji-Njideka, N; Hooker, S; Hernandez, W; Foster, MW; Kittles, RA; Royal, CD, Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry., Human genetics, vol. 128 no. 3 (September, 2010), pp. 249-260, ISSN 0340-6717 [doi]  [abs]
  49. International HapMap 3 Consortium, ; Altshuler, DM; Gibbs, RA; Peltonen, L; Dermitzakis, E; Schaffner, SF; Yu, F; Bonnen, PE; de Bakker, PIW; Deloukas, P; Gabriel, SB; Gwilliam, R; Hunt, S; Inouye, M; Jia, X; Palotie, A; Parkin, M; Whittaker, P; Chang, K; Hawes, A; Lewis, LR; Ren, Y; Wheeler, D; Muzny, DM; Barnes, C; Darvishi, K; Hurles, M; Korn, JM; Kristiansson, K; Lee, C; McCarrol, SA; Nemesh, J; Keinan, A; Montgomery, SB; Pollack, S; Price, AL; Soranzo, N; Gonzaga-Jauregui, C; Anttila, V; Brodeur, W; Daly, MJ; Leslie, S; McVean, G; Moutsianas, L; Nguyen, H; Zhang, Q; Ghori, MJR; McGinnis, R; McLaren, W; Takeuchi, F; Grossman, SR; Shlyakhter, I; Hostetter, EB; Sabeti, PC; Adebamowo, CA; Foster, MW; Gordon, DR; Licinio, J; Manca, MC; Marshall, PA; Matsuda, I; Ngare, D; Wang, VO; Reddy, D; Rotimi, CN; Royal, CD; Sharp, RR; Zeng, C; Brooks, LD; McEwen, JE, Integrating common and rare genetic variation in diverse human populations., Nature, vol. 467 no. 7311 (September, 2010), pp. 52-58, ISSN 0028-0836 [doi]  [abs]
  50. Sirugo, G; Williams, SM; Royal, CDM; Newport, MJ; Hennig, BJ; Mariani-Costantini, R; Buonaguro, FM; Velez Edwards, DR; Ibrahim, M; Soodyall, H; Wonkam, A; Ramesar, R; Rotimi, CN, Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon., The American journal of tropical medicine and hygiene, vol. 83 no. 2 (August, 2010), pp. 226-229 [doi]  [abs]
  51. Royal, CD; Novembre, J; Fullerton, SM; Goldstein, DB; Long, JC; Bamshad, MJ; Clark, AG, Inferring genetic ancestry: opportunities, challenges, and implications., American journal of human genetics, vol. 86 no. 5 (May, 2010), pp. 661-673, ISSN 0002-9297 [doi]  [abs]
  52. Darity, W; Royal, C; Whitfield, K, Race, genetics and health: An introduction, Review of Black Political Economy, vol. 37 no. 1 (January, 2010), pp. 1-6, SAGE Publications [doi]  [abs]
  53. Madhere, S; Harrell, J; Royal, CDM, Social Ecology, Genomics, and African American Health: A Nonlinear Dynamical Perspective., The Journal of black psychology, vol. 35 no. 2 (January, 2009), pp. 154-179, ISSN 0095-7984 [Gateway.cgi], [doi]  [abs]
  54. Christensen, KD; Roberts, JS; Royal, CDM; Fasaye, G-A; Obisesan, T; Cupples, LA; Whitehouse, PJ; Butson, MB; Linnenbringer, E; Relkin, NR; Farrer, L; Cook-Deegan, R; Green, RC, Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience., Genetics in medicine : official journal of the American College of Medical Genetics, vol. 10 no. 3 (March, 2008), pp. 207-214, ISSN 1098-3600 [doi]  [abs]
  55. Sabeti, PC; Varilly, P; Fry, B; Lohmueller, J; Hostetter, E; Cotsapas, C; Xie, X; Byrne, EH; McCarroll, SA; Gaudet, R; Schaffner, SF; Lander, ES; International HapMap Consortium, ; Frazer, KA; Ballinger, DG; Cox, DR; Hinds, DA; Stuve, LL; Gibbs, RA; Belmont, JW; Boudreau, A; Hardenbol, P; Leal, SM; Pasternak, S; Wheeler, DA; Willis, TD; Yu, F; Yang, H; Zeng, C; Gao, Y; Hu, H; Hu, W; Li, C; Lin, W; Liu, S; Pan, H; Tang, X; Wang, J; Wang, W; Yu, J; Zhang, B; Zhang, Q; Zhao, H; Zhao, H; Zhou, J; Gabriel, SB; Barry, R; Blumenstiel, B; Camargo, A; Defelice, M; Faggart, M; Goyette, M; Gupta, S; Moore, J; Nguyen, H; Onofrio, RC; Parkin, M; Roy, J; Stahl, E; Winchester, E; Ziaugra, L; Altshuler, D; Shen, Y; Yao, Z; Huang, W; Chu, X; He, Y; Jin, L; Liu, Y; Shen, Y; Sun, W; Wang, H; Wang, Y; Wang, Y; Xiong, X; Xu, L; Waye, MMY; Tsui, SKW; Xue, H; Wong, JT-F; Galver, LM; Fan, J-B; Gunderson, K; Murray, SS; Oliphant, AR; Chee, MS; Montpetit, A; Chagnon, F; Ferretti, V; Leboeuf, M; Olivier, J-F; Phillips, MS; Roumy, S; Sallée, C; Verner, A; Hudson, TJ; Kwok, P-Y; Cai, D; Koboldt, DC; Miller, RD; Pawlikowska, L; Taillon-Miller, P; Xiao, M; Tsui, L-C; Mak, W; Song, YQ; Tam, PKH; Nakamura, Y; Kawaguchi, T; Kitamoto, T; Morizono, T; Nagashima, A; Ohnishi, Y; Sekine, A; Tanaka, T; Tsunoda, T; Deloukas, P; Bird, CP; Delgado, M; Dermitzakis, ET; Gwilliam, R; Hunt, S; Morrison, J; Powell, D; Stranger, BE; Whittaker, P; Bentley, DR; Daly, MJ; de Bakker, PIW; Barrett, J; Chretien, YR; Maller, J; McCarroll, S; Patterson, N; Pe'er, I; Price, A; Purcell, S; Richter, DJ; Sabeti, P; Saxena, R; Sham, PC; Stein, LD; Krishnan, L; Smith, AV; Tello-Ruiz, MK; Thorisson, GA; Chakravarti, A; Chen, PE; Cutler, DJ; Kashuk, CS; Lin, S; Abecasis, GR; Guan, W; Li, Y; Munro, HM; Qin, ZS; Thomas, DJ; McVean, G; Auton, A; Bottolo, L; Cardin, N; Eyheramendy, S; Freeman, C; Marchini, J; Myers, S; Spencer, C; Stephens, M; Donnelly, P; Cardon, LR; Clarke, G; Evans, DM; Morris, AP; Weir, BS; Johnson, TA; Mullikin, JC; Sherry, ST; Feolo, M; Skol, A; Zhang, H; Matsuda, I; Fukushima, Y; Macer, DR; Suda, E; Rotimi, CN; Adebamowo, CA; Ajayi, I; Aniagwu, T; Marshall, PA; Nkwodimmah, C; Royal, CDM; Leppert, MF; Dixon, M; Peiffer, A; Qiu, R; Kent, A; Kato, K; Niikawa, N; Adewole, IF; Knoppers, BM; Foster, MW; Clayton, EW; Watkin, J; Muzny, D; Nazareth, L; Sodergren, E; Weinstock, GM; Yakub, I; Birren, BW; Wilson, RK; Fulton, LL; Rogers, J; Burton, J; Carter, NP; Clee, CM; Griffiths, M; Jones, MC; McLay, K; Plumb, RW; Ross, MT; Sims, SK; Willey, DL; Chen, Z; Han, H; Kang, L; Godbout, M; Wallenburg, JC; L'Archevêque, P; Bellemare, G; Saeki, K; Wang, H; An, D; Fu, H; Li, Q; Wang, Z; Wang, R; Holden, AL; Brooks, LD; McEwen, JE; Guyer, MS; Wang, VO; Peterson, JL; Shi, M; Spiegel, J; Sung, LM; Zacharia, LF; Collins, FS; Kennedy, K; Jamieson, R; Stewart, J, Genome-wide detection and characterization of positive selection in human populations., Nature, vol. 449 no. 7164 (October, 2007), pp. 913-918 [doi]  [abs]
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  59. Rotimi, C; Leppert, M; Matsuda, I; Zeng, C; Zhang, H; Adebamowo, C; Ajayi, I; Aniagwu, T; Dixon, M; Fukushima, Y; Macer, D; Marshall, P; Nkwodimmah, C; Peiffer, A; Royal, C; Suda, E; Zhao, H; Wang, VO; McEwen, J; International HapMap Consortium, , Community engagement and informed consent in the International HapMap project., Community genetics, vol. 10 no. 3 (January, 2007), pp. 186-198 [doi]  [abs]
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  62. Foster, MW; Royal, CDM; Sharp, RR, The routinisation of genomics and genetics: implications for ethical practices., Journal of medical ethics, vol. 32 no. 11 (November, 2006), pp. 635-638, ISSN 0306-6800 [Gateway.cgi], [doi]  [abs]
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  65. International HapMap Consortium, , A haplotype map of the human genome., Nature, vol. 437 no. 7063 (October, 2005), pp. 1299-1320, Springer Nature, ISSN 0028-0836 [Gateway.cgi], [doi]  [abs]
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  69. Royal, CDM; Dunston, G, The Human Genome: Implications for the Health of African Americans, in Praeger handbook of Black American health, edited by Livingston, IL (June, 2004), pp. 757-775, Praeger Publishers, ISBN 9780313332210
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  76. Weinrich, S; Royal, C; Pettaway, CA; Dunston, G; Faison-Smith, L; Priest, JH; Roberson-Smith, P; Frost, J; Jenkins, J; Brooks, KA; Powell, I, Interest in genetic prostate cancer susceptibility testing among african American men., Cancer nursing, vol. 25 no. 1 (February, 2002), pp. 28-34 [doi]  [abs]
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  79. Ellison, GL; Coker, AL; Hebert, JR; Sanderson, SM; Royal, CD; Weinrich, SP, Psychosocial stress and prostate cancer: a theoretical model., Ethnicity & disease, vol. 11 no. 3 (January, 2001), pp. 484-495  [abs]
  80. Royal, C; Baffoe-Bonnie, A; Kittles, R; Powell, I; Bennett, J; Hoke, G; Pettaway, C; Weinrich, S; Vijayakumar, S; Ahaghotu, C; Mason, T; Johnson, E; Obeikwe, M; Simpson, C; Mejia, R; Boykin, W; Roberson, P; Frost, J; Faison-Smith, L; Meegan, C; Foster, N; Furbert-Harris, P; Carpten, J; Bailey-Wilson, J; Trent, J; Berg, K; Dunston, G; Collins, F, Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study., Annals of epidemiology, vol. 10 no. 8 Suppl (November, 2000), pp. S68-S77 [doi]  [abs]
  81. Royal, CD; Headings, VE; Harrell, JP; Ampy, FR; Hall, GW, Coping strategies in families of children with sickle cell disease., Ethnicity & disease, vol. 10 no. 2 (March, 2000), pp. 237-247  [abs]
  82. Royal, CD; Headings, VE; Molnar, ET; Ampy, FR, Resilience in siblings of children with sickle cell disease., Journal of genetic counseling, vol. 4 no. 3 (September, 1995), pp. 199-217 [doi]  [abs]

Willard, Huntington F.

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  17. Earnshaw, WC and Allshire, RC and Black, BE and Bloom, K and Brinkley, BR and Brown, W and Cheeseman, IM and Choo, KHA and Copenhaver, GP and Deluca, JG and Desai, A and Diekmann, S and Erhardt, S and Fitzgerald-Hayes, M and Foltz, D and Fukagawa, T and Gassmann, R and Gerlich, DW and Glover, DM and Gorbsky, GJ and Harrison, SC and Heun, P and Hirota, T and Jansen, LET and Karpen, G and Kops, GJPL and Lampson, MA and Lens, SM and Losada, A and Luger, K and Maiato, H and Maddox, PS and Margolis, RL and Masumoto, H and McAinsh, AD and Mellone, BG and Meraldi, P and Musacchio, A and Oegema, K and O'Neill, RJ and Salmon, ED and Scott, KC and Straight, AF and Stukenberg, PT and Sullivan, BA and Sullivan, KF and Sunkel, CE and Swedlow, JR and Walczak, CE and Warburton, PE and Westermann, S and Willard, HF and Wordeman, L and Yanagida, M and Yen, TJ and Yoda, K and Cleveland, DW, Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant, Chromosome Research, vol. 21 (2013), pp. 101--106, ISSN 0967-3849 [doi]  [abs]
  18. Reddy, TE; Gertz, J; Pauli, F; Kucera, KS; Varley, KE; Newberry, KM; Marinov, GK; Mortazavi, A; Williams, BA; Song, L; Crawford, GE; Wold, B; Willard, HF; Myers, RM, Effects of sequence variation on differential allelic transcription factor occupancy and gene expression., Genome research, vol. 22 no. 5 (May, 2012), pp. 860-869 [22300769], [doi]  [abs]
  19. Reddy, TE and Gertz, J and Pauli, F and Kucera, KS and Varley, KE and Newberry, KM and Marinov, GK and Mortazavi, A and Williams, BA and Song, L and Crawford, GE and Wold, B and Willard, HF and Myers, RM, Effects of sequence variation on differential allelic transcription factor occupancy and gene expression., Genome Res, vol. 22 (May, 2012), pp. 860--869 [22300769], [doi]  [abs]
  20. Wheeler, BS; Ruderman, BT; Willard, HF; Scott, KC, Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast., Genetics, vol. 190 no. 2 (February, 2012), pp. 549-557 [22143918], [doi]  [abs]
  21. Wheeler, BS and Ruderman, BT and Willard, HF and Scott, KC, Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast., Genetics, vol. 190 (February, 2012), pp. 549--557 [22143918], [doi]  [abs]
  22. Hayden, KE and Willard, HF, Composition and organization of active centromere sequences in complex genomes., BMC Genomics, vol. 13 (2012), pp. 324 [22817545], [doi]  [abs]
  23. Wang, Z and Willard, HF, Evidence for sequence biases associated with patterns of histone methylation., BMC Genomics, vol. 13 (2012), pp. 367 [22857523], [doi]  [abs]
  24. Thorvaldsen, JL and Krapp, C and Willard, HF and Bartolomei, MS, Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome, Genetics, vol. 192 (2012), pp. 1095--1107, ISSN 0016-6731 [doi]  [abs]
  25. Hayden, KE; Willard, HF, Composition and organization of active centromere sequences in complex genomes., BMC Genomics, vol. 13 (2012), pp. 324 [22817545], [doi]  [abs]
  26. Wang, Z; Willard, HF, Evidence for sequence biases associated with patterns of histone methylation., BMC Genomics, vol. 13 (2012), pp. 367 [22857523], [doi]  [abs]
  27. Thorvaldsen, JL; Krapp, C; Willard, HF; Bartolomei, MS, Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome, Genetics, vol. 192 no. 3 (2012), pp. 1095-1107, ISSN 0016-6731 [doi]  [abs]
  28. Kucera, KS; Reddy, TE; Pauli, F; Gertz, J; Logan, JE; Myers, RM; Willard, HF, Allele-specific distribution of RNA polymerase II on female X chromosomes., Human Molecular Genetics, vol. 20 no. 20 (October, 2011), pp. 3964-3973 [21791549], [doi]  [abs]
  29. Kucera, KS and Reddy, TE and Pauli, F and Gertz, J and Logan, JE and Myers, RM and Willard, HF, Allele-specific distribution of RNA polymerase II on female X chromosomes., Hum Mol Genet, vol. 20 (October, 2011), pp. 3964--3973 [21791549], [doi]  [abs]
  30. Horvath, JE; Sheedy, CB; Merrett, SL; Diallo, AB; Swofford, DL; NISC Comparative Sequencing Program, ; Green, ED; Willard, HF, Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus., Genome research, vol. 21 no. 6 (June, 2011), pp. 850-862 [21518738], [doi]  [abs]
  31. Horvath, JE and Sheedy, CB and Merrett, SL and Diallo, AB and Swofford, DL and NISC Comparative Sequencing Program and Green, ED and Willard, HF, Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus., Genome Res, vol. 21 (June, 2011), pp. 850--862 [21518738], [doi]  [abs]
  32. Gertz, J and Varley, KE and Reddy, TE and Bowling, KM and Pauli, F and Parker, SL and Kucera, KS and Willard, HF and Myers, RM, Analysis of dna methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation, PLoS Genetics, vol. 7 (2011), ISSN 1553-7390 [doi]  [abs]
  33. Lee, HR and Hayden, KE and Willard, HF, Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome., Genome Biol Evol, vol. 3 (2011), pp. 1136--1149 [21828373], [doi]  [abs]
  34. Anderson, WA and Amasino, RM and Jr, MA and Banerjee, U and Bartel, B and Corces, VG and Drennan, CL and Elgin, SCR and Epstein, IR and Fanning, E and Jr, LJG and Handelsman, JO and Hatfull, GF and Hoy, RR and Kelley, D and Leinwand, LA and Losick, R and Lu, Y and Lynn, DG and Neuhauser, C and O'Dowd, DK and Olivera, T and Pevzner, P and Richards-Kortum, RR and Rine, J and Sah, RL and Strobel, SA and Walker, GC and Walt, DR and Warner, IM and Wessler, S and Willard, HF and Zare, RN, Competencies: A cure for pre-med curriculum, Science, vol. 334 (2011), pp. 760--761, ISSN 0036-8075 [doi]
  35. Lee, HR; Hayden, KE; Willard, HF, Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome., Genome Biology and Evolution, vol. 3 (2011), pp. 1136-1149 [21828373], [doi]  [abs]
  36. Gertz, J; Varley, KE; Reddy, TE; Bowling, KM; Pauli, F; Parker, SL; Kucera, KS; Willard, HF; Myers, RM, Analysis of dna methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation, PLoS genetics, vol. 7 no. 8 (2011), ISSN 1553-7390 [doi]  [abs]
  37. McDaniell, R and Lee, BK and Song, L and Liu, Z and Boyle, AP and Erdos, MR and Scott, LJ and Morken, MA and Kucera, KS and Battenhouse, A and Keefe, D and Collins, FS and Willard, HF and Lieb, JD and Furey, TS and Crawford, GE and Iyer, VR and Birney, E, Heritable individual-specific and allele-specific chromatin signatures in humans., Science, vol. 328 (April, 2010), pp. 235--239 [20299549], [doi]  [abs]
  38. Willard, HF, ASHG Awards and Addresses. 2009 William Allan Award address: Life in the sandbox: unfinished business., The American Journal of Human Genetics, vol. 86 no. 3 (March, 2010), pp. 318-327 [20529654], [doi]
  39. Ginsburg, GS and Willard, HF, The Foundations of Genomic and Personalized Medicine, Essentials of Genomic and Personalized Medicine (2010), pp. 1--10 [doi]  [abs]
  40. Ginsburg, GS and Willard, HF, Preface, Essentials of Genomic and Personalized Medicine (2010), pp. ix--ix [doi]
  41. Willard, HF, Organization, Variation and Expression of the Human Genome, Essentials of Genomic and Personalized Medicine (2010), pp. 13--26 [doi]  [abs]
  42. Wheeler, BS and Blau, JA and Willard, HF and Scott, KC, The impact of local genome sequence on defining heterochromatin domains., PLoS Genet, vol. 5 (April, 2009), pp. e1000453 [19360117], [doi]  [abs]
  43. Willard, HF, Organization, Variation and Expression of the Human Genome as a Foundation of Genomic and Personalized Medicine, Genomic and Personalized Medicine, Two-Vol Set (2009), pp. 1--21 [doi]
  44. Willard, HF and Ginsburg, GS, Preface, Genomic and Personalized Medicine, Two-Vol Set (2009), pp. xxvii--xxviii
  45. Ginsburg, GS and Willard, HF, Genomic and Personalized Medicine, Two-Vol Set, Genomic and Personalized Medicine, Two-Vol Set (2009)  [abs]
  46. Kawamoto, K and Lobach, DF and Willard, HF and Ginsburg, GS, A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine., BMC Med Inform Decis Mak, vol. 9 (2009), pp. 17 [19309514], [doi]  [abs]
  47. Horvath, JE and Weisrock, DW and Embry, SL and Fiorentino, I and Balhoff, JP and Kappeler, P and Wray, GA and Willard, HF and Yoder, AD, Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs., Genome Res, vol. 18 (March, 2008), pp. 489--499, ISSN 1088-9051 [18245770], [doi]  [abs]
  48. Haga, SB and Willard, HF, Letting the genome out of the bottle, New England Journal of Medicine, vol. 358 (2008), pp. 2184-, ISSN 0028-4793 [doi]
  49. Willard, HF, Avoid boring people: And other lessons from a life in science, Nature, vol. 449 no. 7164 (October, 2007), pp. 787-787, ISSN 0028-0836 [Gateway.cgi], [doi]
  50. Horvath, JE and Willard, HF, Primate comparative genomics: lemur biology and evolution., Trends Genet, vol. 23 (April, 2007), pp. 173--182, ISSN 0168-9525 [17331617], [doi]  [abs]
  51. Basu, J and Willard, HF and Stromberg, G, Human artificial chromosome assembly by transposon-based retrofitting of genomic BACs with synthetic alpha-satellite arrays., Curr Protoc Hum Genet, vol. Chapter 5 (January, 2007), pp. Unit--5.18 [18428412], [doi]  [abs]
  52. Scott, KC and White, CV and Willard, HF, An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1., PLoS One, vol. 2 (2007), pp. e1099 [17971862], [doi]  [abs]
  53. Haga, SB and Willard, HF, Defining the spectrum of genome policy., Nat Rev Genet, vol. 7 (December, 2006), pp. 966--972, ISSN 1471-0056 [17139328], [doi]  [abs]
  54. Basu, J and Willard, HF, Human artificial chromosomes: potential applications and clinical considerations., Pediatr Clin North Am, vol. 53 (October, 2006), pp. 843--viii, ISSN 0031-3955 [17027613], [doi]  [abs]
  55. Wang, Z and Willard, HF and Mukherjee, S and Furey, TS, Evidence of influence of genomic DNA sequence on human X chromosome inactivation., PLoS Comput Biol, vol. 2 (September, 2006), pp. e113 [16948528], [doi]  [abs]
  56. Chadwick, LH and Pertz, LM and Broman, KW and Bartolomei, MS and Willard, HF, Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval., Genetics, vol. 173 (August, 2006), pp. 2103--2110, ISSN 0016-6731 [16582439], [doi]  [abs]
  57. Valley, CM and Pertz, LM and Balakumaran, BS and Willard, HF, Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome., Hum Mol Genet, vol. 15 (August, 2006), pp. 2335--2347, ISSN 0964-6906 [16787966], [doi]  [abs]
  58. Valley, CM and Willard, HF, Genomic and epigenomic approaches to the study of X chromosome inactivation., Curr Opin Genet Dev, vol. 16 (June, 2006), pp. 240--245, ISSN 0959-437X [16647845], [doi]  [abs]
  59. Rudd, MK and Wray, GA and Willard, HF, The evolutionary dynamics of alpha-satellite., Genome Res, vol. 16 (January, 2006), pp. 88--96, ISSN 1088-9051 [16344556], [doi]  [abs]
  60. Scott, KC and Merrett, SL and Willard, HF, A heterochromatin barrier partitions the fission yeast centromere into discrete chromatin domains., Curr Biol, vol. 16 (January, 2006), pp. 119--129, ISSN 0960-9822 [16431364], [doi]  [abs]
  61. Shianna, KV and Willard, HF, Human genomics: In search of normality, Nature, vol. 444 (2006), pp. 428--429, ISSN 0028-0836 [doi]  [abs]
  62. Willard, HE and Rudd, MK, Genomic organization and function of human centromeres, Genomic Disorders: The Genomic Basis of Disease (2006), pp. 115--129 [doi]  [abs]
  63. Amos-Landgraf, JM and Cottle, A and Plenge, RM and Friez, M and Schwartz, CE and Longshore, J and Willard, HF, X chromosome-inactivation patterns of 1,005 phenotypically unaffected females, American Journal of Human Genetics, vol. 79 (2006), pp. 493--499, ISSN 0002-9297 [doi]  [abs]
  64. Wang, Z; Willard, HF; Mukherjee, S; Furey, TS, Evidence of Influence of Genomic DNA Sequence on Human X Chromosome Inactivation., PLoS Computational Biology, vol. 2 no. 9 (2006) [doi]
  65. Chadwick, LH and Willard, HF, Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice., Mamm Genome, vol. 16 (September, 2005), pp. 691--699, ISSN 0938-8990 [16245026], [doi]  [abs]
  66. Willard, HF and Angrist, M and Ginsburg, GS, Genomic medicine: genetic variation and its impact on the future of health care., Philos Trans R Soc Lond B Biol Sci, vol. 360 (August, 2005), pp. 1543--1550, ISSN 0962-8436 [16096102], [doi]  [abs]
  67. Basu, J and Willard, HF, Artificial and engineered chromosomes: non-integrating vectors for gene therapy., Trends Mol Med, vol. 11 (May, 2005), pp. 251--258, ISSN 1471-4914 [15882613], [doi]  [abs]
  68. Ross, MT and Grafham, DV and Coffey, AJ and Scherer, S and McLay, K and Muzny, D and Platzer, M and Howell, GR and Burrows, C and Bird, CP and Frankish, A and Lovell, FL and Howe, KL and Ashurst, JL and Fulton, RS and Sudbrak, R and Wen, G and Jones, MC and Hurles, ME and Andrews, TD and Scott, CE and Searle, S and Ramser, J and Whittaker, A and Deadman, R and Carter, NP and Hunt, SE and Chen, R and Cree, A and Gunaratne, P and Havlak, P and Hodgson, A and Metzker, ML and Richards, S and Scott, G and Steffen, D and Sodergren, E and Wheeler, DA and Worley, KC and Ainscough, R and Ambrose, KD and Ansari-Lari, MA and Aradhya, S and Ashwell, RI and Babbage, AK and Bagguley, CL and Ballabio, A and Banerjee, R and Barker, GE and Barlow, KF and Barrett, IP and Bates, KN and Beare, DM and Beasley, H and Beasley, O and Beck, A and Bethel, G and Blechschmidt, K and Brady, N and Bray-Allen, S and Bridgeman, AM and Brown, AJ and Brown, MJ and Bonnin, D and Bruford, EA and Buhay, C and Burch, P and Burford, D and Burgess, J and Burrill, W and Burton, J and Bye, JM and Carder, C and Carrel, L and Chako, J and Chapman, JC and Chavez, D and Chen, E and Chen, G and Chen, Y and Chen, Z and Chinault, C and Ciccodicola, A and Clark, SY and Clarke, G and Clee, CM and Clegg, S and Clerc-Blankenburg, K and Clifford, K and Cobley, V and Cole, CG and Conquer, JS and Corby, N and Connor, RE and David, R and Davies, J and Davis, C and Davis, J and Delgado, O and Deshazo, D and Dhami, P and Ding, Y and Dinh, H and Dodsworth, S and Draper, H and Dugan-Rocha, S and Dunham, A and Dunn, M and Durbin, KJ and Dutta, I and Eades, T and Ellwood, M and Emery-Cohen, A and Errington, H and Evans, KL and Faulkner, L and Francis, F and Frankland, J and Fraser, AE and Galgoczy, P and Gilbert, J and Gill, R and Glöckner, G and Gregory, SG and Gribble, S and Griffiths, C and Grocock, R and Gu, Y and Gwilliam, R and Hamilton, C and Hart, EA and Hawes, A and Heath, PD and Heitmann, K and Hennig, S and Hernandez, J and Hinzmann, B and Ho, S and Hoffs, M and Howden, PJ and Huckle, EJ and Hume, J and Hunt, PJ and Hunt, AR and Isherwood, J and Jacob, L and Johnson, D and Jones, S and de Jong, PJ and Joseph, SS and Keenan, S and Kelly, S and Kershaw, JK and Khan, Z and Kioschis, P and Klages, S and Knights, AJ and Kosiura, A and Kovar-Smith, C and Laird, GK and Langford, C and Lawlor, S and Leversha, M and Lewis, L and Liu, W and Lloyd, C and Lloyd, DM and Loulseged, H and Loveland, JE and Lovell, JD and Lozado, R and Lu, J and Lyne, R and Ma, J and Maheshwari, M and Matthews, LH and McDowall, J and McLaren, S and McMurray, A and Meidl, P and Meitinger, T and Milne, S and Miner, G and Mistry, SL and Morgan, M and Morris, S and Müller, I and Mullikin, JC and Nguyen, N and Nordsiek, G and Nyakatura, G and O'Dell, CN and Okwuonu, G and Palmer, S and Pandian, R and Parker, D and Parrish, J and Pasternak, S and Patel, D and Pearce, AV and Pearson, DM and Pelan, SE and Perez, L and Porter, KM and Ramsey, Y and Reichwald, K and Rhodes, S and Ridler, KA and Schlessinger, D and Schueler, MG and Sehra, HK and Shaw-Smith, C and Shen, H and Sheridan, EM and Shownkeen, R and Skuce, CD and Smith, ML and Sotheran, EC and Steingruber, HE and Steward, CA and Storey, R and Swann, RM and Swarbreck, D and Tabor, PE and Taudien, S and Taylor, T and Teague, B and Thomas, K and Thorpe, A and Timms, K and Tracey, A and Trevanion, S and Tromans, AC and d'Urso, M and Verduzco, D and Villasana, D and Waldron, L and Wall, M and Wang, Q and Warren, J and Warry, GL and Wei, X and West, A and Whitehead, SL and Whiteley, MN and Wilkinson, JE and Willey, DL and Williams, G and Williams, L and Williamson, A and Williamson, H and Wilming, L and Woodmansey, RL and Wray, PW and Yen, J and Zhang, J and Zhou, J and Zoghbi, H and Zorilla, S and Buck, D and Reinhardt, R and Poustka, A and Rosenthal, A and Lehrach, H and Meindl, A and Minx, PJ and Hillier, LW and Willard, HF and Wilson, RK and Waterston, RH and Rice, CM and Vaudin, M and Coulson, A and Nelson, DL and Weinstock, G and Sulston, JE and Durbin, R and Hubbard, T and Gibbs, RA and Beck, S and Rogers, J and Bentley, DR, The DNA sequence of the human X chromosome., Nature, vol. 434 (March, 2005), pp. 325--337 [15772651], [doi]  [abs]
  69. Basu, J and Stromberg, G and Compitello, G and Willard, HF and Bokkelen, GV, Erratum: Rapid creation of BAC-based human artifical chromosome vectors by transposition with synthetic alpha-satellite arrays (Nucleic Acids Research (2005) vol. 33 (587-596)), Nucleic Acids Research, vol. 33 (2005), pp. 1421--1422, ISSN 0305-1048 [doi]
  70. Carrel, L and Willard, HF, X-inactivation profile reveals extensive variability in X-linked gene expression in females, Nature, vol. 434 (2005), pp. 400--404 [doi]  [abs]
  71. Higgins, AW and Gustashaw, KM and Willard, HF, Engineered human dicentric chromosomes show centromere plasticity, Chromosome Research, vol. 13 (2005), pp. 745--762, ISSN 0967-3849 [doi]  [abs]
  72. Basu, J and Compitello, G and Stromberg, G and Willard, HF and Van Bokkelen, G, Efficient assembly of de novo human artificial chromosomes from large genomic loci., BMC Biotechnol, vol. 5 (2005), pp. 21 [15998466], [doi]  [abs]
  73. Basu, J and Stromberg, G and Compitello, G and Willard, HF and Van Bokkelen, G, Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays., Nucleic Acids Res, vol. 33 (2005), pp. 587--596 [15673719], [doi]  [abs]
  74. Schueler, MG and Dunn, JM and Bird, CP and Ross, MT and Viggiano, L and Rocchi, M and Willard, HF and Green, ED, Progressive proximal expansion of the primate X chromosome centromere, Proceedings of the National Academy of Sciences of the United States of America, vol. 102 (2005), pp. 10563--10568, ISSN 0027-8424 [doi]  [abs]
  75. J Basu, G Stromberg, G Compitello, HF Willard, G Van Bokkelen, Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays., Nucleic acids research, vol. 33 no. 2 (2005), pp. 587-96, ISSN 1362-4962 [doi]  [abs]
  76. BP Chadwick, HF Willard, Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome., Proceedings of the National Academy of Sciences of the United States of America, vol. 101 no. 50 (December, 2004), pp. 17450-5, ISSN 0027-8424 [doi]  [abs]
  77. Chadwick, BP and Willard, HF, Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome., Proc Natl Acad Sci U S A, vol. 101 (December, 2004), pp. 17450--17455, ISSN 0027-8424 [15574503], [doi]  [abs]
  78. MK Rudd, HF Willard, Analysis of the centromeric regions of the human genome assembly., Trends in genetics : TIG, vol. 20 no. 11 (November, 2004), pp. 529-33, ISSN 0168-9525 [doi]  [abs]
  79. Rudd, MK and Willard, HF, Analysis of the centromeric regions of the human genome assembly., Trends Genet, vol. 20 (November, 2004), pp. 529--533, ISSN 0168-9525 [15475110], [doi]  [abs]
  80. Grimes, BR and Babcock, J and Rudd, MK and Chadwick, B and Willard, HF, Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes., Genome Biol, vol. 5 (2004), pp. R89 [15535865], [doi]  [abs]
  81. Willard, HF, Introductory Speech for David Page, American Journal of Human Genetics, vol. 74 (2004), pp. 397--398 [doi]
  82. Baltimore, D and Nossal, G and Navratil, G and Daley, G and Barakat, R and Kay, M and Daley, G and Friedman, L and Buick, R and Trautmann, A and Sharav, V and Stein, J and Rahmstorf, S and Rapley, C and Collins, F and Fauci, A and Clarke, AC and Tam, P and Willard, H, New Year's wishes: All I want for 2005 is..., Nature, vol. 432 (2004), pp. 942--948, ISSN 0028-0836 [doi]
  83. BR Grimes, J Babcock, MK Rudd, B Chadwick, HF Willard, Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes., Genome biology, vol. 5 no. 11 (2004), pp. R89, ISSN 1465-6914 [doi]  [abs]
  84. BP Chadwick, HF Willard, Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X., Seminars in cell & developmental biology, England, vol. 14 no. 6 (December, 2003), pp. 359-67, ISSN 1084-9521  [abs]
  85. Chadwick, BP and Willard, HF, Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X., Semin Cell Dev Biol, vol. 14 (December, 2003), pp. 359--367, ISSN 1084-9521 [15015743]  [abs]
  86. MK Rudd, RW Mays, S Schwartz, HF Willard, Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag., Molecular and cellular biology, United States, vol. 23 no. 21 (November, 2003), pp. 7689-97, ISSN 0270-7306  [abs]
  87. Rudd, MK and Mays, RW and Schwartz, S and Willard, HF, Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag., Mol Cell Biol, vol. 23 (November, 2003), pp. 7689--7697, ISSN 0270-7306 [14560014]  [abs]
  88. Carrel, L; Nickel, G; Trevarthen, K; Dunn, J; Willard, HF, A comprehensive X inactivation profile of the human X chromosome., The American Journal of Human Genetics, vol. 73 no. 5 (November, 2003), pp. 180-180, ISSN 0002-9297 [Gateway.cgi]
  89. Rudd, K; Dunn, J; Willard, HF, Functional and evolutionary annotation of the chromosome 17 centromere., The American Journal of Human Genetics, vol. 73 no. 5 (November, 2003), pp. 217-217, ISSN 0002-9297 [Gateway.cgi]
  90. BP Chadwick, HF Willard, Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome., Human molecular genetics, vol. 12 no. 17 (September, 2003), pp. 2167-78, ISSN 0964-6906 [doi]  [abs]
  91. Chadwick, BP and Willard, HF, Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome., Hum Mol Genet, vol. 12 (September, 2003), pp. 2167--2178, ISSN 0964-6906 [12915472], [doi]  [abs]
  92. I Percec, JL Thorvaldsen, RM Plenge, CJ Krapp, JH Nadeau, HF Willard, MS Bartolomei, An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse., Genetics, vol. 164 no. 4 (August, 2003), pp. 1481-94, ISSN 0016-6731  [abs]
  93. Percec, I and Thorvaldsen, JL and Plenge, RM and Krapp, CJ and Nadeau, JH and Willard, HF and Bartolomei, MS, An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse., Genetics, vol. 164 (August, 2003), pp. 1481--1494, ISSN 0016-6731 [12930754]  [abs]
  94. HF Willard, Tales of the Y chromosome., Nature, vol. 423 no. 6942 (June, 2003), pp. 810-1, 813, ISSN 0028-0836 [doi]
  95. Willard, HF, Tales of the Y chromosome., Nature, vol. 423 (June, 2003), pp. 810--813, ISSN 0028-0836 [12815408], [doi]
  96. BP Chadwick, HF Willard, SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome., Developmental cell, United States, vol. 4 no. 4 (April, 2003), pp. 445-7, ISSN 1534-5807  [abs]
  97. RS Williams, HF Willard, R Snyderman, Personalized health planning., Science (New York, N.Y.), United States, vol. 300 no. 5619 (April, 2003), pp. 549, ISSN 1095-9203 [doi]
  98. Chadwick, BP and Willard, HF, SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome., Dev Cell, vol. 4 (April, 2003), pp. 445--447, ISSN 1534-5807 [12689584]  [abs]
  99. Williams, RS and Willard, HF and Snyderman, R, Personalized health planning., Science, vol. 300 (April, 2003), pp. 549 [12714710], [doi]
  100. Rudd, MK and Schueler, MG and Willard, HF, Sequence organization and functional annotation of human centromeres., Cold Spring Harb Symp Quant Biol, vol. 68 (2003), pp. 141--149, ISSN 0091-7451 [15338612]
  101. Davies, K and Willard, H, Editorial, Human Molecular Genetics, vol. 12 (2003), pp. 699- [doi]
  102. Simpson, JL and Cruz, FDL and Swerdloff, RS and Samango-Sprouse, C and Skakkebaek, NE and Jr, JMG and Hassold, T and Aylstock, M and Meyer-Bahlburg, HFL and Willard, HF and Hall, JG and Salameh, W and Boone, K and Staessen, C and Geschwind, D and Giedd, J and Dobs, AS and Rogol, A and Brinton, B and Paulsen, CA, Klinefelter syndrome: Expanding the phenotype and identifying new research directions, Genetics in Medicine, vol. 5 (2003), pp. 460--468 [doi]  [abs]
  103. MK Rudd, MG Schueler, HF Willard, Sequence organization and functional annotation of human centromeres., Cold Spring Harbor symposia on quantitative biology, vol. 68 (2003), pp. 141-9, ISSN 0091-7451
  104. RM Plenge, RA Stevenson, HA Lubs, CE Schwartz, HF Willard, Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders., American journal of human genetics, United States, vol. 71 no. 1 (July, 2002), pp. 168-73, ISSN 0002-9297 [doi]  [abs]
  105. Plenge, RM and Stevenson, RA and Lubs, HA and Schwartz, CE and Willard, HF, Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders., Am J Hum Genet, vol. 71 (July, 2002), pp. 168--173, ISSN 0002-9297 [12068376], [doi]  [abs]
  106. BP Chadwick, HF Willard, Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome., The Journal of cell biology, vol. 157 no. 7 (June, 2002), pp. 1113-23, ISSN 0021-9525 [doi]  [abs]
  107. BR Grimes, AA Rhoades, HF Willard, Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation., Molecular therapy : the journal of the American Society of Gene Therapy, vol. 5 no. 6 (June, 2002), pp. 798-805, ISSN 1525-0016 [doi]  [abs]
  108. LL Hall, M Byron, K Sakai, L Carrel, HF Willard, JB Lawrence, An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 99 no. 13 (June, 2002), pp. 8677-82, ISSN 0027-8424 [doi]  [abs]
  109. Chadwick, BP and Willard, HF, Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome., J Cell Biol, vol. 157 (June, 2002), pp. 1113--1123, ISSN 0021-9525 [12082075], [doi]  [abs]
  110. Grimes, BR and Rhoades, AA and Willard, HF, Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation., Mol Ther, vol. 5 (June, 2002), pp. 798--805, ISSN 1525-0016 [12027565], [doi]  [abs]
  111. Hall, LL and Byron, M and Sakai, K and Carrel, L and Willard, HF and Lawrence, JB, An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells., Proc Natl Acad Sci U S A, vol. 99 (June, 2002), pp. 8677--8682, ISSN 0027-8424 [12072569], [doi]  [abs]
  112. I Percec, RM Plenge, JH Nadeau, MS Bartolomei, HF Willard, Autosomal dominant mutations affecting X inactivation choice in the mouse., Science (New York, N.Y.), vol. 296 no. 5570 (May, 2002), pp. 1136-9, ISSN 1095-9203 [doi]  [abs]
  113. Percec, I and Plenge, RM and Nadeau, JH and Bartolomei, MS and Willard, HF, Autosomal dominant mutations affecting X inactivation choice in the mouse., Science, vol. 296 (May, 2002), pp. 1136--1139 [12004136], [doi]  [abs]
  114. HF Willard, 2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics., American journal of human genetics, United States, vol. 70 no. 2 (February, 2002), pp. 285-96, ISSN 0002-9297
  115. Willard, HF, 2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics., Am J Hum Genet, vol. 70 (February, 2002), pp. 285--296, ISSN 0002-9297 [11781874]
  116. HF Willard, You say tomato and I say tomahto: human genetics and gene therapy., Molecular therapy : the journal of the American Society of Gene Therapy, United States, vol. 4 no. 6 (December, 2001), pp. 514, ISSN 1525-0016 [doi]
  117. Willard, HF, You say tomato and I say tomahto: human genetics and gene therapy., Mol Ther, vol. 4 (December, 2001), pp. 514, ISSN 1525-0016 [11735334], [doi]
  118. MG Schueler, AW Higgins, MK Rudd, K Gustashaw, HF Willard, Genomic and genetic definition of a functional human centromere., Science (New York, N.Y.), vol. 294 no. 5540 (October, 2001), pp. 109-15, ISSN 0036-8075 [doi]  [abs]
  119. Schueler, MG and Higgins, AW and Rudd, MK and Gustashaw, K and Willard, HF, Genomic and genetic definition of a functional human centromere., Science, vol. 294 (October, 2001), pp. 109--115, ISSN 0036-8075 [11588252], [doi]  [abs]
  120. HF Willard, L Carrel, Making sense (and antisense) of the X inactivation center., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 98 no. 18 (August, 2001), pp. 10025-7, ISSN 0027-8424 [doi]
  121. Willard, HF and Carrel, L, Making sense (and antisense) of the X inactivation center., Proc Natl Acad Sci U S A, vol. 98 (August, 2001), pp. 10025--10027, ISSN 0027-8424 [11526224], [doi]
  122. BP Chadwick, CM Valley, HF Willard, Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome., Nucleic acids research, England, vol. 29 no. 13 (July, 2001), pp. 2699-705, ISSN 1362-4962  [abs]
  123. Chadwick, BP and Valley, CM and Willard, HF, Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome., Nucleic Acids Res, vol. 29 (July, 2001), pp. 2699--2705 [11433014]  [abs]
  124. BP Chadwick, HF Willard, Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant., Human molecular genetics, England, vol. 10 no. 10 (May, 2001), pp. 1101-13, ISSN 0964-6906  [abs]
  125. HF Willard, Neocentromeres and human artificial chromosomes: an unnatural act., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 98 no. 10 (May, 2001), pp. 5374-6, ISSN 0027-8424 [doi]
  126. Willard, HF, Neocentromeres and human artificial chromosomes: an unnatural act., Proc Natl Acad Sci U S A, vol. 98 (May, 2001), pp. 5374--5376, ISSN 0027-8424 [11344277], [doi]
  127. Chadwick, BP and Willard, HF, Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant., Hum Mol Genet, vol. 10 (May, 2001), pp. 1101--1113, ISSN 0964-6906 [11331621]  [abs]
  128. JM Friedman, M Blitzer, LJ Elsas, U Francke, HF Willard, Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force., Genetics in medicine : official journal of the American College of Medical Genetics, United States, vol. 1 no. 1 , pp. 54-5, ISSN 1098-3600 [doi]
  129. BP Chadwick, HF Willard, A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome., The Journal of cell biology, United States, vol. 152 no. 2 (January, 2001), pp. 375-84, ISSN 0021-9525  [abs]
  130. Chadwick, BP and Willard, HF, A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome., J Cell Biol, vol. 152 (January, 2001), pp. 375--384, ISSN 0021-9525 [11266453]  [abs]
  131. Willard, HF, Evolution and function of alpha satellite DNA, Pathologie Biologie, vol. 49 (2001), pp. 390- [doi]
  132. HF Willard, Genomics and gene therapy. Artificial chromosomes coming to life., Science (New York, N.Y.), vol. 290 no. 5495 (November, 2000), pp. 1308-9, ISSN 0036-8075  [abs]
  133. Willard, HF, Genomics and gene therapy. Artificial chromosomes coming to life., Science, vol. 290 (November, 2000), pp. 1308--1309, ISSN 0036-8075 [11185406]  [abs]
  134. KD Tsuchiya, HF Willard, Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 11 no. 10 (October, 2000), pp. 849-54, ISSN 0938-8990  [abs]
  135. RM Plenge, I Percec, JH Nadeau, HF Willard, Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 11 no. 5 (May, 2000), pp. 405-8, ISSN 0938-8990
  136. MG Schueler, AW Higgins, R Nagaraja, D Tentler, N Dahl, K Gustashaw, HF Willard, Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation., Genomics, UNITED STATES, vol. 66 no. 1 (May, 2000), pp. 104-9, ISSN 0888-7543 [doi]  [abs]
  137. Schueler, MG and Higgins, AW and Nagaraja, R and Tentler, D and Dahl, N and Gustashaw, K and Willard, HF, Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation., Genomics, vol. 66 (May, 2000), pp. 104--109, ISSN 0888-7543 [10843811], [doi]  [abs]
  138. Plenge, RM and Percec, I and Nadeau, JH and Willard, HF, Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus., Mamm Genome, vol. 11 (May, 2000), pp. 405--408, ISSN 0938-8990 [10790543]
  139. M Thibonnier, MK Graves, MS Wagner, N Chatelain, F Soubrier, P Corvol, HF Willard, X Jeunemaitre, Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension., Journal of molecular and cellular cardiology, ENGLAND, vol. 32 no. 4 (April, 2000), pp. 557-64, ISSN 0022-2828 [doi]  [abs]
  140. Thibonnier, M and Graves, MK and Wagner, MS and Chatelain, N and Soubrier, F and Corvol, P and Willard, HF and Jeunemaitre, X, Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension., J Mol Cell Cardiol, vol. 32 (April, 2000), pp. 557--564, ISSN 0022-2828 [10756113], [doi]  [abs]
  141. Willard, HF, Artificial chromosomes coming to life, Science, vol. 290 (2000), pp. 1308--1309 [doi]
  142. L Carrel, AA Cottle, KC Goglin, HF Willard, A first-generation X-inactivation profile of the human X chromosome., Proceedings of the National Academy of Sciences of the United States of America, vol. 96 no. 25 (December, 1999), pp. 14440-4, ISSN 0027-8424  [abs]
  143. HF Willard, BD Hendrich, Breaking the silence in Rett syndrome., Nature genetics, UNITED STATES, vol. 23 no. 2 (October, 1999), pp. 127-8, ISSN 1061-4036 [doi]
  144. Willard, HF and Hendrich, BD, Breaking the silence in Rett syndrome., Nat Genet, vol. 23 (October, 1999), pp. 127--128, ISSN 1061-4036 [10508498], [doi]
  145. AW Higgins, MG Schueler, HF Willard, Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system., Chromosoma, GERMANY, vol. 108 no. 4 (August, 1999), pp. 256-65, ISSN 0009-5915  [abs]
  146. D Tentler, P Gustavsson, J Leisti, M Schueler, J Chelly, E Timonen, G Annerén, HF Willard, N Dahl, Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia., European journal of human genetics : EJHG, ENGLAND, vol. 7 no. 5 (July, 1999), pp. 541-8, ISSN 1018-4813 [doi]  [abs]
  147. Tentler, D and Gustavsson, P and Leisti, J and Schueler, M and Chelly, J and Timonen, E and Annerén, G and Willard, HF and Dahl, N, Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia., Eur J Hum Genet, vol. 7 (July, 1999), pp. 541--548, ISSN 1018-4813 [10439959], [doi]  [abs]
  148. L Carrel, HF Willard, Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others., Proceedings of the National Academy of Sciences of the United States of America, vol. 96 no. 13 (June, 1999), pp. 7364-9, ISSN 0027-8424  [abs]
  149. RM Plenge, L Tranebjaerg, PK Jensen, C Schwartz, HF Willard, Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation., American journal of human genetics, UNITED STATES, vol. 64 no. 3 (March, 1999), pp. 759-67, ISSN 0002-9297 [doi]  [abs]
  150. Plenge, RM and Tranebjaerg, L and Jensen, PK and Schwartz, C and Willard, HF, Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation., Am J Hum Genet, vol. 64 (March, 1999), pp. 759--767, ISSN 0002-9297 [10053010], [doi]  [abs]
  151. BA Sullivan, HF Willard, Stable dicentric X chromosomes with two functional centromeres., Nature genetics, UNITED STATES, vol. 20 no. 3 (November, 1998), pp. 227-8, ISSN 1061-4036 [doi]
  152. Sullivan, BA and Willard, HF, Stable dicentric X chromosomes with two functional centromeres., Nat Genet, vol. 20 (November, 1998), pp. 227--228, ISSN 1061-4036 [9806536], [doi]
  153. Friedman, JM and Blitzer, M and Elsas, LJ and Francke, U and Willard, HF, Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force., Genet Med, vol. 1 (November, 1998), pp. 54--55, ISSN 1098-3600 [11261431], [doi]
  154. L Carrel, HF Willard, Counting on Xist., Nature genetics, UNITED STATES, vol. 19 no. 3 (July, 1998), pp. 211-2, ISSN 1061-4036 [doi]
  155. AP Miller, HF Willard, Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 95 no. 15 (July, 1998), pp. 8709-14, ISSN 0027-8424  [abs]
  156. WM White, HF Willard, DL Van Dyke, DJ Wolff, The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA., American journal of human genetics, UNITED STATES, vol. 63 no. 1 (July, 1998), pp. 20-8, ISSN 0002-9297 [doi]  [abs]
  157. Miller, AP and Willard, HF, Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation., Proc Natl Acad Sci U S A, vol. 95 (July, 1998), pp. 8709--8714, ISSN 0027-8424 [9671743]  [abs]
  158. Carrel, L and Willard, HF, Counting on Xist., Nat Genet, vol. 19 (July, 1998), pp. 211--212, ISSN 1061-4036 [9662385], [doi]
  159. HF Willard, KE Davies, Genetics of disease Complex genetics, complex diseases, Curr Opin Genet Dev, vol. 8 no. 3 (June, 1998), pp. 271-3, ISSN 0959-437X
  160. T Haaf, HF Willard, Orangutan alpha-satellite monomers are closely related to the human consensus sequence., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 9 no. 6 (June, 1998), pp. 440-7, ISSN 0938-8990  [abs]
  161. Haaf, T and Willard, HF, Orangutan alpha-satellite monomers are closely related to the human consensus sequence., Mamm Genome, vol. 9 (June, 1998), pp. 440--447, ISSN 0938-8990 [9585431]  [abs]
  162. Willard, HF and Davies, KE, Genetics of disease Complex genetics, complex diseases, Curr Opin Genet Dev, vol. 8 (June, 1998), pp. 271--273 [9690994]
  163. HF Willard, Human artificial chromosomes coming into focus., Nature biotechnology, UNITED STATES, vol. 16 no. 5 (May, 1998), pp. 415-6, ISSN 1087-0156 [doi]
  164. Willard, HF, Human artificial chromosomes coming into focus., Nat Biotechnol, vol. 16 (May, 1998), pp. 415--416, ISSN 1087-0156 [9592384], [doi]
  165. HF Willard, Centromeres: the missing link in the development of human artificial chromosomes., Current opinion in genetics & development, ENGLAND, vol. 8 no. 2 (April, 1998), pp. 219-25, ISSN 0959-437X  [abs]
  166. A Greenfield, L Carrel, D Pennisi, C Philippe, N Quaderi, P Siggers, K Steiner, PP Tam, AP Monaco, HF Willard, P Koopman, The UTX gene escapes X inactivation in mice and humans., Human molecular genetics, ENGLAND, vol. 7 no. 4 (April, 1998), pp. 737-42, ISSN 0964-6906  [abs]
  167. Greenfield, A and Carrel, L and Pennisi, D and Philippe, C and Quaderi, N and Siggers, P and Steiner, K and Tam, PP and Monaco, AP and Willard, HF and Koopman, P, The UTX gene escapes X inactivation in mice and humans., Hum Mol Genet, vol. 7 (April, 1998), pp. 737--742, ISSN 0964-6906 [9499428]  [abs]
  168. Willard, HF, Centromeres: the missing link in the development of human artificial chromosomes., Curr Opin Genet Dev, vol. 8 (April, 1998), pp. 219--225, ISSN 0959-437X [9610413]  [abs]
  169. L Dal Zotto, NA Quaderi, R Elliott, PA Lingerfelter, L Carrel, V Valsecchi, E Montini, CH Yen, V Chapman, I Kalcheva, G Arrigo, O Zuffardi, S Thomas, HF Willard, A Ballabio, CM Disteche, EI Rugarli, The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region., Human molecular genetics, ENGLAND, vol. 7 no. 3 (March, 1998), pp. 489-99, ISSN 0964-6906  [abs]
  170. Dal Zotto, L and Quaderi, NA and Elliott, R and Lingerfelter, PA and Carrel, L and Valsecchi, V and Montini, E and Yen, CH and Chapman, V and Kalcheva, I and Arrigo, G and Zuffardi, O and Thomas, S and Willard, HF and Ballabio, A and Disteche, CM and Rugarli, EI, The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region., Hum Mol Genet, vol. 7 (March, 1998), pp. 489--499, ISSN 0964-6906 [9467009]  [abs]
  171. MM Mahtani, HF Willard, Physical and genetic mapping of the human X chromosome centromere: repression of recombination., Genome research, UNITED STATES, vol. 8 no. 2 (February, 1998), pp. 100-10, ISSN 1088-9051  [abs]
  172. Mahtani, MM and Willard, HF, Physical and genetic mapping of the human X chromosome centromere: repression of recombination., Genome Res, vol. 8 (February, 1998), pp. 100--110, ISSN 1088-9051 [9477338]  [abs]
  173. JM Puck, HF Willard, X inactivation in females with X-linked disease., The New England journal of medicine, UNITED STATES, vol. 338 no. 5 (January, 1998), pp. 325-8, ISSN 0028-4793 [doi]
  174. Puck, JM and Willard, HF, X inactivation in females with X-linked disease., N Engl J Med, vol. 338 (January, 1998), pp. 325--328, ISSN 0028-4793 [9445416], [doi]
  175. Willard, HF and Davies, KE, Complex genetics, complex diseases: Editorial overview, Current Opinion in Genetics and Development, vol. 8 (1998), pp. 271--273 [doi]
  176. RM Plenge, BD Hendrich, C Schwartz, JF Arena, A Naumova, C Sapienza, RM Winter, HF Willard, A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation., Nature genetics, UNITED STATES, vol. 17 no. 3 (November, 1997), pp. 353-6, ISSN 1061-4036 [doi]  [abs]
  177. RS James, P Dalton, K Gustashaw, DJ Wolff, HF Willard, C Mitchell, PA Jacobs, Molecular characterization of isochromosomes of Xq., Annals of human genetics, ENGLAND, vol. 61 no. Pt 6 (November, 1997), pp. 485-90, ISSN 0003-4800 [doi]  [abs]
  178. Plenge, RM and Hendrich, BD and Schwartz, C and Arena, JF and Naumova, A and Sapienza, C and Winter, RM and Willard, HF, A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation., Nat Genet, vol. 17 (November, 1997), pp. 353--356, ISSN 1061-4036 [9354806], [doi]  [abs]
  179. James, RS and Dalton, P and Gustashaw, K and Wolff, DJ and Willard, HF and Mitchell, C and Jacobs, PA, Molecular characterization of isochromosomes of Xq., Ann Hum Genet, vol. 61 (November, 1997), pp. 485--490, ISSN 0003-4800 [9543548], [doi]  [abs]
  180. T Haaf, HF Willard, Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4., Chromosoma, GERMANY, vol. 106 no. 4 (September, 1997), pp. 226-32, ISSN 0009-5915  [abs]
  181. Haaf, T and Willard, HF, Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4., Chromosoma, vol. 106 (September, 1997), pp. 226--232, ISSN 0009-5915 [9254724]  [abs]
  182. Y Ishikawa-Brush, JF Powell, P Bolton, AP Miller, F Francis, HF Willard, H Lehrach, AP Monaco, Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene., Human molecular genetics, ENGLAND, vol. 6 no. 8 (August, 1997), pp. 1241-50, ISSN 0964-6906  [abs]
  183. DJ Wolff, KM Gustashaw, V Zurcher, L Ko, W White, L Weiss, DL Van Dyke, S Schwartz, HF Willard, Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern., Human genetics, GERMANY, vol. 100 no. 2 (August, 1997), pp. 256-61, ISSN 0340-6717  [abs]
  184. TW Depinet, JL Zackowski, WC Earnshaw, S Kaffe, GS Sekhon, R Stallard, BA Sullivan, GH Vance, DL Van Dyke, HF Willard, AB Zinn, S Schwartz, Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA., Human molecular genetics, ENGLAND, vol. 6 no. 8 (August, 1997), pp. 1195-204, ISSN 0964-6906  [abs]
  185. Wolff, DJ and Gustashaw, KM and Zurcher, V and Ko, L and White, W and Weiss, L and Van Dyke, DL and Schwartz, S and Willard, HF, Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern., Hum Genet, vol. 100 (August, 1997), pp. 256--261, ISSN 0340-6717 [9254860]  [abs]
  186. Ishikawa-Brush, Y and Powell, JF and Bolton, P and Miller, AP and Francis, F and Willard, HF and Lehrach, H and Monaco, AP, Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene., Hum Mol Genet, vol. 6 (August, 1997), pp. 1241--1250, ISSN 0964-6906 [9259269]  [abs]
  187. Depinet, TW and Zackowski, JL and Earnshaw, WC and Kaffe, S and Sekhon, GS and Stallard, R and Sullivan, BA and Vance, GH and Van Dyke, DL and Willard, HF and Zinn, AB and Schwartz, S, Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA., Hum Mol Genet, vol. 6 (August, 1997), pp. 1195--1204, ISSN 0964-6906 [9259264]  [abs]
  188. BD Hendrich, RM Plenge, HF Willard, Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation., Nucleic acids research, ENGLAND, vol. 25 no. 13 (July, 1997), pp. 2661-71, ISSN 0305-1048  [abs]
  189. Hendrich, BD and Plenge, RM and Willard, HF, Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation., Nucleic Acids Res, vol. 25 (July, 1997), pp. 2661--2671, ISSN 0305-1048 [9185579]  [abs]
  190. CJ Brown, L Carrel, HF Willard, Expression of genes from the human active and inactive X chromosomes., American journal of human genetics, UNITED STATES, vol. 60 no. 6 (June, 1997), pp. 1333-43, ISSN 0002-9297 [doi]  [abs]
  191. Brown, CJ and Carrel, L and Willard, HF, Expression of genes from the human active and inactive X chromosomes., Am J Hum Genet, vol. 60 (June, 1997), pp. 1333--1343, ISSN 0002-9297 [9199554], [doi]  [abs]
  192. JJ Harrington, G Van Bokkelen, RW Mays, K Gustashaw, HF Willard, Formation of de novo centromeres and construction of first-generation human artificial microchromosomes., Nature genetics, UNITED STATES, vol. 15 no. 4 (April, 1997), pp. 345-55, ISSN 1061-4036 [doi]  [abs]
  193. Harrington, JJ and Van Bokkelen, G and Mays, RW and Gustashaw, K and Willard, HF, Formation of de novo centromeres and construction of first-generation human artificial microchromosomes., Nat Genet, vol. 15 (April, 1997), pp. 345--355, ISSN 1061-4036 [9090378], [doi]  [abs]
  194. HF Willard, HK Salz, Remodelling chromatin with RNA., Nature, ENGLAND, vol. 386 no. 6622 (March, 1997), pp. 228-9, ISSN 0028-0836 [doi]
  195. Willard, HF and Salz, HK, Remodelling chromatin with RNA., Nature, vol. 386 (March, 1997), pp. 228--229, ISSN 0028-0836 [9069277], [doi]
  196. James, RS and Dalton, P and Gustashaw, K and Wolff, DJ and Willard, HF and Mitchell, C and Jacobs, PA, Molecular characterization of isochromosomes of xq, Annals of Human Genetics, vol. 61 (1997), pp. 485--490, ISSN 0003-4800 [doi]  [abs]
  197. L Carrel, PA Hunt, HF Willard, Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene., Human molecular genetics, ENGLAND, vol. 5 no. 9 (September, 1996), pp. 1361-6, ISSN 0964-6906  [abs]
  198. Carrel, L and Hunt, PA and Willard, HF, Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene., Hum Mol Genet, vol. 5 (September, 1996), pp. 1361--1366, ISSN 0964-6906 [8872478]  [abs]
  199. HF Willard, Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 93 no. 14 (July, 1996), pp. 6847-50, ISSN 0027-8424
  200. HF Willard, X chromosome inactivation and X-linked mental retardation., American journal of medical genetics, UNITED STATES, vol. 64 no. 1 (July, 1996), pp. 21-6, ISSN 0148-7299 [doi]  [abs]
  201. L Carrel, HF Willard, An assay for X inactivation based on differential methylation at the fragile X locus, FMR1., American journal of medical genetics, UNITED STATES, vol. 64 no. 1 (July, 1996), pp. 27-30, ISSN 0148-7299 [doi]  [abs]
  202. HF Willard, X chromosome inactivation, XIST, and pursuit of the X-inactivation center., Cell, UNITED STATES, vol. 86 no. 1 (July, 1996), pp. 5-7, ISSN 0092-8674
  203. Willard, HF, Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function., Proc Natl Acad Sci U S A, vol. 93 (July, 1996), pp. 6847--6850, ISSN 0027-8424 [8692907]
  204. Willard, HF, X chromosome inactivation, XIST, and pursuit of the X-inactivation center., Cell, vol. 86 (July, 1996), pp. 5--7, ISSN 0092-8674 [8689687]
  205. Carrel, L and Willard, HF, An assay for X inactivation based on differential methylation at the fragile X locus, FMR1., Am J Med Genet, vol. 64 (July, 1996), pp. 27--30, ISSN 0148-7299 [8826444], [doi]  [abs]
  206. AK Naumova, RM Plenge, LM Bird, M Leppert, K Morgan, HF Willard, C Sapienza, Heritability of X chromosome--inactivation phenotype in a large family., American journal of human genetics, UNITED STATES, vol. 58 no. 6 (June, 1996), pp. 1111-9, ISSN 0002-9297  [abs]
  207. Naumova, AK and Plenge, RM and Bird, LM and Leppert, M and Morgan, K and Willard, HF and Sapienza, C, Heritability of X chromosome--inactivation phenotype in a large family., Am J Hum Genet, vol. 58 (June, 1996), pp. 1111--1119, ISSN 0002-9297 [8651287]  [abs]
  208. PE Warburton, T Haaf, J Gosden, D Lawson, HF Willard, Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes., Genomics, UNITED STATES, vol. 33 no. 2 (April, 1996), pp. 220-8, ISSN 0888-7543 [doi]  [abs]
  209. Warburton, PE and Haaf, T and Gosden, J and Lawson, D and Willard, HF, Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes., Genomics, vol. 33 (April, 1996), pp. 220--228, ISSN 0888-7543 [8660971], [doi]  [abs]
  210. L Carrel, CM Clemson, JM Dunn, AP Miller, PA Hunt, JB Lawrence, HF Willard, X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse., Human molecular genetics, ENGLAND, vol. 5 no. 3 (March, 1996), pp. 391-401, ISSN 0964-6906  [abs]
  211. Carrel, L and Clemson, CM and Dunn, JM and Miller, AP and Hunt, PA and Lawrence, JB and Willard, HF, X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse., Hum Mol Genet, vol. 5 (March, 1996), pp. 391--401, ISSN 0964-6906 [8852665]  [abs]
  212. CM Clemson, JA McNeil, HF Willard, JB Lawrence, XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure., The Journal of cell biology, UNITED STATES, vol. 132 no. 3 (February, 1996), pp. 259-75, ISSN 0021-9525  [abs]
  213. M Thibonnier, MK Graves, MS Wagner, C Auzan, E Clauser, HF Willard, Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene., Genomics, UNITED STATES, vol. 31 no. 3 (February, 1996), pp. 327-34, ISSN 0888-7543 [doi]  [abs]
  214. Clemson, CM and McNeil, JA and Willard, HF and Lawrence, JB, XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure., J Cell Biol, vol. 132 (February, 1996), pp. 259--275, ISSN 0021-9525 [8636206]  [abs]
  215. Thibonnier, M and Graves, MK and Wagner, MS and Auzan, C and Clauser, E and Willard, HF, Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene., Genomics, vol. 31 (February, 1996), pp. 327--334, ISSN 0888-7543 [8838314], [doi]  [abs]
  216. MP Coleman, HJ Ambrose, L Carrel, AH Németh, HF Willard, KE Davies, A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status., Genomics, UNITED STATES, vol. 31 no. 1 (January, 1996), pp. 135-8, ISSN 0888-7543 [doi]  [abs]
  217. DJ Wolff, AP Miller, DL Van Dyke, S Schwartz, HF Willard, Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation., American journal of human genetics, UNITED STATES, vol. 58 no. 1 (January, 1996), pp. 154-60, ISSN 0002-9297  [abs]
  218. Coleman, MP and Ambrose, HJ and Carrel, L and Németh, AH and Willard, HF and Davies, KE, A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status., Genomics, vol. 31 (January, 1996), pp. 135--138, ISSN 0888-7543 [8808293], [doi]  [abs]
  219. Wolff, DJ and Miller, AP and Van Dyke, DL and Schwartz, S and Willard, HF, Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation., Am J Hum Genet, vol. 58 (January, 1996), pp. 154--160, ISSN 0002-9297 [8554051]  [abs]
  220. Tranebjaerg, L and Lubs, HA and Borghgraef, M and Brown, WT and Fisch, G and J-, PF and Hagerman, R and Jacobs, PA and Mandel, JL and Mulley, J and Oostra, B and Schwartz, C and Sherman, S and Willard, H and Willems, P, Seventh International Workshop on the Fragile X and X-linked mental retardation, American Journal of Medical Genetics, vol. 64 (1996), pp. 1--14, ISSN 0148-7299 [doi]
  221. Sullivan, BA and Schwartz, S and Willard, HF, Centromeres of human chromosomes., Environ Mol Mutagen, vol. 28 (1996), pp. 182--191, ISSN 0893-6692 [8908179], [doi]  [abs]
  222. BA Sullivan, S Schwartz, HF Willard, Centromeres of human chromosomes., Environmental and molecular mutagenesis, UNITED STATES, vol. 28 no. 3 (1996), pp. 182-91, ISSN 0893-6692 [doi]  [abs]
  223. CU Kirchgessner, ST Warren, HF Willard, X inactivation of the FMR1 fragile X mental retardation gene., Journal of medical genetics, ENGLAND, vol. 32 no. 12 (December, 1995), pp. 925-9, ISSN 0022-2593  [abs]
  224. PE Warburton, HF Willard, Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages., Journal of molecular evolution, UNITED STATES, vol. 41 no. 6 (December, 1995), pp. 1006-15, ISSN 0022-2844  [abs]
  225. Kirchgessner, CU and Warren, ST and Willard, HF, X inactivation of the FMR1 fragile X mental retardation gene., J Med Genet, vol. 32 (December, 1995), pp. 925--929, ISSN 0022-2593 [8825916]  [abs]
  226. Warburton, PE and Willard, HF, Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages., J Mol Evol, vol. 41 (December, 1995), pp. 1006--1015, ISSN 0022-2844 [8587099]  [abs]
  227. R Sultana, DA Adler, S Edelhoff, L Carrel, KH Lee, VC Chapman, HF Willard, CM Disteche, The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation., Human molecular genetics, ENGLAND, vol. 4 no. 2 (February, 1995), pp. 257-63, ISSN 0964-6906  [abs]
  228. T Alitalo, F Francis, J Kere, H Lehrach, D Schlessinger, HF Willard, A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes., Genomics, UNITED STATES, vol. 25 no. 3 (February, 1995), pp. 691-700, ISSN 0888-7543  [abs]
  229. CJ Brown, AP Miller, L Carrel, JL Rupert, KE Davies, HF Willard, The DXS423E gene in Xp11.21 escapes X chromosome inactivation., Human molecular genetics, ENGLAND, vol. 4 no. 2 (February, 1995), pp. 251-5, ISSN 0964-6906  [abs]
  230. Sultana, R and Adler, DA and Edelhoff, S and Carrel, L and Lee, KH and Chapman, VC and Willard, HF and Disteche, CM, The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation., Hum Mol Genet, vol. 4 (February, 1995), pp. 257--263, ISSN 0964-6906 [7757076]  [abs]
  231. Brown, CJ and Miller, AP and Carrel, L and Rupert, JL and Davies, KE and Willard, HF, The DXS423E gene in Xp11.21 escapes X chromosome inactivation., Hum Mol Genet, vol. 4 (February, 1995), pp. 251--255, ISSN 0964-6906 [7757075]  [abs]
  232. Alitalo, T and Francis, F and Kere, J and Lehrach, H and Schlessinger, D and Willard, HF, A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes., Genomics, vol. 25 (February, 1995), pp. 691--700, ISSN 0888-7543 [7759104]  [abs]
  233. Davies, KE and Willard, HF, Editorial overview, Current Opinion in Genetics and Development, vol. 5 (1995), pp. 295--297 [doi]
  234. Rupert, JL and Brown, CJ and Willard, HF, Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene., Eur J Hum Genet, vol. 3 (1995), pp. 333--343, ISSN 1018-4813 [8825575]  [abs]
  235. Miller, AP and Gustashaw, K and Wolff, DJ and Rider, SH and Monaco, AP and Eble, B and Schlessinger, D and Gorski, JL and Ommen, GJV and Weissenbach, J and Willard, HF, Three genes that escape X chromosome inactivation are clustered within a 6 mb YAC contig and STS map in Xp11.21-p11.22, Human Molecular Genetics, vol. 4 (1995), pp. 731--739  [abs]
  236. Hendrich, BD and Willard, HF, Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals., Hum Mol Genet, vol. 4 Spec No (1995), pp. 1765--1777, ISSN 0964-6906 [8541877]  [abs]
  237. BD Hendrich, HF Willard, Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals., Human molecular genetics, ENGLAND, vol. 4 Spec No (1995), pp. 1765-77, ISSN 0964-6906  [abs]
  238. JL Rupert, CJ Brown, HF Willard, Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene., European journal of human genetics : EJHG, SWITZERLAND, vol. 3 no. 6 (1995), pp. 333-43, ISSN 1018-4813  [abs]
  239. KM Gustashaw, V Zurcher, LH Dickerman, R Stallard, HF Willard, Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation., American journal of medical genetics, UNITED STATES, vol. 53 no. 1 (October, 1994), pp. 39-45, ISSN 0148-7299 [doi]  [abs]
  240. Gustashaw, KM and Zurcher, V and Dickerman, LH and Stallard, R and Willard, HF, Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation., Am J Med Genet, vol. 53 (October, 1994), pp. 39--45, ISSN 0148-7299 [7802034], [doi]  [abs]
  241. RG Lafrenière, L Carrel, HF Willard, A novel transmembrane transporter encoded by the XPCT gene in Xq13.2., Human molecular genetics, ENGLAND, vol. 3 no. 7 (July, 1994), pp. 1133-9, ISSN 0964-6906  [abs]
  242. KA Rack, J Chelly, RJ Gibbons, S Rider, D Benjamin, RG Lafreniére, D Oscier, RW Hendriks, IW Craig, HF Willard, Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia., Human molecular genetics, ENGLAND, vol. 3 no. 7 (July, 1994), pp. 1053-9, ISSN 0964-6906  [abs]
  243. DJ Wolff, CJ Brown, S Schwartz, AM Duncan, U Surti, HF Willard, Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations., American journal of human genetics, UNITED STATES, vol. 55 no. 1 (July, 1994), pp. 87-95, ISSN 0002-9297  [abs]
  244. Wolff, DJ and Brown, CJ and Schwartz, S and Duncan, AM and Surti, U and Willard, HF, Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations., Am J Hum Genet, vol. 55 (July, 1994), pp. 87--95, ISSN 0002-9297 [8023855]  [abs]
  245. Rack, KA and Chelly, J and Gibbons, RJ and Rider, S and Benjamin, D and Lafreniére, RG and Oscier, D and Hendriks, RW and Craig, IW and Willard, HF, Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia., Hum Mol Genet, vol. 3 (July, 1994), pp. 1053--1059, ISSN 0964-6906 [7981672]  [abs]
  246. Lafrenière, RG and Carrel, L and Willard, HF, A novel transmembrane transporter encoded by the XPCT gene in Xq13.2., Hum Mol Genet, vol. 3 (July, 1994), pp. 1133--1139, ISSN 0964-6906 [7981683]  [abs]
  247. V Reed, SH Laval, V McCabe, HF Willard, Y Boyd, Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 5 no. 4 (April, 1994), pp. 237-40, ISSN 0938-8990
  248. Reed, V and Laval, SH and McCabe, V and Willard, HF and Boyd, Y, Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse., Mamm Genome, vol. 5 (April, 1994), pp. 237--240, ISSN 0938-8990 [8012115]
  249. CJ Brown, HF Willard, The human X-inactivation centre is not required for maintenance of X-chromosome inactivation., Nature, ENGLAND, vol. 368 no. 6467 (March, 1994), pp. 154-6, ISSN 0028-0836 [doi]  [abs]
  250. Brown, CJ and Willard, HF, The human X-inactivation centre is not required for maintenance of X-chromosome inactivation., Nature, vol. 368 (March, 1994), pp. 154--156, ISSN 0028-0836 [8139659], [doi]  [abs]
  251. Willard, HF and Cremers, F and Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D, Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994., Cytogenet Cell Genet, vol. 67 (1994), pp. 295--358, ISSN 0301-0171 [7924455]
  252. Willard, HF and Cremers, F and Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D, Report of the Fifth International Workshop on Human X Chromosome Mapping 1994, Cytogenetics and Cell Genetics, vol. 67 (1994), pp. 295--328
  253. Willard, HF and Davies, KE, Editorial, Human Molecular Genetics, vol. 3 (1994), pp. I+
  254. HF Willard, F Cremers, JL Mandel, AP Monaco, DL Nelson, D Schlessinger, Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994., Cytogenetics and cell genetics, SWITZERLAND, vol. 67 no. 4 (1994), pp. 295-358, ISSN 0301-0171
  255. AM Duncan, A Macdonald, CJ Brown, D Wolff, HF Willard, B Sutton, Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization., American journal of medical genetics, UNITED STATES, vol. 47 no. 8 (December, 1993), pp. 1153-6, ISSN 0148-7299 [doi]  [abs]
  256. Duncan, AM and Macdonald, A and Brown, CJ and Wolff, D and Willard, HF and Sutton, B, Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization., Am J Med Genet, vol. 47 (December, 1993), pp. 1153--1156, ISSN 0148-7299 [8291547], [doi]  [abs]
  257. GM Greig, PE Warburton, HF Willard, Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21., Journal of molecular evolution, UNITED STATES, vol. 37 no. 5 (November, 1993), pp. 464-75, ISSN 0022-2844  [abs]
  258. Greig, GM and Warburton, PE and Willard, HF, Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21., J Mol Evol, vol. 37 (November, 1993), pp. 464--475, ISSN 0022-2844 [8283478]  [abs]
  259. GM Greig, CB Sharp, L Carrel, HF Willard, Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies., Human molecular genetics, ENGLAND, vol. 2 no. 10 (October, 1993), pp. 1611-8, ISSN 0964-6906  [abs]
  260. PE Warburton, JS Waye, HF Willard, Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin., Molecular and cellular biology, UNITED STATES, vol. 13 no. 10 (October, 1993), pp. 6520-9, ISSN 0270-7306  [abs]
  261. HF Willard, The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain., Human molecular genetics, ENGLAND, vol. 2 no. 10 (October, 1993), pp. 1525-6, ISSN 0964-6906
  262. Willard, HF, The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain., Hum Mol Genet, vol. 2 (October, 1993), pp. 1525--1526, ISSN 0964-6906 [8268904]
  263. Greig, GM and Sharp, CB and Carrel, L and Willard, HF, Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies., Hum Mol Genet, vol. 2 (October, 1993), pp. 1611--1618, ISSN 0964-6906 [8268913]  [abs]
  264. Warburton, PE and Waye, JS and Willard, HF, Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin., Mol Cell Biol, vol. 13 (October, 1993), pp. 6520--6529, ISSN 0270-7306 [8413251]  [abs]
  265. RG Lafrenière, HF Willard, Pulsed-field map of Xq13 in the region of the human X inactivation center., Genomics, UNITED STATES, vol. 17 no. 2 (August, 1993), pp. 502-6, ISSN 0888-7543 [doi]  [abs]
  266. JM Puck, SM Deschênes, JC Porter, AS Dutra, CJ Brown, HF Willard, PS Henthorn, The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1., Human molecular genetics, ENGLAND, vol. 2 no. 8 (August, 1993), pp. 1099-104, ISSN 0964-6906  [abs]
  267. RG Lafrenière, CJ Brown, S Rider, J Chelly, P Taillon-Miller, AC Chinault, AP Monaco, HF Willard, 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes., Human molecular genetics, ENGLAND, vol. 2 no. 8 (August, 1993), pp. 1105-15, ISSN 0964-6906  [abs]
  268. Lafrenière, RG and Willard, HF, Pulsed-field map of Xq13 in the region of the human X inactivation center., Genomics, vol. 17 (August, 1993), pp. 502--506, ISSN 0888-7543 [8406503], [doi]  [abs]
  269. Lafrenière, RG and Brown, CJ and Rider, S and Chelly, J and Taillon-Miller, P and Chinault, AC and Monaco, AP and Willard, HF, 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes., Hum Mol Genet, vol. 2 (August, 1993), pp. 1105--1115, ISSN 0964-6906 [8401491]  [abs]
  270. Puck, JM and Deschênes, SM and Porter, JC and Dutra, AS and Brown, CJ and Willard, HF and Henthorn, PS, The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1., Hum Mol Genet, vol. 2 (August, 1993), pp. 1099--1104, ISSN 0964-6906 [8401490]  [abs]
  271. KA Leppig, CJ Brown, SL Bressler, K Gustashaw, RA Pagon, HF Willard, CM Disteche, Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST., Human molecular genetics, ENGLAND, vol. 2 no. 7 (July, 1993), pp. 883-7, ISSN 0964-6906  [abs]
  272. Leppig, KA and Brown, CJ and Bressler, SL and Gustashaw, K and Pagon, RA and Willard, HF and Disteche, CM, Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST., Hum Mol Genet, vol. 2 (July, 1993), pp. 883--887, ISSN 0964-6906 [8364571]  [abs]
  273. BD Hendrich, CJ Brown, HF Willard, Evolutionary conservation of possible functional domains of the human and murine XIST genes., Human molecular genetics, ENGLAND, vol. 2 no. 6 (June, 1993), pp. 663-72, ISSN 0964-6906  [abs]
  274. C Tyler-Smith, HF Willard, Mammalian chromosome structure., Current opinion in genetics & development, ENGLAND, vol. 3 no. 3 (June, 1993), pp. 390-7, ISSN 0959-437X  [abs]
  275. Tyler-Smith, C and Willard, HF, Mammalian chromosome structure., Curr Opin Genet Dev, vol. 3 (June, 1993), pp. 390--397, ISSN 0959-437X [8353411]  [abs]
  276. Hendrich, BD and Brown, CJ and Willard, HF, Evolutionary conservation of possible functional domains of the human and murine XIST genes., Hum Mol Genet, vol. 2 (June, 1993), pp. 663--672, ISSN 0964-6906 [8353487]  [abs]
  277. T Haaf, M Schmid, C Steinlein, PM Galetti, HF Willard, Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, ENGLAND, vol. 1 no. 1 (May, 1993), pp. 77-86, ISSN 0967-3849  [abs]
  278. HF Willard, The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene., Human molecular genetics, ENGLAND, vol. 2 no. 5 (May, 1993), pp. 497-8, ISSN 0964-6906
  279. Willard, HF, The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene., Hum Mol Genet, vol. 2 (May, 1993), pp. 497--498, ISSN 0964-6906 [8518785]
  280. Haaf, T and Schmid, M and Steinlein, C and Galetti, PM and Willard, HF, Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., Chromosome Res, vol. 1 (May, 1993), pp. 77--86, ISSN 0967-3849 [8143092]  [abs]
  281. MM Mahtani, HF Willard, A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci., Human molecular genetics, ENGLAND, vol. 2 no. 4 (April, 1993), pp. 431-7, ISSN 0964-6906  [abs]
  282. Mahtani, MM and Willard, HF, A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci., Hum Mol Genet, vol. 2 (April, 1993), pp. 431--437, ISSN 0964-6906 [8504304]  [abs]
  283. HF Willard, Cloning of the X-linked glycerol kinase gene., Human molecular genetics, ENGLAND, vol. 2 no. 2 (February, 1993), pp. 95-6, ISSN 0964-6906
  284. Willard, HF, Cloning of the X-linked glycerol kinase gene., Hum Mol Genet, vol. 2 (February, 1993), pp. 95--96, ISSN 0964-6906 [8499911]
  285. Brown, CJ and Willard, HF, Molecular and genetic studies of human X chromosome in activation, Advances in Developmental Biology (1992), vol. 2 (1993), pp. 37--72, ISSN 1566-3116
  286. Haaf, T and Schmid, M and Steinlein, C and Jr, PMG and Willard, HF, Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, vol. 1 (1993), pp. 77--86  [abs]
  287. Willard, HF and Brown, CJ and Carrel, L and Hendrich, B and Miller, AP, Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation., Cold Spring Harb Symp Quant Biol, vol. 58 (1993), pp. 315--322, ISSN 0091-7451 [7956044]
  288. Schlessinger, D and Mandel, JL and Monaco, AP and Nelson, DL and Willard, HF, Report of the Fourth International Workshop on Human X Chromosome mapping 1993, Cytogenetics and Cell Genetics, vol. 64 (1993), pp. 148--170
  289. Schlessinger, D and Mandel, JL and Monaco, AP and Nelson, DL and Willard, HF, Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993., Cytogenet Cell Genet, vol. 64 (1993), pp. 147--194, ISSN 0301-0171 [8404034]
  290. Willard, HF and Davies, KE, A sampler of current opinion, Current Opinion in Genetics and Development, vol. 3 (1993), pp. 387--389 [doi]
  291. HF Willard, CJ Brown, L Carrel, B Hendrich, AP Miller, Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation., Cold Spring Harbor symposia on quantitative biology, UNITED STATES, vol. 58 (1993), pp. 315-22, ISSN 0091-7451
  292. D Schlessinger, JL Mandel, AP Monaco, DL Nelson, HF Willard, Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993., Cytogenetics and cell genetics, SWITZERLAND, vol. 64 no. 3-4 (1993), pp. 147-94, ISSN 0301-0171
  293. R Wevrick, VP Willard, HF Willard, Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7., Genomics, UNITED STATES, vol. 14 no. 4 (December, 1992), pp. 912-23, ISSN 0888-7543  [abs]
  294. BJ Lorber, M Grantham, J Peters, HF Willard, TJ Hassold, Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin., American journal of human genetics, UNITED STATES, vol. 51 no. 6 (December, 1992), pp. 1265-76, ISSN 0002-9297  [abs]
  295. HF Willard, Centromeres--primary constrictions are primarily complicated., Human molecular genetics, ENGLAND, vol. 1 no. 9 (December, 1992), pp. 667-8, ISSN 0964-6906
  296. Lorber, BJ and Grantham, M and Peters, J and Willard, HF and Hassold, TJ, Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin., Am J Hum Genet, vol. 51 (December, 1992), pp. 1265--1276, ISSN 0002-9297 [1463010]  [abs]
  297. Willard, HF, Centromeres--primary constrictions are primarily complicated., Hum Mol Genet, vol. 1 (December, 1992), pp. 667--668, ISSN 0964-6906 [1302604]
  298. Wevrick, R and Willard, VP and Willard, HF, Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7., Genomics, vol. 14 (December, 1992), pp. 912--923, ISSN 0888-7543 [1478672]  [abs]
  299. PE Warburton, HF Willard, PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA., Nucleic acids research, ENGLAND, vol. 20 no. 22 (November, 1992), pp. 6033-42, ISSN 0305-1048  [abs]
  300. RA Bascom, J García-Heras, CL Hsieh, DS Gerhard, C Jones, U Francke, HF Willard, DH Ledbetter, RR McInnes, Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM., American journal of human genetics, UNITED STATES, vol. 51 no. 5 (November, 1992), pp. 1028-35, ISSN 0002-9297  [abs]
  301. Bascom, RA and García-Heras, J and Hsieh, CL and Gerhard, DS and Jones, C and Francke, U and Willard, HF and Ledbetter, DH and McInnes, RR, Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM., Am J Hum Genet, vol. 51 (November, 1992), pp. 1028--1035, ISSN 0002-9297 [1415249]  [abs]
  302. Warburton, PE and Willard, HF, PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA., Nucleic Acids Res, vol. 20 (November, 1992), pp. 6033--6042, ISSN 0305-1048 [1461735]  [abs]
  303. CJ Brown, BD Hendrich, JL Rupert, RG Lafrenière, Y Xing, J Lawrence, HF Willard, The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus., Cell, UNITED STATES, vol. 71 no. 3 (October, 1992), pp. 527-42, ISSN 0092-8674  [abs]
  304. JL Mandel, AP Monaco, DL Nelson, D Schlessinger, HF Willard, M Chipperfield, P Pearson, P Gilna, M Cinkosky, Genome maps III. 1992. Wall Chart., Science (New York, N.Y.), UNITED STATES, vol. 258 no. 5079 (October, 1992), pp. 87-102, ISSN 0036-8075
  305. Brown, CJ and Hendrich, BD and Rupert, JL and Lafrenière, RG and Xing, Y and Lawrence, J and Willard, HF, The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus., Cell, vol. 71 (October, 1992), pp. 527--542, ISSN 0092-8674 [1423611]  [abs]
  306. Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, HF and Chipperfield, M and Pearson, P and Gilna, P and Cinkosky, M, Genome maps III. 1992. Wall Chart., Science, vol. 258 (October, 1992), pp. 87--102, ISSN 0036-8075 [1439771]
  307. T Haaf, PE Warburton, HF Willard, Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation., Cell, UNITED STATES, vol. 70 no. 4 (August, 1992), pp. 681-96, ISSN 0092-8674  [abs]
  308. Haaf, T and Warburton, PE and Willard, HF, Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation., Cell, vol. 70 (August, 1992), pp. 681--696, ISSN 0092-8674 [1505032]  [abs]
  309. IA Corcos, RG Lafrenière, CR Begy, R Loch-Caruso, HF Willard, TW Glover, Refined localization of human connexin32 gene locus, GJB1, to Xq13.1., Genomics, UNITED STATES, vol. 13 no. 2 (June, 1992), pp. 479-80, ISSN 0888-7543  [abs]
  310. A Ballabio, HF Willard, Mammalian X-chromosome inactivation and the XIST gene., Current opinion in genetics & development, ENGLAND, vol. 2 no. 3 (June, 1992), pp. 439-47, ISSN 0959-437X  [abs]
  311. Corcos, IA and Lafrenière, RG and Begy, CR and Loch-Caruso, R and Willard, HF and Glover, TW, Refined localization of human connexin32 gene locus, GJB1, to Xq13.1., Genomics, vol. 13 (June, 1992), pp. 479--480, ISSN 0888-7543 [1319395]  [abs]
  312. Ballabio, A and Willard, HF, Mammalian X-chromosome inactivation and the XIST gene., Curr Opin Genet Dev, vol. 2 (June, 1992), pp. 439--447, ISSN 0959-437X [1504619]  [abs]
  313. T Haaf, HF Willard, Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2., Genomics, UNITED STATES, vol. 13 no. 1 (May, 1992), pp. 122-8, ISSN 0888-7543  [abs]
  314. PD Cotter, HF Willard, JL Gorski, DF Bishop, Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations., Genomics, UNITED STATES, vol. 13 no. 1 (May, 1992), pp. 211-2, ISSN 0888-7543  [abs]
  315. Cotter, PD and Willard, HF and Gorski, JL and Bishop, DF, Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations., Genomics, vol. 13 (May, 1992), pp. 211--212, ISSN 0888-7543 [1577484]  [abs]
  316. Haaf, T and Willard, HF, Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2., Genomics, vol. 13 (May, 1992), pp. 122--128, ISSN 0888-7543 [1577477]  [abs]
  317. CA Quigley, KJ Friedman, A Johnson, RG Lafreniere, LM Silverman, DB Lubahn, TR Brown, EM Wilson, HF Willard, FS French, Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status., The Journal of clinical endocrinology and metabolism, UNITED STATES, vol. 74 no. 4 (April, 1992), pp. 927-33, ISSN 0021-972X [doi]  [abs]
  318. Quigley, CA and Friedman, KJ and Johnson, A and Lafreniere, RG and Silverman, LM and Lubahn, DB and Brown, TR and Wilson, EM and Willard, HF and French, FS, Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status., J Clin Endocrinol Metab, vol. 74 (April, 1992), pp. 927--933, ISSN 0021-972X [1347772], [doi]  [abs]
  319. GM Greig, HF Willard, Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes., Genomics, UNITED STATES, vol. 12 no. 3 (March, 1992), pp. 573-80, ISSN 0888-7543  [abs]
  320. Greig, GM and Willard, HF, Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes., Genomics, vol. 12 (March, 1992), pp. 573--580, ISSN 0888-7543 [1559708]  [abs]
  321. Haaf, T and Sumner, AT and Köhler, J and Willard, HF and Schmid, M, A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma., Cytogenet Cell Genet, vol. 60 (1992), pp. 12--17, ISSN 0301-0171 [1582251]  [abs]
  322. Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, HF and Chipperfield, M and Pearson, P and Gilna, P and Cinkosky, M, Genome maps III, Science, vol. 258 (1992), pp. 87--88, ISSN 0036-8075
  323. Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, H, Genome analysis and the human X chromosome, Science, vol. 258 (1992), pp. 103--109, ISSN 0036-8075  [abs]
  324. Greig, GM and Willard, HF, β satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes, Genomics, vol. 12 (1992), pp. 573--580, ISSN 0888-7543  [abs]
  325. Dracopoli, NC and O'Connell, P and Elsner, TI and Lalouel, JM and White, RL and Buetow, KH and Nishimura, DY and Murray, JC and Helms, C and Mishra, SK and al, E, A comprehensive genetic linkage map of the human genome, Science, vol. 258 (1992), pp. 67--86  [abs]
  326. Haaf, T and Sumner, AT and Kohler, J and Willard, HF and Schmid, M, Erratum: A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma (Cytogenet Cell Genet 60:12-17 (1992)), Cytogenetics and Cell Genetics, vol. 61 (1992), pp. 224-
  327. Davies, KE and Willard, HF, Editorial, Human Molecular Genetics, vol. 1 (1992), pp. 3-, ISSN 0964-6906 [doi]
  328. T Haaf, AT Sumner, J Köhler, HF Willard, M Schmid, AT Summer, A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma., Cytogenetics and cell genetics, SWITZERLAND, vol. 60 no. 1 (1992), pp. 12-7, ISSN 0301-0171  [abs]
  329. MP Coleman, JC Murray, HF Willard, KF Nolan, KB Reid, DJ Blake, S Lindsay, SS Bhattacharya, A Wright, KE Davies, Genetic and physical mapping around the properdin P gene., Genomics, UNITED STATES, vol. 11 no. 4 (December, 1991), pp. 991-6, ISSN 0888-7543  [abs]
  330. HF Willard, Evolution of alpha satellite., Current opinion in genetics & development, ENGLAND, vol. 1 no. 4 (December, 1991), pp. 509-14, ISSN 0959-437X  [abs]
  331. Willard, HF, Evolution of alpha satellite., Curr Opin Genet Dev, vol. 1 (December, 1991), pp. 509--514, ISSN 0959-437X [1822282]  [abs]
  332. Coleman, MP and Murray, JC and Willard, HF and Nolan, KF and Reid, KB and Blake, DJ and Lindsay, S and Bhattacharya, SS and Wright, A and Davies, KE, Genetic and physical mapping around the properdin P gene., Genomics, vol. 11 (December, 1991), pp. 991--996, ISSN 0888-7543 [1783405]  [abs]
  333. PE Warburton, GM Greig, T Haaf, HF Willard, PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis., Genomics, UNITED STATES, vol. 11 no. 2 (October, 1991), pp. 324-33, ISSN 0888-7543  [abs]
  334. RG Lafrenière, CJ Brown, VE Powers, L Carrel, KE Davies, DF Barker, HF Willard, Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome., Genomics, UNITED STATES, vol. 11 no. 2 (October, 1991), pp. 352-63, ISSN 0888-7543  [abs]
  335. Lafrenière, RG and Brown, CJ and Powers, VE and Carrel, L and Davies, KE and Barker, DF and Willard, HF, Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome., Genomics, vol. 11 (October, 1991), pp. 352--363, ISSN 0888-7543 [1685139]  [abs]
  336. Warburton, PE and Greig, GM and Haaf, T and Willard, HF, PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis., Genomics, vol. 11 (October, 1991), pp. 324--333, ISSN 0888-7543 [1685138]  [abs]
  337. AP Losada, M Wessman, M Tiainen, AH Hopman, HF Willard, F Solé, MR Caballín, S Woessner, S Knuutila, Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study., Blood, UNITED STATES, vol. 78 no. 3 (August, 1991), pp. 775-9, ISSN 0006-4971  [abs]
  338. MM Mahtani, RG Lafrenière, TA Kruse, HF Willard, An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders., Genomics, UNITED STATES, vol. 10 no. 4 (August, 1991), pp. 849-57, ISSN 0888-7543  [abs]
  339. Losada, AP and Wessman, M and Tiainen, M and Hopman, AH and Willard, HF and Solé, F and Caballín, MR and Woessner, S and Knuutila, S, Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study., Blood, vol. 78 (August, 1991), pp. 775--779, ISSN 0006-4971 [1859890]  [abs]
  340. Mahtani, MM and Lafrenière, RG and Kruse, TA and Willard, HF, An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders., Genomics, vol. 10 (August, 1991), pp. 849--857, ISSN 0888-7543 [1916819]  [abs]
  341. CU Kirchgessner, JA Trofatter, MM Mahtani, HF Willard, LJ DeGennaro, A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes., American journal of human genetics, UNITED STATES, vol. 49 no. 1 (July, 1991), pp. 184-91, ISSN 0002-9297  [abs]
  342. Kirchgessner, CU and Trofatter, JA and Mahtani, MM and Willard, HF and DeGennaro, LJ, A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes., Am J Hum Genet, vol. 49 (July, 1991), pp. 184--191, ISSN 0002-9297 [1905878]  [abs]
  343. J Fujii, A Zarain-Herzberg, HF Willard, M Tada, DH MacLennan, Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6., The Journal of biological chemistry, UNITED STATES, vol. 266 no. 18 (June, 1991), pp. 11669-75, ISSN 0021-9258  [abs]
  344. Fujii, J and Zarain-Herzberg, A and Willard, HF and Tada, M and MacLennan, DH, Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6., J Biol Chem, vol. 266 (June, 1991), pp. 11669--11675, ISSN 0021-9258 [1828805]  [abs]
  345. RG Lafreniere, MT Geraghty, D Valle, TB Shows, HF Willard, Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm., Genomics, UNITED STATES, vol. 10 no. 1 (May, 1991), pp. 276-9, ISSN 0888-7543  [abs]
  346. R Wevrick, HF Willard, Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays., Nucleic acids research, ENGLAND, vol. 19 no. 9 (May, 1991), pp. 2295-301, ISSN 0305-1048  [abs]
  347. Wevrick, R and Willard, HF, Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays., Nucleic Acids Res, vol. 19 (May, 1991), pp. 2295--2301, ISSN 0305-1048 [2041770]  [abs]
  348. M Trifiro, B Gottlieb, L Pinsky, M Kaufman, L Prior, DD Belsham, K Wrogemann, CJ Brown, HF Willard, J Trapman, The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene., Molecular and cellular endocrinology, NETHERLANDS, vol. 75 no. 1 (January, 1991), pp. 37-47, ISSN 0303-7207  [abs]
  349. CJ Brown, RG Lafreniere, VE Powers, G Sebastio, A Ballabio, AL Pettigrew, DH Ledbetter, E Levy, IW Craig, HF Willard, Localization of the X inactivation centre on the human X chromosome in Xq13., Nature, ENGLAND, vol. 349 no. 6304 (January, 1991), pp. 82-4, ISSN 0028-0836 [doi]  [abs]
  350. CJ Brown, A Ballabio, JL Rupert, RG Lafreniere, M Grompe, R Tonlorenzi, HF Willard, A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome., Nature, ENGLAND, vol. 349 no. 6304 (January, 1991), pp. 38-44, ISSN 0028-0836 [doi]  [abs]
  351. Trifiro, M and Gottlieb, B and Pinsky, L and Kaufman, M and Prior, L and Belsham, DD and Wrogemann, K and Brown, CJ and Willard, HF and Trapman, J, The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene., Mol Cell Endocrinol, vol. 75 (January, 1991), pp. 37--47, ISSN 0303-7207 [2050265]  [abs]
  352. Brown, CJ and Lafreniere, RG and Powers, VE and Sebastio, G and Ballabio, A and Pettigrew, AL and Ledbetter, DH and Levy, E and Craig, IW and Willard, HF, Localization of the X inactivation centre on the human X chromosome in Xq13., Nature, vol. 349 (January, 1991), pp. 82--84, ISSN 0028-0836 [1985270], [doi]  [abs]
  353. Brown, CJ and Ballabio, A and Rupert, JL and Lafreniere, RG and Grompe, M and Tonlorenzi, R and Willard, HF, A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome., Nature, vol. 349 (January, 1991), pp. 38--44, ISSN 0028-0836 [1985261], [doi]  [abs]
  354. Davies, KE and Mandel, JL and Monaco, AP and Nussbaum, RL and Willard, HF, Report of the committee on the genetic constitution of the X chromosome, Cytogenetics and Cell Genetics, vol. 58 (1991), pp. 853--966
  355. Taylor, RG and García-Heras, J and Sadler, SJ and Lafreniere, RG and Willard, HF and Ledbetter, DH and McInnes, RR, Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1., Cytogenet Cell Genet, vol. 56 (1991), pp. 178--181, ISSN 0301-0171 [2055114]  [abs]
  356. Greig, GM and Parikh, S and George, J and Powers, VE and Willard, HF, Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms., Cytogenet Cell Genet, vol. 56 (1991), pp. 144--148, ISSN 0301-0171 [1675980]  [abs]
  357. Borsani, G and Tonlorenzi, R and Simmler, MC and Dandolo, L and Arnaud, D and Capra, V and Grompe, M and Pizzuti, A and Muzny, D and Lawrence, C and Willard, HF and Avner, P and Ballabio, A, Characterization of a murine gene expressed from the inactive X chromosome, Nature, vol. 351 (1991), pp. 325--329 [doi]  [abs]
  358. Franco, B and Guioli, S and Pragliola, A and Incerti, B and Bardoni, B and Tonlorenzi, R and Carrozzo, R and Maestrini, E and Pieretti, M and Taillon-Miller, P and Brown, CJ and Willard, HF and Lawrence, C and Persico, MG and Camerino, G and Ballabio, A, A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules, Nature, vol. 353 (1991), pp. 529--536 [doi]  [abs]
  359. Dracopoli, NC and O'Connell, P and Elsner, TI and Lalouel, JM and White, RL and Buetow, KH and Nishimura, DY and Murray, JC and Helms, C and Mishra, SK and Donis-Keller, H and Hall, JM and Lee, MK and King, MC and Attwood, J and Morton, NE and Robson, EB and Mahtani, M and Willard, HF and Royle, NJ and Patel, I and Jeffreys, AJ and Verga, V and Jenkins, T and Weber, JL and Mitchell, AL and Bale, AE, The CEPH consortium linkage map of human chromosome 1, Genomics, vol. 9 (1991), pp. 686--700, ISSN 0888-7543  [abs]
  360. GM Greig, S Parikh, J George, VE Powers, HF Willard, Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms., Cytogenetics and cell genetics, SWITZERLAND, vol. 56 no. 3-4 (1991), pp. 144-8, ISSN 0301-0171  [abs]
  361. RG Taylor, J García-Heras, SJ Sadler, RG Lafreniere, HF Willard, DH Ledbetter, RR McInnes, Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1., Cytogenetics and cell genetics, SWITZERLAND, vol. 56 no. 3-4 (1991), pp. 178-81, ISSN 0301-0171  [abs]
  362. KG Ten Hagen, DM Gilbert, HF Willard, SN Cohen, Replication timing of DNA sequences associated with human centromeres and telomeres., Molecular and cellular biology, UNITED STATES, vol. 10 no. 12 (December, 1990), pp. 6348-55, ISSN 0270-7306  [abs]
  363. HF Willard, Centromeres of mammalian chromosomes., Trends in genetics : TIG, ENGLAND, vol. 6 no. 12 (December, 1990), pp. 410-6, ISSN 0168-9525  [abs]
  364. R Wevrick, WC Earnshaw, PN Howard-Peebles, HF Willard, Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement., Molecular and cellular biology, UNITED STATES, vol. 10 no. 12 (December, 1990), pp. 6374-80, ISSN 0270-7306  [abs]
  365. EM Fisher, P Beer-Romero, LG Brown, A Ridley, JA McNeil, JB Lawrence, HF Willard, FR Bieber, DC Page, Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome., Cell, UNITED STATES, vol. 63 no. 6 (December, 1990), pp. 1205-18, ISSN 0092-8674  [abs]
  366. K Chun, N Mackay, HF Willard, BH Robinson, Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex., European journal of biochemistry / FEBS, GERMANY, vol. 194 no. 2 (December, 1990), pp. 587-92, ISSN 0014-2956  [abs]
  367. SJ Durfy, HF Willard, Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite., Journal of molecular biology, ENGLAND, vol. 216 no. 3 (December, 1990), pp. 555-66, ISSN 0022-2836 [doi]  [abs]
  368. Ten Hagen, KG and Gilbert, DM and Willard, HF and Cohen, SN, Replication timing of DNA sequences associated with human centromeres and telomeres., Mol Cell Biol, vol. 10 (December, 1990), pp. 6348--6355, ISSN 0270-7306 [2247059]  [abs]
  369. Wevrick, R and Earnshaw, WC and Howard-Peebles, PN and Willard, HF, Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement., Mol Cell Biol, vol. 10 (December, 1990), pp. 6374--6380, ISSN 0270-7306 [2247061]  [abs]
  370. Chun, K and Mackay, N and Willard, HF and Robinson, BH, Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex., Eur J Biochem, vol. 194 (December, 1990), pp. 587--592, ISSN 0014-2956 [1702713]  [abs]
  371. Fisher, EM and Beer-Romero, P and Brown, LG and Ridley, A and McNeil, JA and Lawrence, JB and Willard, HF and Bieber, FR and Page, DC, Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome., Cell, vol. 63 (December, 1990), pp. 1205--1218, ISSN 0092-8674 [2124517]  [abs]
  372. Durfy, SJ and Willard, HF, Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite., J Mol Biol, vol. 216 (December, 1990), pp. 555--566, ISSN 0022-2836 [2258932], [doi]  [abs]
  373. Willard, HF, Centromeres of mammalian chromosomes., Trends Genet, vol. 6 (December, 1990), pp. 410--416, ISSN 0168-9525 [2087784]  [abs]
  374. PE Warburton, HF Willard, Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA., Journal of molecular biology, ENGLAND, vol. 216 no. 1 (November, 1990), pp. 3-16, ISSN 0022-2836  [abs]
  375. Warburton, PE and Willard, HF, Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA., J Mol Biol, vol. 216 (November, 1990), pp. 3--16, ISSN 0022-2836 [2122000]  [abs]
  376. VM Watt, HF Willard, The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis., Human genetics, GERMANY, vol. 85 no. 6 (October, 1990), pp. 651-4, ISSN 0340-6717  [abs]
  377. RA Norum, RG Lafreniere, LW O'Neal, TF Nikolai, JP Delaney, JC Sisson, H Sobol, GM Lenoir, BA Ponder, HF Willard, Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A., Genomics, UNITED STATES, vol. 8 no. 2 (October, 1990), pp. 313-7, ISSN 0888-7543  [abs]
  378. Watt, VM and Willard, HF, The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis., Hum Genet, vol. 85 (October, 1990), pp. 651--654, ISSN 0340-6717 [1977688]  [abs]
  379. Norum, RA and Lafreniere, RG and O'Neal, LW and Nikolai, TF and Delaney, JP and Sisson, JC and Sobol, H and Lenoir, GM and Ponder, BA and Willard, HF, Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A., Genomics, vol. 8 (October, 1990), pp. 313--317, ISSN 0888-7543 [1979053]  [abs]
  380. T Ozçelik, RG Lafreniere, BT Archer, PA Johnston, HF Willard, U Francke, TC Südhof, Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., American journal of human genetics, UNITED STATES, vol. 47 no. 3 (September, 1990), pp. 551-61, ISSN 0002-9297  [abs]
  381. Ozçelik, T and Lafreniere, RG and Archer, BT and Johnston, PA and Willard, HF and Francke, U and Südhof, TC, Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., Am J Hum Genet, vol. 47 (September, 1990), pp. 551--561, ISSN 0002-9297 [1975480]  [abs]
  382. MM Mahtani, HF Willard, Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate., Genomics, UNITED STATES, vol. 7 no. 4 (August, 1990), pp. 607-13, ISSN 0888-7543  [abs]
  383. CB Sharp, HM Bedford, HF Willard, Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity., Human genetics, GERMANY, WEST, vol. 85 no. 3 (August, 1990), pp. 330-6, ISSN 0340-6717  [abs]
  384. K Otsu, HF Willard, VK Khanna, F Zorzato, NM Green, DH MacLennan, Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum., The Journal of biological chemistry, UNITED STATES, vol. 265 no. 23 (August, 1990), pp. 13472-83, ISSN 0021-9258  [abs]
  385. Mahtani, MM and Willard, HF, Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate., Genomics, vol. 7 (August, 1990), pp. 607--613, ISSN 0888-7543 [1974881]  [abs]
  386. Otsu, K and Willard, HF and Khanna, VK and Zorzato, F and Green, NM and MacLennan, DH, Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum., J Biol Chem, vol. 265 (August, 1990), pp. 13472--13483, ISSN 0021-9258 [2380170]  [abs]
  387. CJ Brown, AM Flenniken, BR Williams, HF Willard, X chromosome inactivation of the human TIMP gene., Nucleic acids research, ENGLAND, vol. 18 no. 14 (July, 1990), pp. 4191-5, ISSN 0305-1048  [abs]
  388. Brown, CJ and Flenniken, AM and Williams, BR and Willard, HF, X chromosome inactivation of the human TIMP gene., Nucleic Acids Res, vol. 18 (July, 1990), pp. 4191--4195, ISSN 0305-1048 [2377460]  [abs]
  389. RG Lafreniere, HF Willard, A BstE II RFLP at the DXS153 locus., Nucleic acids research, ENGLAND, vol. 18 no. 12 (June, 1990), pp. 3673, ISSN 0305-1048
  390. RG Lafreniere, HF Willard, A Rsal RFLP at the DXS467 locus., Nucleic acids research, ENGLAND, vol. 18 no. 12 (June, 1990), pp. 3673, ISSN 0305-1048
  391. AE MacKenzie, RG Korneluk, F Zorzato, J Fujii, M Phillips, D Iles, B Wieringa, S Leblond, J Bailly, HF Willard, The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy., American journal of human genetics, UNITED STATES, vol. 46 no. 6 (June, 1990), pp. 1082-9, ISSN 0002-9297  [abs]
  392. Lafreniere, RG and Willard, HF, A Rsal RFLP at the DXS467 locus., Nucleic Acids Res, vol. 18 (June, 1990), pp. 3673, ISSN 0305-1048 [1972984]
  393. Lafreniere, RG and Willard, HF, A BstE II RFLP at the DXS153 locus., Nucleic Acids Res, vol. 18 (June, 1990), pp. 3673, ISSN 0305-1048 [1972983]
  394. MacKenzie, AE and Korneluk, RG and Zorzato, F and Fujii, J and Phillips, M and Iles, D and Wieringa, B and Leblond, S and Bailly, J and Willard, HF, The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy., Am J Hum Genet, vol. 46 (June, 1990), pp. 1082--1089, ISSN 0002-9297 [1971150]  [abs]
  395. JT Clarke, HF Willard, I Teshima, PL Chang, MA Skomorowski, Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl., Clinical genetics, DENMARK, vol. 37 no. 5 (May, 1990), pp. 355-62, ISSN 0009-9163  [abs]
  396. Clarke, JT and Willard, HF and Teshima, I and Chang, PL and Skomorowski, MA, Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl., Clin Genet, vol. 37 (May, 1990), pp. 355--362, ISSN 0009-9163 [2112988]  [abs]
  397. JA Luty, Z Guo, HF Willard, DH Ledbetter, S Ledbetter, M Litt, Five polymorphic microsatellite VNTRs on the human X chromosome., American journal of human genetics, UNITED STATES, vol. 46 no. 4 (April, 1990), pp. 776-83, ISSN 0002-9297  [abs]
  398. J Fujii, HF Willard, DH MacLennan, Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene., Somatic cell and molecular genetics, UNITED STATES, vol. 16 no. 2 (March, 1990), pp. 185-9, ISSN 0740-7750  [abs]
  399. J Koch, S Kølvraa, N Hobolt, GB Petersen, HF Willard, JS Waye, N Gregersen, L Bolund, A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization., Clinical genetics, DENMARK, vol. 37 no. 3 (March, 1990), pp. 216-20, ISSN 0009-9163  [abs]
  400. Fujii, J and Willard, HF and MacLennan, DH, Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene., Somat Cell Mol Genet, vol. 16 (March, 1990), pp. 185--189, ISSN 0740-7750 [2321095]  [abs]
  401. Koch, J and Kølvraa, S and Hobolt, N and Petersen, GB and Willard, HF and Waye, JS and Gregersen, N and Bolund, L, A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization., Clin Genet, vol. 37 (March, 1990), pp. 216--220, ISSN 0009-9163 [2323091]  [abs]
  402. CJ Brown, HF Willard, Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation., American journal of human genetics, UNITED STATES, vol. 46 no. 2 (February, 1990), pp. 273-9, ISSN 0002-9297  [abs]
  403. Shier, P and Willard, HF and Watt, VM, Localization of the insulin receptor-related receptor gene to human chromosome 1., Cytogenet Cell Genet, vol. 54 (1990), pp. 80--81, ISSN 0301-0171 [2249481]  [abs]
  404. Willard, HF, Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction., Prog Clin Biol Res, vol. 360 (1990), pp. 39--52, ISSN 0361-7742 [2247510]
  405. Lafreniere, RG and Willard, HF, A RsaI RFLP at the DXS467 locus, Nucleic Acids Research, vol. 18 (1990), pp. 3673-, ISSN 0305-1048
  406. Davies, KE and Mandel, JL and Monaco, AP and Nussbaum, RL and Willard, HF, Report of the committee on the genetic constitution of the X chromosome., Cytogenet Cell Genet, vol. 55 (1990), pp. 254--313, ISSN 0301-0171 [2073838]
  407. KE Davies, JL Mandel, AP Monaco, RL Nussbaum, HF Willard, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 55 no. 1-4 (1990), pp. 254-313, ISSN 0301-0171
  408. HF Willard, Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction., Progress in clinical and biological research, UNITED STATES, vol. 360 (1990), pp. 39-52, ISSN 0361-7742
  409. P Shier, HF Willard, VM Watt, Localization of the insulin receptor-related receptor gene to human chromosome 1., Cytogenetics and cell genetics, SWITZERLAND, vol. 54 no. 1-2 (1990), pp. 80-1, ISSN 0301-0171  [abs]
  410. JN Dietz-Band, AE Turco, HF Willard, A Vincent, MH Skolnick, DF Barker, Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers., Cytogenetics and cell genetics, SWITZERLAND, vol. 54 no. 3-4 (1990), pp. 137-41, ISSN 0301-0171  [abs]
  411. R Wevrick, HF Willard, Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 86 no. 23 (December, 1989), pp. 9394-8, ISSN 0027-8424  [abs]
  412. GM Greig, SB England, HM Bedford, HF Willard, Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16., American journal of human genetics, UNITED STATES, vol. 45 no. 6 (December, 1989), pp. 862-72, ISSN 0002-9297  [abs]
  413. Wevrick, R and Willard, HF, Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability., Proc Natl Acad Sci U S A, vol. 86 (December, 1989), pp. 9394--9398, ISSN 0027-8424 [2594775]  [abs]
  414. Greig, GM and England, SB and Bedford, HM and Willard, HF, Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16., Am J Hum Genet, vol. 45 (December, 1989), pp. 862--872, ISSN 0002-9297 [2573999]  [abs]
  415. SJ Durfy, HF Willard, Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences., Genomics, UNITED STATES, vol. 5 no. 4 (November, 1989), pp. 810-21, ISSN 0888-7543  [abs]
  416. Durfy, SJ and Willard, HF, Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences., Genomics, vol. 5 (November, 1989), pp. 810--821, ISSN 0888-7543 [2591964]  [abs]
  417. WL Greer, MM Mahtani, PC Kwong, LA Rubin, M Peacocke, HF Willard, KA Siminovitch, Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction., Human genetics, GERMANY, WEST, vol. 83 no. 3 (October, 1989), pp. 227-30, ISSN 0340-6717  [abs]
  418. R Tran-Paterson, HF Willard, M Letarte, The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3., Cancer genetics and cytogenetics, UNITED STATES, vol. 42 no. 1 (October, 1989), pp. 129-34, ISSN 0165-4608  [abs]
  419. JS Waye, HF Willard, Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates., Chromosoma, GERMANY, WEST, vol. 98 no. 4 (October, 1989), pp. 273-9, ISSN 0009-5915  [abs]
  420. CJ Brown, HF Willard, Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect., American journal of human genetics, UNITED STATES, vol. 45 no. 4 (October, 1989), pp. 592-8, ISSN 0002-9297  [abs]
  421. Greer, WL and Mahtani, MM and Kwong, PC and Rubin, LA and Peacocke, M and Willard, HF and Siminovitch, KA, Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction., Hum Genet, vol. 83 (October, 1989), pp. 227--230, ISSN 0340-6717 [2571560]  [abs]
  422. Tran-Paterson, R and Willard, HF and Letarte, M, The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3., Cancer Genet Cytogenet, vol. 42 (October, 1989), pp. 129--134, ISSN 0165-4608 [2529024]  [abs]
  423. Waye, JS and Willard, HF, Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates., Chromosoma, vol. 98 (October, 1989), pp. 273--279, ISSN 0009-5915 [2515043]  [abs]
  424. Brown, CJ and Willard, HF, Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect., Am J Hum Genet, vol. 45 (October, 1989), pp. 592--598, ISSN 0002-9297 [2491017]  [abs]
  425. RG Lafreniere, MM Mahtani, HF Willard, An X-linked DraI RFLP recognized by cpX23 [DXS132], Nucleic acids research, ENGLAND, vol. 17 no. 16 (August, 1989), pp. 6754, ISSN 0305-1048
  426. JS Waye, HF Willard, Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 86 no. 16 (August, 1989), pp. 6250-4, ISSN 0027-8424  [abs]
  427. Lafreniere, RG and Mahtani, MM and Willard, HF, An X-linked DraI RFLP recognized by cpX23 [DXS132]., Nucleic Acids Res, vol. 17 (August, 1989), pp. 6754, ISSN 0305-1048 [2571121]
  428. Waye, JS and Willard, HF, Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA., Proc Natl Acad Sci U S A, vol. 86 (August, 1989), pp. 6250--6254, ISSN 0027-8424 [2762326]  [abs]
  429. JS Waye, HF Willard, Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3., Chromosoma, GERMANY, WEST, vol. 97 no. 6 (May, 1989), pp. 475-80, ISSN 0009-5915  [abs]
  430. Waye, JS and Willard, HF, Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3., Chromosoma, vol. 97 (May, 1989), pp. 475--480, ISSN 0009-5915 [2568244]  [abs]
  431. CJ Brown, VE Powers, DL Munroe, R Sheinin, HF Willard, Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation., Somatic cell and molecular genetics, UNITED STATES, vol. 15 no. 2 (March, 1989), pp. 173-8, ISSN 0740-7750  [abs]
  432. Brown, CJ and Powers, VE and Munroe, DL and Sheinin, R and Willard, HF, Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation., Somat Cell Mol Genet, vol. 15 (March, 1989), pp. 173--178, ISSN 0740-7750 [2928842]  [abs]
  433. HF Willard, SJ Durfy, MM Mahtani, H Dorkins, KE Davies, BR Williams, Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp., Human genetics, GERMANY, WEST, vol. 81 no. 3 (February, 1989), pp. 234-8, ISSN 0340-6717  [abs]
  434. C Logan, HF Willard, JM Rommens, AL Joyner, Chromosomal localization of the human homeo box-containing genes, EN1 and EN2., Genomics, UNITED STATES, vol. 4 no. 2 (February, 1989), pp. 206-9, ISSN 0888-7543  [abs]
  435. CJ Brown, SJ Goss, DB Lubahn, DR Joseph, EM Wilson, FS French, HF Willard, Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism., American journal of human genetics, UNITED STATES, vol. 44 no. 2 (February, 1989), pp. 264-9, ISSN 0002-9297  [abs]
  436. Logan, C and Willard, HF and Rommens, JM and Joyner, AL, Chromosomal localization of the human homeo box-containing genes, EN1 and EN2., Genomics, vol. 4 (February, 1989), pp. 206--209, ISSN 0888-7543 [2567700]  [abs]
  437. Brown, CJ and Goss, SJ and Lubahn, DB and Joseph, DR and Wilson, EM and French, FS and Willard, HF, Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism., Am J Hum Genet, vol. 44 (February, 1989), pp. 264--269, ISSN 0002-9297 [2563196]  [abs]
  438. Willard, HF and Durfy, SJ and Mahtani, MM and Dorkins, H and Davies, KE and Williams, BR, Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp., Hum Genet, vol. 81 (February, 1989), pp. 234--238, ISSN 0340-6717 [2921031]  [abs]
  439. CJ Brown, T Sekiguchi, T Nishimoto, HF Willard, Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13., Somatic cell and molecular genetics, UNITED STATES, vol. 15 no. 1 (January, 1989), pp. 93-6, ISSN 0740-7750  [abs]
  440. PR Fain, E Wright, HF Willard, K Stephens, DF Barker, The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints., American journal of human genetics, UNITED STATES, vol. 44 no. 1 (January, 1989), pp. 68-72, ISSN 0002-9297  [abs]
  441. K Stephens, P Green, VM Riccardi, S Ng, M Rising, D Barker, JK Darby, KM Falls, FS Collins, HF Willard, Genetic analysis of eight loci tightly linked to neurofibromatosis 1., American journal of human genetics, UNITED STATES, vol. 44 no. 1 (January, 1989), pp. 13-9, ISSN 0002-9297  [abs]
  442. Stephens, K and Green, P and Riccardi, VM and Ng, S and Rising, M and Barker, D and Darby, JK and Falls, KM and Collins, FS and Willard, HF, Genetic analysis of eight loci tightly linked to neurofibromatosis 1., Am J Hum Genet, vol. 44 (January, 1989), pp. 13--19, ISSN 0002-9297 [2491775]  [abs]
  443. Fain, PR and Wright, E and Willard, HF and Stephens, K and Barker, DF, The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints., Am J Hum Genet, vol. 44 (January, 1989), pp. 68--72, ISSN 0002-9297 [2491785]  [abs]
  444. Brown, CJ and Sekiguchi, T and Nishimoto, T and Willard, HF, Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13., Somat Cell Mol Genet, vol. 15 (January, 1989), pp. 93--96, ISSN 0740-7750 [2916166]  [abs]
  445. Robinson, BH and Chun, K and Mackay, N and Otulakowski, G and Petrova-Benedict, R and Willard, H, Isolated and combined deficiencies of the α-keto acid dehydrogenase complexes, Annals of the New York Academy of Sciences, vol. 573 (1989), pp. 337--346, ISSN 0077-8923 [doi]
  446. Alitalo, T and Willard, HF and de la Chapelle, A, Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7., Cytogenet Cell Genet, vol. 50 (1989), pp. 49--53, ISSN 0301-0171 [2743817]  [abs]
  447. Willard, HF and Wevrick, R and Warburton, PE, Human centromere structure: organization and potential role of alpha satellite DNA., Prog Clin Biol Res, vol. 318 (1989), pp. 9--18, ISSN 0361-7742 [2696978]
  448. Summar, ML and III, JAP and Krishnamani, MRS and Keefer, J and Trofatter, J and Schwartz, RC and Tsipouras, P and Willard, H and Ullrich, A, Protein kinase C: A new linkage marker for growth hormone and for COL1A1, Genomics, vol. 5 (1989), pp. 163--165, ISSN 0888-7543  [abs]
  449. Mandel, JL and Willard, HF and Nussbaum, RL and Romeo, G and Puck, JM and Davies, KE, Report of the committee on the genetic constitution of the X chromosome., Cytogenet Cell Genet, vol. 51 (1989), pp. 384--437, ISSN 0301-0171 [2676379]
  450. Kidd, KK and Bowcock, AM and Schmidtke, J and Track, RK and Ricciuti, F and Hutchings, G and Bale, A and Pearson, P and Willard, HF and Gelernter, J, Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms., Cytogenet Cell Genet, vol. 51 (1989), pp. 622--947, ISSN 0301-0171 [2676386]
  451. KK Kidd, AM Bowcock, J Schmidtke, RK Track, F Ricciuti, G Hutchings, A Bale, P Pearson, HF Willard, J Gelernter, Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms., Cytogenetics and cell genetics, SWITZERLAND, vol. 51 no. 1-4 (1989), pp. 622-947, ISSN 0301-0171
  452. HF Willard, R Wevrick, PE Warburton, Human centromere structure: organization and potential role of alpha satellite DNA., Progress in clinical and biological research, UNITED STATES, vol. 318 (1989), pp. 9-18, ISSN 0361-7742
  453. T Alitalo, HF Willard, A de la Chapelle, Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7., Cytogenetics and cell genetics, SWITZERLAND, vol. 50 no. 1 (1989), pp. 49-53, ISSN 0301-0171  [abs]
  454. HF Willard, The genomics of long tandem arrays of satellite DNA in the human genome., Genome / National Research Council Canada = Génome / Conseil national de recherches Canada, CANADA, vol. 31 no. 2 (1989), pp. 737-44, ISSN 0831-2796  [abs]
  455. JL Mandel, HF Willard, RL Nussbaum, G Romeo, JM Puck, KE Davies, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 51 no. 1-4 (1989), pp. 384-437, ISSN 0301-0171
  456. CJ Brown, MM Mahtani, HF Willard, Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome., Human genetics, GERMANY, WEST, vol. 80 no. 3 (November, 1988), pp. 296-8, ISSN 0340-6717  [abs]
  457. Brown, CJ and Mahtani, MM and Willard, HF, Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome., Hum Genet, vol. 80 (November, 1988), pp. 296--298, ISSN 0340-6717 [3192218]  [abs]
  458. P Devilee, RF Thierry, T Kievits, R Kolluri, AH Hopman, HF Willard, PL Pearson, CJ Cornelisse, Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes., Cancer research, UNITED STATES, vol. 48 no. 20 (October, 1988), pp. 5825-30, ISSN 0008-5472  [abs]
  459. GA Mitchell, JE Looney, LC Brody, G Steel, M Suchanek, JF Engelhardt, HF Willard, D Valle, Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene., The Journal of biological chemistry, UNITED STATES, vol. 263 no. 28 (October, 1988), pp. 14288-95, ISSN 0021-9258  [abs]
  460. Mitchell, GA and Looney, JE and Brody, LC and Steel, G and Suchanek, M and Engelhardt, JF and Willard, HF and Valle, D, Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene., J Biol Chem, vol. 263 (October, 1988), pp. 14288--14295, ISSN 0021-9258 [3170546]  [abs]
  461. Devilee, P and Thierry, RF and Kievits, T and Kolluri, R and Hopman, AH and Willard, HF and Pearson, PL and Cornelisse, CJ, Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes., Cancer Res, vol. 48 (October, 1988), pp. 5825--5830, ISSN 0008-5472 [3167839]  [abs]
  462. G Otulakowski, BH Robinson, HF Willard, Gene for lipoamide dehydrogenase maps to human chromosome 7., Somatic cell and molecular genetics, UNITED STATES, vol. 14 no. 4 (July, 1988), pp. 411-4, ISSN 0740-7750  [abs]
  463. P Devilee, T Kievits, JS Waye, PL Pearson, HF Willard, Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10., Genomics, UNITED STATES, vol. 3 no. 1 (July, 1988), pp. 1-7, ISSN 0888-7543  [abs]
  464. Devilee, P and Kievits, T and Waye, JS and Pearson, PL and Willard, HF, Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10., Genomics, vol. 3 (July, 1988), pp. 1--7, ISSN 0888-7543 [3220475]  [abs]
  465. Otulakowski, G and Robinson, BH and Willard, HF, Gene for lipoamide dehydrogenase maps to human chromosome 7., Somat Cell Mol Genet, vol. 14 (July, 1988), pp. 411--414, ISSN 0740-7750 [3399966]  [abs]
  466. MM Mahtani, HF Willard, A primary genetic map of the pericentromeric region of the human X chromosome., Genomics, UNITED STATES, vol. 2 no. 4 (May, 1988), pp. 294-301, ISSN 0888-7543  [abs]
  467. Mahtani, MM and Willard, HF, A primary genetic map of the pericentromeric region of the human X chromosome., Genomics, vol. 2 (May, 1988), pp. 294--301, ISSN 0888-7543 [2906040]  [abs]
  468. DB Lubahn, DR Joseph, PM Sullivan, HF Willard, FS French, EM Wilson, Cloning of human androgen receptor complementary DNA and localization to the X chromosome., Science (New York, N.Y.), UNITED STATES, vol. 240 no. 4850 (April, 1988), pp. 327-30, ISSN 0036-8075  [abs]
  469. Lubahn, DB and Joseph, DR and Sullivan, PM and Willard, HF and French, FS and Wilson, EM, Cloning of human androgen receptor complementary DNA and localization to the X chromosome., Science, vol. 240 (April, 1988), pp. 327--330, ISSN 0036-8075 [3353727]  [abs]
  470. R Allore, D O'Hanlon, R Price, K Neilson, HF Willard, DR Cox, A Marks, RJ Dunn, Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome., Science (New York, N.Y.), UNITED STATES, vol. 239 no. 4845 (March, 1988), pp. 1311-3, ISSN 0036-8075  [abs]
  471. JS Waye, RA Gravel, HF Willard, Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3., Nucleic acids research, ENGLAND, vol. 16 no. 5 (March, 1988), pp. 2362, ISSN 0305-1048
  472. Allore, R and O'Hanlon, D and Price, R and Neilson, K and Willard, HF and Cox, DR and Marks, A and Dunn, RJ, Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome., Science, vol. 239 (March, 1988), pp. 1311--1313, ISSN 0036-8075 [2964086]  [abs]
  473. Waye, JS and Gravel, RA and Willard, HF, Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3., Nucleic Acids Res, vol. 16 (March, 1988), pp. 2362, ISSN 0305-1048 [2895916]
  474. JE Spence, RG Perciaccante, GM Greig, HF Willard, DH Ledbetter, JF Hejtmancik, MS Pollack, WE O'Brien, AL Beaudet, Uniparental disomy as a mechanism for human genetic disease., American journal of human genetics, UNITED STATES, vol. 42 no. 2 (February, 1988), pp. 217-26, ISSN 0002-9297  [abs]
  475. Spence, JE and Perciaccante, RG and Greig, GM and Willard, HF and Ledbetter, DH and Hejtmancik, JF and Pollack, MS and O'Brien, WE and Beaudet, AL, Uniparental disomy as a mechanism for human genetic disease., Am J Hum Genet, vol. 42 (February, 1988), pp. 217--226, ISSN 0002-9297 [2893543]  [abs]
  476. JS Waye, AR Mitchell, HF Willard, Organization and genomic distribution of "82H" alpha satellite DNA. Evidence for a low-copy or single-copy alphoid domain located on human chromosome 14., Human genetics, GERMANY, WEST, vol. 78 no. 1 (January, 1988), pp. 27-32, ISSN 0340-6717  [abs]
  477. RG Worton, J Sutherland, JE Sylvester, HF Willard, S Bodrug, I Dubé, C Duff, V Kean, PN Ray, RD Schmickel, Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end., Science (New York, N.Y.), UNITED STATES, vol. 239 no. 4835 (January, 1988), pp. 64-8, ISSN 0036-8075  [abs]
  478. Worton, RG and Sutherland, J and Sylvester, JE and Willard, HF and Bodrug, S and Dubé, I and Duff, C and Kean, V and Ray, PN and Schmickel, RD, Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end., Science, vol. 239 (January, 1988), pp. 64--68, ISSN 0036-8075 [3336775]  [abs]
  479. Mandel, JL and Willard, HF and Nussbaum, RL and Davies, KE and Romeo, G, Report of the committee on the genetic constitution of the X chromosome., Cytogenet Cell Genet, vol. 49 (1988), pp. 107--128, ISSN 0301-0171 [2904879]
  480. MacLennan, DH and Brandi, CJ and Champaneria, S and Holland, PC and Powers, VE and Willard, HF, Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12, Somatic Cell and Molecular Genetics, vol. 14 (1988), pp. 645-, ISSN 0740-7750 [doi]
  481. Kidd, KK and Bowcock, AM and Pearson, PL and Schmidtke, J and Willard, HF and Track, RK and Ricciuti, F, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenet Cell Genet, vol. 49 (1988), pp. 132--218, ISSN 0301-0171 [2904880]
  482. Tsipouras, P and Schwartz, RC and Phillips, JA and Willard, HF, A centromere-based linkage group on the long arm of human chromosome 17., Cytogenet Cell Genet, vol. 47 (1988), pp. 109--110, ISSN 0301-0171 [3162714]  [abs]
  483. JL Mandel, HF Willard, RL Nussbaum, KE Davies, G Romeo, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 49 no. 1-3 (1988), pp. 107-28, ISSN 0301-0171
  484. KK Kidd, AM Bowcock, PL Pearson, J Schmidtke, HF Willard, RK Track, F Ricciuti, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 49 no. 1-3 (1988), pp. 132-218, ISSN 0301-0171
  485. P Tsipouras, RC Schwartz, JA Phillips, HF Willard, A centromere-based linkage group on the long arm of human chromosome 17., Cytogenetics and cell genetics, SWITZERLAND, vol. 47 no. 1-2 (1988), pp. 109-10, ISSN 0301-0171  [abs]
  486. HF Willard, GM Greig, VE Powers, JS Waye, Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis., Genomics, UNITED STATES, vol. 1 no. 4 (December, 1987), pp. 368-73, ISSN 0888-7543  [abs]
  487. CJ Brown, HF Willard, MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3., Nucleic acids research, ENGLAND, vol. 15 no. 22 (November, 1987), pp. 9614, ISSN 0305-1048
  488. Brown, CJ and Willard, HF, MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3., Nucleic Acids Res, vol. 15 (November, 1987), pp. 9614, ISSN 0305-1048 [2446265]
  489. JS Waye, GM Greig, HF Willard, Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11., Human genetics, GERMANY, WEST, vol. 77 no. 2 (October, 1987), pp. 151-6, ISSN 0340-6717  [abs]
  490. Waye, JS and Greig, GM and Willard, HF, Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11., Hum Genet, vol. 77 (October, 1987), pp. 151--156, ISSN 0340-6717 [2888719]  [abs]
  491. SJ Durfy, HF Willard, Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome., American journal of human genetics, UNITED STATES, vol. 41 no. 3 (September, 1987), pp. 391-401, ISSN 0002-9297  [abs]
  492. JS Waye, HF Willard, Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes., Nucleic acids research, ENGLAND, vol. 15 no. 18 (September, 1987), pp. 7549-69, ISSN 0305-1048  [abs]
  493. JS Waye, SJ Durfy, D Pinkel, S Kenwrick, M Patterson, KE Davies, HF Willard, Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA., Genomics, UNITED STATES, vol. 1 no. 1 (September, 1987), pp. 43-51, ISSN 0888-7543  [abs]
  494. B Vogelstein, ER Fearon, SR Hamilton, AC Preisinger, HF Willard, AM Michelson, AD Riggs, SH Orkin, Clonal analysis using recombinant DNA probes from the X-chromosome., Cancer research, UNITED STATES, vol. 47 no. 18 (September, 1987), pp. 4806-13, ISSN 0008-5472  [abs]
  495. Durfy, SJ and Willard, HF, Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome., Am J Hum Genet, vol. 41 (September, 1987), pp. 391--401, ISSN 0002-9297 [2888308]  [abs]
  496. Waye, JS and Willard, HF, Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes., Nucleic Acids Res, vol. 15 (September, 1987), pp. 7549--7569, ISSN 0305-1048 [3658703]  [abs]
  497. Waye, JS and Durfy, SJ and Pinkel, D and Kenwrick, S and Patterson, M and Davies, KE and Willard, HF, Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA., Genomics, vol. 1 (September, 1987), pp. 43--51, ISSN 0888-7543 [2889661]  [abs]
  498. Vogelstein, B and Fearon, ER and Hamilton, SR and Preisinger, AC and Willard, HF and Michelson, AM and Riggs, AD and Orkin, SH, Clonal analysis using recombinant DNA probes from the X-chromosome., Cancer Res, vol. 47 (September, 1987), pp. 4806--4813, ISSN 0008-5472 [2887283]  [abs]
  499. L Mengle-Gaw, HF Willard, CI Smith, L Hammarström, P Fischer, P Sherrington, G Lucas, PW Thompson, R Baer, TH Rabbitts, Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32., The EMBO journal, ENGLAND, vol. 6 no. 8 (August, 1987), pp. 2273-80, ISSN 0261-4189  [abs]
  500. Mengle-Gaw, L and Willard, HF and Smith, CI and Hammarström, L and Fischer, P and Sherrington, P and Lucas, G and Thompson, PW and Baer, R and Rabbitts, TH, Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32., EMBO J, vol. 6 (August, 1987), pp. 2273--2280, ISSN 0261-4189 [3117531]  [abs]
  501. DH MacLennan, CJ Brandl, S Champaneria, PC Holland, VE Powers, HF Willard, Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12., Somatic cell and molecular genetics, UNITED STATES, vol. 13 no. 4 (July, 1987), pp. 341-6, ISSN 0740-7750  [abs]
  502. MacLennan, DH and Brandl, CJ and Champaneria, S and Holland, PC and Powers, VE and Willard, HF, Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12., Somat Cell Mol Genet, vol. 13 (July, 1987), pp. 341--346, ISSN 0740-7750 [2842876]  [abs]
  503. BF O'Dowd, K Neote, DL Munroe, RA Gravel, D Mahuran, HF Willard, PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5., Nucleic acids research, ENGLAND, vol. 15 no. 7 (April, 1987), pp. 3194, ISSN 0305-1048
  504. O'Dowd, BF and Neote, K and Munroe, DL and Gravel, RA and Mahuran, D and Willard, HF, PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5., Nucleic Acids Res, vol. 15 (April, 1987), pp. 3194, ISSN 0305-1048 [2882486]
  505. DR Bell, JM Trent, HF Willard, JR Riordan, V Ling, Chromosomal location of human P-glycoprotein gene sequences., Cancer genetics and cytogenetics, UNITED STATES, vol. 25 no. 1 (March, 1987), pp. 141-8, ISSN 0165-4608  [abs]
  506. Bell, DR and Trent, JM and Willard, HF and Riordan, JR and Ling, V, Chromosomal location of human P-glycoprotein gene sequences., Cancer Genet Cytogenet, vol. 25 (March, 1987), pp. 141--148, ISSN 0165-4608 [2879621]  [abs]
  507. JS Wu, JR Riordan, HF Willard, R Milner, KK Kidd, MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone., Nucleic acids research, ENGLAND, vol. 15 no. 4 (February, 1987), pp. 1882, ISSN 0305-1048
  508. Wu, JS and Riordan, JR and Willard, HF and Milner, R and Kidd, KK, MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone., Nucleic Acids Res, vol. 15 (February, 1987), pp. 1882, ISSN 0305-1048 [2434933]
  509. JS Waye, SB England, HF Willard, Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome., Molecular and cellular biology, UNITED STATES, vol. 7 no. 1 (January, 1987), pp. 349-56, ISSN 0270-7306  [abs]
  510. Waye, JS and England, SB and Willard, HF, Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome., Mol Cell Biol, vol. 7 (January, 1987), pp. 349--356, ISSN 0270-7306 [3561394]  [abs]
  511. Barker, D and Wright, E and Nguyen, K and Cannon, L and Fain, P and Goldgar, D and Bishop, DT and Carey, J and Kivlin, J and Willard, H and Nakamura, Y and O'Connell, P and Leppert, M and White, R and Skolnick, M, A genomic search for linkage of neurofibromatosis to RFLPs, Journal of Medical Genetics, vol. 24 (1987), pp. 536--538  [abs]
  512. Barker, D and Green, P and Knowlton, R and Schumm, J and Lander, E and Oliphant, A and Willard, H and Akots, G and Brown, V and Gravius, T and Helms, C and Nelson, C and Parker, C and Rediker, K and Rising, M and Watt, D and Weiffenbach, B and Donis-Keller, H, Genetic linkage map of human chromosome 7 with 63 DNA markers, Proceedings of the National Academy of Sciences of the United States of America, vol. 84 (1987), pp. 8006--8010  [abs]
  513. Pearson, PL and Kidd, KK and Willard, HF, Human gene mapping by recombinant DNA techniques, Cytogenetics and Cell Genetics, vol. 46 (1987), pp. 390--566  [abs]
  514. Fain, PR and Barker, DF and Goldgar, DE and Wright, E and Nguyen, K and Carey, J and Johnson, J and Kivlin, J and Willard, H and Mathew, C and Ponder, B and Skolnick, M, Genetic analysis of NF1: Identification of close flanking markers on chromosome 17, Genomics, vol. 1 (1987), pp. 340--345, ISSN 0888-7543  [abs]
  515. Willard, HF and Waye, JS, Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat., J Mol Evol, vol. 25 (1987), pp. 207--214, ISSN 0022-2844 [2822935]  [abs]
  516. Willard, HF and Waye, JS, Hierarchical order in chromosome-specific human alpha satellite DNA, Trends in Genetics, vol. 3 (1987), pp. 192--198, ISSN 0168-9525  [abs]
  517. Pearson, PL and Kidd, KK and Willard, HF, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenet Cell Genet, vol. 46 (1987), pp. 390--566, ISSN 0301-0171 [3507285]
  518. Waye, JS and Creeper, LA and Willard, HF, Organization and evolution of alpha satellite DNA from human chromosome 11., Chromosoma, vol. 95 (1987), pp. 182--188, ISSN 0009-5915 [3608717]  [abs]
  519. HF Willard, JS Waye, Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat., Journal of molecular evolution, UNITED STATES, vol. 25 no. 3 (1987), pp. 207-14, ISSN 0022-2844  [abs]
  520. PL Pearson, KK Kidd, HF Willard, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 46 no. 1-4 (1987), pp. 390-566, ISSN 0301-0171
  521. JS Waye, LA Creeper, HF Willard, Organization and evolution of alpha satellite DNA from human chromosome 11., Chromosoma, GERMANY, WEST, vol. 95 no. 3 (1987), pp. 182-8, ISSN 0009-5915  [abs]
  522. SJ Durfy, SC Clark, BR Williams, HF Willard, RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)., Nucleic acids research, ENGLAND, vol. 14 no. 22 (November, 1986), pp. 9226, ISSN 0305-1048
  523. Durfy, SJ and Clark, SC and Williams, BR and Willard, HF, RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)., Nucleic Acids Res, vol. 14 (November, 1986), pp. 9226, ISSN 0305-1048 [2878423]
  524. BF O'Dowd, MH Klavins, HF Willard, R Gravel, JA Lowden, DJ Mahuran, Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)., The Journal of biological chemistry, UNITED STATES, vol. 261 no. 27 (September, 1986), pp. 12680-5, ISSN 0021-9258  [abs]
  525. JS Waye, HF Willard, Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation., Nucleic acids research, ENGLAND, vol. 14 no. 17 (September, 1986), pp. 6915-27, ISSN 0305-1048  [abs]
  526. JS Waye, HF Willard, Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome., Molecular and cellular biology, UNITED STATES, vol. 6 no. 9 (September, 1986), pp. 3156-65, ISSN 0270-7306  [abs]
  527. J Squire, TP Dryja, J Dunn, A Goddard, T Hofmann, M Musarella, HF Willard, AJ Becker, BL Gallie, RA Phillips, Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 17 (September, 1986), pp. 6573-7, ISSN 0027-8424  [abs]
  528. O'Dowd, BF and Klavins, MH and Willard, HF and Gravel, R and Lowden, JA and Mahuran, DJ, Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)., J Biol Chem, vol. 261 (September, 1986), pp. 12680--12685, ISSN 0021-9258 [3017984]  [abs]
  529. Waye, JS and Willard, HF, Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation., Nucleic Acids Res, vol. 14 (September, 1986), pp. 6915--6927, ISSN 0305-1048 [3763396]  [abs]
  530. Waye, JS and Willard, HF, Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome., Mol Cell Biol, vol. 6 (September, 1986), pp. 3156--3165, ISSN 0270-7306 [3785225]  [abs]
  531. Squire, J and Dryja, TP and Dunn, J and Goddard, A and Hofmann, T and Musarella, M and Willard, HF and Becker, AJ and Gallie, BL and Phillips, RA, Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13., Proc Natl Acad Sci U S A, vol. 83 (September, 1986), pp. 6573--6577, ISSN 0027-8424 [3462714]  [abs]
  532. HF Willard, JS Waye, MH Skolnick, CE Schwartz, VE Powers, SB England, Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 15 (August, 1986), pp. 5611-5, ISSN 0027-8424  [abs]
  533. Willard, HF and Waye, JS and Skolnick, MH and Schwartz, CE and Powers, VE and England, SB, Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps., Proc Natl Acad Sci U S A, vol. 83 (August, 1986), pp. 5611--5615, ISSN 0027-8424 [3016709]  [abs]
  534. T Glaser, WH Lewis, GA Bruns, PC Watkins, CE Rogler, TB Shows, VE Powers, HF Willard, JM Goguen, KO Simola, The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus., Nature, ENGLAND, vol. 321 no. 6073 , pp. 882-7, ISSN 0028-0836 [doi]  [abs]
  535. NE Cooke, HF Willard, EV David, DL George, Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism., Human genetics, GERMANY, WEST, vol. 73 no. 3 (July, 1986), pp. 225-9, ISSN 0340-6717  [abs]
  536. AM Lamhonwah, TJ Barankiewicz, HF Willard, DJ Mahuran, F Quan, RA Gravel, Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 13 (July, 1986), pp. 4864-8, ISSN 0027-8424  [abs]
  537. BR Williams, ME Saunders, HF Willard, Interferon-regulated human 2-5A synthetase gene maps to chromosome 12., Somatic cell and molecular genetics, UNITED STATES, vol. 12 no. 4 (July, 1986), pp. 403-8, ISSN 0740-7750  [abs]
  538. Williams, BR and Saunders, ME and Willard, HF, Interferon-regulated human 2-5A synthetase gene maps to chromosome 12., Somat Cell Mol Genet, vol. 12 (July, 1986), pp. 403--408, ISSN 0740-7750 [2426799]  [abs]
  539. Lamhonwah, AM and Barankiewicz, TJ and Willard, HF and Mahuran, DJ and Quan, F and Gravel, RA, Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes., Proc Natl Acad Sci U S A, vol. 83 (July, 1986), pp. 4864--4868, ISSN 0027-8424 [3460076]  [abs]
  540. Cooke, NE and Willard, HF and David, EV and George, DL, Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism., Hum Genet, vol. 73 (July, 1986), pp. 225--229, ISSN 0340-6717 [3015768]  [abs]
  541. RG Korneluk, DJ Mahuran, K Neote, MH Klavins, BF O'Dowd, M Tropak, HF Willard, MJ Anderson, JA Lowden, RA Gravel, Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease., The Journal of biological chemistry, UNITED STATES, vol. 261 no. 18 (June, 1986), pp. 8407-13, ISSN 0021-9258  [abs]
  542. Korneluk, RG and Mahuran, DJ and Neote, K and Klavins, MH and O'Dowd, BF and Tropak, M and Willard, HF and Anderson, MJ and Lowden, JA and Gravel, RA, Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease., J Biol Chem, vol. 261 (June, 1986), pp. 8407--8413, ISSN 0021-9258 [3013851]  [abs]
  543. Glaser, T and Lewis, WH and Bruns, GA and Watkins, PC and Rogler, CE and Shows, TB and Powers, VE and Willard, HF and Goguen, JM and Simola, KO, The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus., Nature, vol. 321 (June, 1986), pp. 882--887, ISSN 0028-0836 [3014343], [doi]  [abs]
  544. Buchwald, M and Zsiga, M and Markiewicz, D and Plavsic, N and Kennedy, D and Zengerling, S and Willard, HF and Tsipouras, P and Schmiegelow, K and Schwartz, M, Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7., Cytogenet Cell Genet, vol. 41 (1986), pp. 234--239, ISSN 0301-0171 [3011363]  [abs]
  545. Tsui, LC and Zengerling, S and Willard, HF and Buchwald, M, Mapping of the cystic fibrosis locus on chromosome 7., Cold Spring Harb Symp Quant Biol, vol. 51 Pt 1 (1986), pp. 325--335, ISSN 0091-7451 [3472729]
  546. Glaser, T and Lewis, WH and Bruns, GAP and Watkins, PC and Rogler, CE and Shows, TB and Powers, VE and Willard, HF and Goguen, JM and Simola, KO, The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus, Nature, vol. 321 (1986), pp. 882--887, ISSN 0028-0836 [doi]  [abs]
  547. LC Tsui, S Zengerling, HF Willard, M Buchwald, Mapping of the cystic fibrosis locus on chromosome 7., Cold Spring Harbor symposia on quantitative biology, UNITED STATES, vol. 51 Pt 1 (1986), pp. 325-35, ISSN 0091-7451
  548. M Buchwald, M Zsiga, D Markiewicz, N Plavsic, D Kennedy, S Zengerling, HF Willard, P Tsipouras, K Schmiegelow, M Schwartz, Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7., Cytogenetics and cell genetics, SWITZERLAND, vol. 41 no. 4 (1986), pp. 234-9, ISSN 0301-0171  [abs]
  549. HF Willard, JR Riordan, Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders., Science (New York, N.Y.), UNITED STATES, vol. 230 no. 4728 (November, 1985), pp. 940-2, ISSN 0036-8075  [abs]
  550. Willard, HF and Riordan, JR, Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders., Science, vol. 230 (November, 1985), pp. 940--942, ISSN 0036-8075 [3840606]  [abs]
  551. HF Willard, SO Meakin, LC Tsui, ML Breitman, Assignment of human gamma crystallin multigene family to chromosome 2., Somatic cell and molecular genetics, UNITED STATES, vol. 11 no. 5 (September, 1985), pp. 511-6, ISSN 0740-7750  [abs]
  552. Willard, HF and Meakin, SO and Tsui, LC and Breitman, ML, Assignment of human gamma crystallin multigene family to chromosome 2., Somat Cell Mol Genet, vol. 11 (September, 1985), pp. 511--516, ISSN 0740-7750 [2994242]  [abs]
  553. BJ Schmeckpeper, J Davis, HF Willard, KD Smith, An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]., Nucleic acids research, ENGLAND, vol. 13 no. 15 (August, 1985), pp. 5724, ISSN 0305-1048
  554. Schmeckpeper, BJ and Davis, J and Willard, HF and Smith, KD, An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]., Nucleic Acids Res, vol. 13 (August, 1985), pp. 5724, ISSN 0305-1048 [4041033]
  555. HF Willard, Chromosome-specific organization of human alpha satellite DNA., American journal of human genetics, UNITED STATES, vol. 37 no. 3 (May, 1985), pp. 524-32, ISSN 0002-9297  [abs]
  556. C Ingle, R Williamson, A de la Chapelle, RR Herva, K Haapala, G Bates, HF Willard, P Pearson, KE Davies, Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation., American journal of human genetics, UNITED STATES, vol. 37 no. 3 (May, 1985), pp. 451-62, ISSN 0002-9297  [abs]
  557. Willard, HF, Chromosome-specific organization of human alpha satellite DNA., Am J Hum Genet, vol. 37 (May, 1985), pp. 524--532, ISSN 0002-9297 [2988334]  [abs]
  558. Ingle, C and Williamson, R and de la Chapelle, A and Herva, RR and Haapala, K and Bates, G and Willard, HF and Pearson, P and Davies, KE, Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation., Am J Hum Genet, vol. 37 (May, 1985), pp. 451--462, ISSN 0002-9297 [2988331]  [abs]
  559. J Wolfe, SM Darling, RP Erickson, IW Craig, VJ Buckle, PW Rigby, HF Willard, PN Goodfellow, Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome., Journal of molecular biology, ENGLAND, vol. 182 no. 4 (April, 1985), pp. 477-85, ISSN 0022-2836  [abs]
  560. JS Waye, HF Willard, Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome., Nucleic acids research, ENGLAND, vol. 13 no. 8 (April, 1985), pp. 2731-43, ISSN 0305-1048  [abs]
  561. Waye, JS and Willard, HF, Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome., Nucleic Acids Res, vol. 13 (April, 1985), pp. 2731--2743, ISSN 0305-1048 [2987865]  [abs]
  562. Wolfe, J and Darling, SM and Erickson, RP and Craig, IW and Buckle, VJ and Rigby, PW and Willard, HF and Goodfellow, PN, Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome., J Mol Biol, vol. 182 (April, 1985), pp. 477--485, ISSN 0022-2836 [4040175]  [abs]
  563. E Bakker, MH Hofker, N Goor, JL Mandel, K Wrogemann, KE Davies, LM Kunkel, HF Willard, WA Fenton, L Sandkuyl, Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs., Lancet, ENGLAND, vol. 1 no. 8430 (March, 1985), pp. 655-8, ISSN 0140-6736  [abs]
  564. Bakker, E and Hofker, MH and Goor, N and Mandel, JL and Wrogemann, K and Davies, KE and Kunkel, LM and Willard, HF and Fenton, WA and Sandkuyl, L, Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs., Lancet, vol. 1 (March, 1985), pp. 655--658, ISSN 0140-6736 [2858615]  [abs]
  565. JS Rubin, VR Prideaux, HF Willard, AM Dulhanty, GF Whitmore, A Bernstein, Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene., Molecular and cellular biology, UNITED STATES, vol. 5 no. 2 (February, 1985), pp. 398-405, ISSN 0270-7306  [abs]
  566. BF O'Dowd, F Quan, HF Willard, AM Lamhonwah, RG Korneluk, JA Lowden, RA Gravel, DJ Mahuran, Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 82 no. 4 (February, 1985), pp. 1184-8, ISSN 0027-8424  [abs]
  567. Rubin, JS and Prideaux, VR and Willard, HF and Dulhanty, AM and Whitmore, GF and Bernstein, A, Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene., Mol Cell Biol, vol. 5 (February, 1985), pp. 398--405, ISSN 0270-7306 [2983193]  [abs]
  568. O'Dowd, BF and Quan, F and Willard, HF and Lamhonwah, AM and Korneluk, RG and Lowden, JA and Gravel, RA and Mahuran, DJ, Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase., Proc Natl Acad Sci U S A, vol. 82 (February, 1985), pp. 1184--1188, ISSN 0027-8424 [2579389]  [abs]
  569. Lewis, WH and Goguen, JM and Powers, VE and Willard, HF and Michalopoulos, EE, Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations., Hum Genet, vol. 71 (1985), pp. 249--253, ISSN 0340-6717 [3877676]  [abs]
  570. Willard, HF and Skolnick, MH and Pearson, PL and Mandel, JL, Report of the committee on human gene mapping by recombinant DNA techniques, Birth Defects: Original Article Series, vol. 21 (1985), pp. 360--489  [abs]
  571. Willard, HF and Goss, SJ and Holmes, MT and Munroe, DL, Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19., Hum Genet, vol. 71 (1985), pp. 138--143, ISSN 0340-6717 [2995234]  [abs]
  572. Willard, HF and Skolnick, MH and Pearson, PL and Mandel, JL, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenet Cell Genet, vol. 40 (1985), pp. 360--489, ISSN 0301-0171 [3864601]
  573. Saunders, M and Gewert, D and Castelino, M and Rutherford, M and Flenniken, A and Willard, H and Williams, BR, Characterization of the small 2-5A synthetase gene in human and mouse cells., Progress in clinical and biological research, vol. 202 (1985), pp. 163--174
  574. Michalopoulos, EE and Bevilacqua, PJ and Stokoe, N and Powers, VE and Willard, HF and Lewis, WH, Molecular analysis of gene deletion in aniridia--Wilms tumor association., Hum Genet, vol. 70 (1985), pp. 157--162, ISSN 0340-6717 [2989154]  [abs]
  575. EE Michalopoulos, PJ Bevilacqua, N Stokoe, VE Powers, HF Willard, WH Lewis, Molecular analysis of gene deletion in aniridia--Wilms tumor association., Human genetics, GERMANY, WEST, vol. 70 no. 2 (1985), pp. 157-62, ISSN 0340-6717  [abs]
  576. WH Lewis, JM Goguen, VE Powers, HF Willard, EE Michalopoulos, Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations., Human genetics, GERMANY, WEST, vol. 71 no. 3 (1985), pp. 249-53, ISSN 0340-6717  [abs]
  577. HF Willard, SJ Goss, MT Holmes, DL Munroe, Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19., Human genetics, GERMANY, WEST, vol. 71 no. 2 (1985), pp. 138-43, ISSN 0340-6717  [abs]
  578. HF Willard, MH Skolnick, PL Pearson, JL Mandel, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 40 no. 1-4 (1985), pp. 360-489, ISSN 0301-0171
  579. RG Korneluk, F Quan, WH Lewis, KS Guise, HF Willard, MT Holmes, RA Gravel, Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA., The Journal of biological chemistry, UNITED STATES, vol. 259 no. 22 (November, 1984), pp. 13819-23, ISSN 0021-9258  [abs]
  580. Korneluk, RG and Quan, F and Lewis, WH and Guise, KS and Willard, HF and Holmes, MT and Gravel, RA, Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA., J Biol Chem, vol. 259 (November, 1984), pp. 13819--13823, ISSN 0021-9258 [6548744]  [abs]
  581. RG Worton, C Duff, JE Sylvester, RD Schmickel, HF Willard, Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes., Science (New York, N.Y.), UNITED STATES, vol. 224 no. 4656 (June, 1984), pp. 1447-9, ISSN 0036-8075  [abs]
  582. Worton, RG and Duff, C and Sylvester, JE and Schmickel, RD and Willard, HF, Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes., Science, vol. 224 (June, 1984), pp. 1447--1449, ISSN 0036-8075 [6729462]  [abs]
  583. Caccia, N and Kronenberg, M and Saxe, D and Haars, R and Bruns, GAP and Goverman, J and Malissen, M and Willard, H and Yoshikai, Y and Simon, M and Hood, L and Mak, TW, The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans, Cell, vol. 37 (1984), pp. 1091--1099, ISSN 0092-8674  [abs]
  584. Willard, HF and Holmes, MT, A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids., Hum Genet, vol. 66 (1984), pp. 272--275, ISSN 0340-6717 [6585346]  [abs]
  585. Skolnick, MH and Willard, HF and Menlove, LA, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenet Cell Genet, vol. 37 (1984), pp. 210--273, ISSN 0301-0171 [6360559]
  586. MH Skolnick, HF Willard, LA Menlove, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 37 no. 1-4 (1984), pp. 210-73, ISSN 0301-0171
  587. HF Willard, MT Holmes, A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids., Human genetics, GERMANY, WEST, vol. 66 no. 2-3 (1984), pp. 272-5, ISSN 0340-6717  [abs]
  588. HF Willard, KD Smith, J Sutherland, Isolation and characterization of a major tandem repeat family from the human X chromosome., Nucleic acids research, ENGLAND, vol. 11 no. 7 (April, 1983), pp. 2017-33, ISSN 0305-1048  [abs]
  589. Willard, HF and Smith, KD and Sutherland, J, Isolation and characterization of a major tandem repeat family from the human X chromosome., Nucleic Acids Res, vol. 11 (April, 1983), pp. 2017--2033, ISSN 0305-1048 [6300789]  [abs]
  590. WA Fenton, AM Hack, HF Willard, A Gertler, LE Rosenberg, Purification and properties of methylmalonyl coenzyme A mutase from human liver., Archives of biochemistry and biophysics, UNITED STATES, vol. 214 no. 2 (April, 1982), pp. 815-23, ISSN 0003-9861
  591. Fenton, WA and Hack, AM and Willard, HF and Gertler, A and Rosenberg, LE, Purification and properties of methylmalonyl coenzyme A mutase from human liver., Arch Biochem Biophys, vol. 214 (April, 1982), pp. 815--823, ISSN 0003-9861 [6124211]
  592. BJ Schmeckpeper, HF Willard, KD Smith, Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome., Nucleic acids research, ENGLAND, vol. 9 no. 8 (April, 1981), pp. 1853-72, ISSN 0305-1048  [abs]
  593. Schmeckpeper, BJ and Willard, HF and Smith, KD, Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome., Nucleic Acids Res, vol. 9 (April, 1981), pp. 1853--1872, ISSN 0305-1048 [6264397]  [abs]
  594. HF Willard, WR Breg, Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes., Somatic cell genetics, UNITED STATES, vol. 6 no. 2 (March, 1980), pp. 187-98, ISSN 0098-0366  [abs]
  595. HF Willard, LE Rosenberg, Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites., Archives of biochemistry and biophysics, UNITED STATES, vol. 200 no. 1 (March, 1980), pp. 130-9, ISSN 0003-9861
  596. HF Willard, LE Rosenberg, Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression., The Journal of clinical investigation, UNITED STATES, vol. 65 no. 3 (March, 1980), pp. 690-8, ISSN 0021-9738 [doi]  [abs]
  597. Willard, HF and Rosenberg, LE, Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites., Arch Biochem Biophys, vol. 200 (March, 1980), pp. 130--139, ISSN 0003-9861 [6102452]
  598. Willard, HF and Rosenberg, LE, Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression., J Clin Invest, vol. 65 (March, 1980), pp. 690--698, ISSN 0021-9738 [6101601], [doi]  [abs]
  599. Willard, HF and Breg, WR, Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes., Somatic Cell Genet, vol. 6 (March, 1980), pp. 187--198, ISSN 0098-0366 [6156493]  [abs]
  600. B Wolf, HF Willard, LE Rosenberg, Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts., American journal of human genetics, UNITED STATES, vol. 32 no. 1 (January, 1980), pp. 16-25, ISSN 0002-9297  [abs]
  601. Wolf, B and Willard, HF and Rosenberg, LE, Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts., Am J Hum Genet, vol. 32 (January, 1980), pp. 16--25, ISSN 0002-9297 [7361761]  [abs]
  602. I Mellman, HF Willard, P Youngdahl-Turner, LE Rosenberg, Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells., The Journal of biological chemistry, UNITED STATES, vol. 254 no. 23 (December, 1979), pp. 11847-53, ISSN 0021-9258
  603. Mellman, I and Willard, HF and Youngdahl-Turner, P and Rosenberg, LE, Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells., J Biol Chem, vol. 254 (December, 1979), pp. 11847--11853, ISSN 0021-9258 [500677]
  604. HF Willard, LE Rosenberg, Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts., Biochemical genetics, UNITED STATES, vol. 17 no. 1-2 (February, 1979), pp. 57-75, ISSN 0006-2928  [abs]
  605. Willard, HF and Rosenberg, LE, Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts., Biochem Genet, vol. 17 (February, 1979), pp. 57--75, ISSN 0006-2928 [36882]  [abs]
  606. Willard, HF and Rosenberg, LE, Irreversible enzyme inhibition by hydroxocobalamin: Possible mechanism of water-soluble vitamin toxicity, Clinical Research, vol. 27 (1979), pp. 508A
  607. I Mellman, HF Willard, LE Rosenberg, Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts., The Journal of clinical investigation, UNITED STATES, vol. 62 no. 5 (November, 1978), pp. 952-60, ISSN 0021-9738 [doi]  [abs]
  608. Mellman, I and Willard, HF and Rosenberg, LE, Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts., J Clin Invest, vol. 62 (November, 1978), pp. 952--960, ISSN 0021-9738 [30783], [doi]  [abs]
  609. HF Willard, IS Mellman, LE Rosenberg, Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant., American journal of human genetics, UNITED STATES, vol. 30 no. 1 (January, 1978), pp. 1-13, ISSN 0002-9297
  610. Willard, HF and Mellman, IS and Rosenberg, LE, Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant., Am J Hum Genet, vol. 30 (January, 1978), pp. 1--13, ISSN 0002-9297 [23678]
  611. HF Willard, LE Rosenberg, Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin., Biochemical and biophysical research communications, UNITED STATES, vol. 78 no. 3 (October, 1977), pp. 927-34, ISSN 0006-291X
  612. Willard, HF and Rosenberg, LE, Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin., Biochem Biophys Res Commun, vol. 78 (October, 1977), pp. 927--934, ISSN 0006-291X [20894]
  613. HF Willard, Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes., Chromosoma, GERMANY, WEST, vol. 61 no. 1 (April, 1977), pp. 61-73, ISSN 0009-5915
  614. Willard, HF, Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes., Chromosoma, vol. 61 (April, 1977), pp. 61--73, ISSN 0009-5915 [69521]
  615. IS Mellman, P Youngdahl-Turner, HF Willard, LE Rosenberg, Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 74 no. 3 (March, 1977), pp. 916-20, ISSN 0027-8424  [abs]
  616. Willard, H and Mellman, I and Rosenberg, L, Biochemical heterogeneity within a class of human mutants deficient in cobalamin coenzyme synthesis International symposium on inborn errors of metabolism in man, Tel Aviv, June 19-25, 1977, Human Heredity, vol. 27 (1977), pp. 221-
  617. HF Willard, LM Ambani, AC Hart, MJ Mahoney, LE Rosenberg, Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells., Human genetics, GERMANY, WEST, vol. 34 no. 3 (December, 1976), pp. 277-83, ISSN 0340-6717  [abs]
  618. Willard, HF and Ambani, LM and Hart, AC and Mahoney, MJ and Rosenberg, LE, Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells., Hum Genet, vol. 34 (December, 1976), pp. 277--283, ISSN 0340-6717 [1002151]  [abs]
  619. SA Latt, HF Willard, PS Gerald, BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes., Chromosoma, GERMANY, WEST, vol. 57 no. 2 (August, 1976), pp. 135-53, ISSN 0009-5915  [abs]
  620. Latt, SA and Willard, HF and Gerald, PS, BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes., Chromosoma, vol. 57 (August, 1976), pp. 135--153, ISSN 0009-5915 [954550]  [abs]
  621. HF Willard, SA Latt, Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy., American journal of human genetics, UNITED STATES, vol. 28 no. 3 (May, 1976), pp. 213-27, ISSN 0002-9297  [abs]
  622. Willard, HF and Latt, SA, Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy., Am J Hum Genet, vol. 28 (May, 1976), pp. 213--227, ISSN 0002-9297 [1266850]  [abs]
  623. Willard, HF and Mahoney, MJ, Human X chromosomes: DNA replication sequence heterogeneity in different tissues, EXCERPTA MED.,AMSTERDAM,I.C.S., vol. No. 397 (1976), pp. No.444  [abs]
  624. Willard, HF and Ambani, LM and Mahoney, MJ and Rosenberg, LE, Detection and characterization of propionate methylmalonate disorders in cell culture: a simple method, Pediatric Research, vol. 10 (1976), pp. No.431
  625. SA Latt, G Stetten, LA Juergens, HF Willard, CD Scher, Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence., The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, UNITED STATES, vol. 23 no. 7 (July, 1975), pp. 493-505, ISSN 0022-1554  [abs]
  626. Latt, SA and Stetten, G and Juergens, LA and Willard, HF and Scher, CD, Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence., J Histochem Cytochem, vol. 23 (July, 1975), pp. 493--505, ISSN 0022-1554 [1095650]  [abs]
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