people

Allison E Ashley-Koch

Associate Professor of Medicine
CCFP Faculty Fellow

Education:

• Ph.D. Emory University - 1997

Teaching Fall 2012:

• HGP 301B.16, RESEARCH IN HGP Synopsis
  TBA, 12:00 AM-11:59 PM
• HGP 301B.16-S, RESEARCH IN HGP Synopsis
  TBA, 12:00 AM-11:59 PM
• UPGEN 701.01, GENETICS & GENOMICS (ADV TOP) Synopsis
  TBA, W 06:15 PM-07:30 PM

Representative Publications   (More Publications)

1. P Sebastiani, N Solovieff, SW Hartley, JN Milton, A Riva, DA Dworkis, E Melista, ES Klings, ME Garrett, MJ Telen, A Ashley-Koch, CT Baldwin, MH Steinberg (2010). Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.. American journal of hematology, 85(1), 29-35. [doi]  [abs]


2. CA Markunas, KS Quinn, AL Collins, ME Garrett, AM Lachiewicz, JL Sommer, E Morrissey-Kane, SH Kollins, AD Anastopoulos, AE Ashley-Koch (2010). Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.. Psychiatric genetics, 20(2), 73-81. [doi]  [abs]


3. WD Taylor, DC Steffens, A Ashley-Koch, ME Payne, JR MacFall, CF Potocky, KR Krishnan (2010). Angiotensin receptor gene polymorphisms and 2-year change in hyperintense lesion volume in men.. Molecular psychiatry, 15(8), 816-22. [doi]  [abs]


4. SH Kollins, ME Garrett, FJ McClernon, AM Lachiewicz, E Morrissey-Kane, D FitzGerald, AL Collins, AD Anastopoulos, AE Ashley-Koch (2009). Effects of postnatal parental smoking on parent and teacher ratings of ADHD and oppositional symptoms.. The Journal of nervous and mental disease, 197(6), 442-9. [doi]  [abs]


5. S Züchner, JR Wendland, AE Ashley-Koch, AL Collins, KN Tran-Viet, K Quinn, KC Timpano, ML Cuccaro, MA Pericak-Vance, DC Steffens, KR Krishnan, G Feng, DL Murphy (2009). Multiple rare SAPAP3 missense variants in trichotillomania and OCD.. Molecular psychiatry, 14(1), 6-9. [doi]


6. KL Deak, DG Siegel, TM George, S Gregory, A Ashley-Koch, MC Speer, NTD Collaborative Group (2008). Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.. Birth defects research. Part A, Clinical and molecular teratology, 82(10), 662-9. [doi]  [abs]


7. S Zuchner, ML Cuccaro, KN Tran-Viet, H Cope, RR Krishnan, MA Pericak-Vance, HH Wright, A Ashley-Koch (2006). SLITRK1 mutations in trichotillomania.. Molecular psychiatry, England, 11(10), 887-9.


8. AE Ashley-Koch, H Mei, J Jaworski, DQ Ma, MD Ritchie, MM Menold, GR Delong, RK Abramson, HH Wright, JP Hussman, ML Cuccaro, JR Gilbert, ER Martin, MA Pericak-Vance (2006). An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.. Annals of human genetics, England, 70(Pt 3), 281-92.  [abs]


9. E Reid, M Kloos, A Ashley-Koch, L Hughes, S Bevan, IK Svenson, FL Graham, PC Gaskell, A Dearlove, MA Pericak-Vance, DC Rubinsztein, DA Marchuk (2002). A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).. American journal of human genetics, United States, 71(5), 1189-94.  [abs]


10. A Ashley-Koch, ER Bonner, PC Gaskell, SG West, R Tim, CM Wolpert, R Jones, CD Farrell, M Nance, IK Svenson, DA Marchuk, RM Boustany, JM Vance, WK Scott, MA Pericak-Vance (2001). Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.. Neurogenetics, England, 3(2), 91-7.  [abs]


11. A Ashley-Koch, CM Wolpert, MM Menold, L Zaeem, S Basu, SL Donnelly, SA Ravan, CM Powell, MB Qumsiyeh, AS Aylsworth, JM Vance, JR Gilbert, HH Wright, RK Abramson, GR DeLong, ML Cuccaro, MA Pericak-Vance (1999). Genetic studies of autistic disorder and chromosome 7.. Genomics, UNITED STATES, 61(3), 227-36.  [abs]


12. AE Ashley-Koch, H Robinson, AE Glicksman, SL Nolin, CE Schwartz, WT Brown, G Turner, SL Sherman (1998). Examination of factors associated with instability of the FMR1 CGG repeat.. American journal of human genetics, UNITED STATES, 63(3), 776-85.  [abs]