David B. Goldstein, Professor of Molecular Genetics & Microbiology and Professor of Biology  

David B. Goldstein

Education:
Ph.D., Stanford University, 1994

Office Location: MGM--GSRB2
Office Phone: (919) 684-0896
Email Address: d.goldstein@duke.edu

Recent Publications   (More Publications)   (search)

  1. Sanna-Cherchi, S; Khan, K; Westland, R; Krithivasan, P; Fievet, L; Rasouly, HM; Ionita-Laza, I; Capone, VP; Fasel, DA; Kiryluk, K; Kamalakaran, S; Bodria, M; Otto, EA; Sampson, MG; Gillies, CE; Vega-Warner, V; Vukojevic, K; Pediaditakis, I; Makar, GS; Mitrotti, A; Verbitsky, M; Martino, J; Liu, Q; Na, YJ; Goj, V; Ardissino, G; Gigante, M; Gesualdo, L; Janezcko, M; Zaniew, M; Mendelsohn, CL; Shril, S; Hildebrandt, F; van Wijk, JAE; Arapovic, A; Saraga, M; Allegri, L; Izzi, C; Scolari, F et al., Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018)), The American Journal of Human Genetics, vol. 101 no. 6 (December, 2017), pp. 1034 [doi]  [abs].
  2. Sanders, SJ; Neale, BM; Huang, H; Werling, DM; An, JY; Dong, S; Abecasis, G; Arguello, PA; Blangero, J; Boehnke, M; Daly, MJ; Eggan, K; Geschwind, DH; Glahn, DC; Goldstein, DB; Gur, RE; Handsaker, RE; McCarroll, SA; Ophoff, RA; Palotie, A; Pato, CN; Sabatti, C; State, MW; Jeremy Willsey, A; Hyman, SE; Addington, AM; Lehner, T; Freimer, NB, Whole genome sequencing in psychiatric disorders: The WGSPD consortium, Nature Neuroscience, vol. 20 no. 12 (December, 2017), pp. 1661-1668 [doi]  [abs].
  3. Rotemberg, V; Garzon, M; Lauren, C; Iglesias, A; Brachio, SS; Aggarwal, V; Stong, N; Goldstein, DB; Diacovo, T, A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis Bullosa., The Journal of Pediatrics, vol. 191 (December, 2017), pp. 266-269.e1 [doi]  [abs].
  4. Revah-Politi, A; Ganapathi, M; Bier, L; Cho, MT; Goldstein, DB; Hemati, P; Iglesias, A; Juusola, J; Pappas, J; Petrovski, S; Wilson, AL; Aggarwal, VS; Anyane-Yeboa, K, Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series., American Journal of Medical Genetics Part A, vol. 173 no. 12 (December, 2017), pp. 3158-3164 [doi]  [abs].
  5. Zhu, X; Padmanabhan, R; Copeland, B; Bridgers, J; Ren, Z; Kamalakaran, S; O'Driscoll-Collins, A; Berkovic, SF; Scheffer, IE; Poduri, A; Mei, D; Guerrini, R; Lowenstein, DH; Allen, AS; Heinzen, EL; Goldstein, DB, A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations., PLoS genetics, vol. 13 no. 11 (November, 2017), pp. e1007104 [doi]  [abs].