| Title | Author(s) | Year | View Count |  | Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C | Grafodatskaya, D; Chung, BHY; Butcher, DJ; Turinsky, AL; Goodman, SJ; Choufani, S; Chen, YA; Lou, Y; Zhao, C; Rajendram, R; Abidi, FE; Skinner, C; Stavropoulos, J; Bondy, CA; Hamilton, J; Wodak, S; Scherer, SW; Schwartz, CE; Weksberg, R | 2013 | 8 |
 | NSD1 mutations in Sotos syndrome alter the DNA methylation landscape of genes involved in somatic growth and neuronal transmission | Grafodatskaya, D; Inbar-Feigenberg, M; Chung, BHY; Cytrynbaum, C; Choufani, S | 2012 | 28 |
| Beckwith-Wiedemann Syndrome | Chung, BHY; Shuman, C; Choufani, S; Weksberg, R | 2012 | 63 |
| Beckwith-Wiedemann Syndrome | Chung, BHY; Shuman, C; Choufani, S; Weksberg, R | 2011 | 204 |
| Human chromosome 7: DNA sequence and biology | Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; ParkerKatiraee, L; Skaug, J; Khaja, R; Zhang, J; Hudek, AK; Li, M; Haddad, M; Duggan, GE; Fernandez, BA; Kanematsu, E; Gentles, S; Christopoulos, CC; Choufani, S; Kwasnicka, D; Zheng, XH; Lai, Z; Nusskern, D; Zhang, Q; Gu, Z; Lu, F; Zeesman, S; Nowaczyk, MJ; Teshima, I; Chitayat, D; Shuman, C; Weksberg, R; Zackai, EH; Grebe, TA; Cox, SR; Kirkpatrick, SJ; Rahman, N; Friedman, JM; Heng, HHQ; Pelicci, PG; LoCoco, F; Belloni, E; Shaffer, LG; Pober, B; Morton, CC; Gusella, JF; Bruns, GAP; Korf, BR; Quade, BJ; Ligon, AH; Ferguson, H; Higgins, AW; Leach, NT; Herrick, SR; Lemyre, E; Farra, CG; Kim, HG; Summers, AM; Gripp, KW; Roberts, W; Szatmari, P; Winsor, EJT; Grzeschik, KH; Teebi, A; Minassian, BA; Kere, J; Armengol, L; Pujana, MA; Estivill, X; Wilson, MD; Koop, BF; Tosi, S; Moore, GE; Boright, AP; Zlotorynski, E; Kerem, B; Kroisel, PM; Petek, E; Oscier, DG; Mould, SJ; Döhner, H; Döhner, K; Rommens, JM; Vincent, JB; Venter, JC; Li, PW; Mural, RJ; Adams, MD; Tsui, LC | 2003 | 694 |
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