| Title | Author(s) | Year | View Count |
 | Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome | GarciaBarceló, M; So, MT; Lau, DKC; Leon, TYY; Yuan, ZW; Cai, WS; Lui, VCH; Fu, M; Herbrick, JA; Gutter, E; Proud, V; Li, L; PierreLouis, J; Aleck, K; Van Heurn, E; Belloni, E; Scherer, SW; Tam, PKH | 2006 | 177 |
| 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 | 680 |
| Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia | Ma, Z; Morris, SW; Valentine, V; L, M; Herbrick, JA; Cui, X; Bouman, D; Li, Y; Mehta, PK; Nizetic, D; Kaneko, Y; Chan, GCF; Chan, LC; Squire, J; Scherer, SW; Hitzler, JK | 2001 | 170 |
| Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24 | Crackower, MA; Sinasac, DS; Lee, JR; Herbrick, JA; Tsui, LC; Scherer, SW | 1999 | 124 |
 | Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy | Minassian, BA; Lee Jeffrey, R; Herbrick, JA; Huizenga, J; Soder, S; Mungall, AJ; Dunham, I; Gardner, R; Fong, CYG; Carpenter, S; Jardim, L; Satishchandra, P; Andermann, E; Carter Snead III, O; LopesCendes, I; Tsui, LC; DelgadoEscueta, AV; Rouleau, GA; Scherer, SW | 1998 | 630 |
| Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12 | Egan, S; Herbrick, JA; Tsui, LC; Cohen, B; Flock, G; Beatty, B; Scherer, SW | 1998 | 95 |
| Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre) | Coyle, B; Reardon, W; Herbrick, JA; Tsui, LC; Gausden, E; Lee, J; Coffey, R; Grueters, A; Grossman, A; Phelps, PD; Luxon, L; KendallTaylor, P; Scherer, SW; Trembath, RC | 1998 | 571 |
| PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7 | Osborne, LR; Herbrick, JA; Greavette, T; Heng, HHQ; Tsui, LC; Scherer, SW | 1997 | 213 |
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