| Title | Author(s) | Year | View Count |
 | Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia | Feuk, L; Kalervo, A; LipsanenNyman, M; Skaug, J; Nakabayashi, K; Finucane, B; Hartung, D; Innes, M; Kerem, B; Nowaczyk, MJ; Rivlin, J; Roberts, W; Senman, L; Summers, A; Szatmari, P; Wong, V; Vincent, JB; Zeesman, S; Osborne, LR; Cardy, JO; Kere, J; Scherer, SW; HannulaJouppi, K | 2006 | 462 |
 | 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 |
| Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients | Wu, YQ; Bejjani, BA; Tsui, LC; Mandel, A; Osborne, LR; Shaffer, LG | 2002 | 200 |
| A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome | Osborne, LR; Li, M; Pober, B; Chitayat, D; Bodurtha, J; Mandel, A; Costa, T; Grebe, T; Cox, S; Tsui, LC; Scherer, SW | 2001 | 1,747 |
| Influence of restraint stress on the expression and the serine/threonine phosphatase activity of calcineurin in the rat brain | Wu, YQ; Bejjani, BA; Tsui, LC; Mandel, A; Osborne, LR; Shaffer, LG | 2001 | 35 |
 | Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome | Osborne, LR; Campbell, T; Daradich, A; Scherer, SW; Tsui, LC | 1999 | 208 |
| Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23 | Nomiyama, H; Osborne, LR; Imai, T; Kusuda, J; Miura, R; Tsui, LC; Yoshie, O | 1998 | 109 |
| The BCL7 gene family: Deletion of BCL7B in Williams syndrome | Jadayel, DM; Osborne, LR; Coignet, LJA; Zani, VJ; Tsui, LC; Scherer, SW; Dyer, MJS | 1998 | 306 |
| 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 |
| Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor | Osborne, LR; Soder, S; Shi, XM; Pober, B; Costa, T; Scherer, SW; Tsui, L-C | 1997 | 289 |
| Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients | Osborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC | 1996 | 288 |
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