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Title	Author(s)	Issue Date
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
Heterogeneity of the autosomal dominant split hand/split foot malformation [6] Journal:American Journal of Human Genetics	Zlotogora, J Evans, JP Palmer, S Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K	1995
A human Chromosome 7-specific genomic DNA library in yeast artificial chromosomes Journal:Mammalian Genome	Scherer, SW Tompkins, BJF Tsui, LC	1992
Human chromosome 7: DNA sequence and biology Journal:Science	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
Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis Journal:Nature Genetics	Abecasis, G Tam, PKH Bustamante, CD Ostrander, EA Scherer, SW Chanock, SJ Kwok, PY Brookes, AJ	2007
The human metabotropic glutamate receptor 8 (GRM8) gene: A disproportionately large gene located at 7q31.3-q32.1 Journal:Genomics	Scherer, SW Soder, S Duvoisin, RM Huizenga, JJ Tsui, LC	1997
Human PON2 gene at 7q21.3: Cloning, multiple mRNA forms, and missense polymorphisms in the coding sequence Journal:Gene	Mochizuki, H Scherer, SW Xi, T Nickle, DC Majer, M Huizenga, JJ Tsui, LC Prochazka, M	1998
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas Journal:Oncogene	Edelson, MI Scherer, SW Tsui, LC Welch, WR Bell, DA Berkowitz, RS Mok, SC	1997
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome Journal:Genomics	Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC	1999
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient Journal:American Journal of Human Genetics	Alley, TL Gray, BA Lee, SH Scherer, SW Tsui, LC Tint, GS Williams, CA Zori, R Wallace, MR	1995
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients Journal:Genomics	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
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Journal:Nature genetics	Belloni, E Muenke, M Roessler, E Traverso, G SiegelBartelt, J Frumkin, A Mitchell, HF DonisKeller, H Helms, C Hing, AV Heng, HH Koop, B Martindale, D Rommens, JM Tsui, LC Scherer, SW	1996
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31 Journal:Genomics	Cheung, J Petek, E Nakabayashi, K Tsui, LC Vincent, JB Scherer, SW	2001
Involvement of the HLXB9 homeobox gene in Currarino syndrome [2] Journal:American Journal of Human Genetics	Belloni, E Martucciello, G Verderio, D Ponti, E Seri, M Jasonni, V Torre, M Ferrari, M Tsui, LC Scherer, SW	2000
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism Journal:Cell	Sattterstrom, FK Kosmicki, JA Wang, J Breen, MS De Rubeis, S An, JY Peng, M Collins, R Grove, J Klei, L Stevens, C Pedersen, CB Pedersen, MG Poterba, T Poulsen, JB Ripke, S Schork, AJ Thompson, WK Turley, P Walters, RK Brand, H Montenegro, EMS Schwartz, G Nguyen, R Guerrero, EE Dias, C Betancur, C Cook, EH Gallagher, L Gill, M Sutcliffe, JS Thurm, A Moreira, D Zwick, ME Borglum, AD State, MW Cicek, AE Talkowski, ME Cutler, DJ Devlin, B Sanders, SJ Roeder, K Daly, MJ Morrow, EM Buxbaum, JD Aleksic, B Anney, R Barbosa, M Bishop, S Brusco, A Bybjerg-Grauholm, J Carracedo, A Chan, MCY Chiocchetti, AG Mors, O Chung, BHY Coon, H Cuccaro, ML Curro, A Dalla Bernardina, B Doan, R Domenici, E Dong, S Fallerini, C Fernandez-Prieto, M Mortensen, PB Ferrero, GM Freitag, CM Fromer, M Gargus, JJ Geschwind, D Giorgio, E Gonzalez-Perias, J Guter, S Halpern, D Hansen-Kiss, E Mosconi, M He, X Herman, GE Hertz-Piccfiotto, I Hougaard, DM Hultman, CM Ionita-Laza, L Jacob, S Jamison, J Jugessur, A Kaartinen, M Muglia, P Knudsen, GP Kolevzon, A Kushima, I Lee, SL Lehtimaki, T Lim, ET Lintas, C Lipkin, WI Lopergolo, D Lopes, F Neale, BM Ludena, Y Maciel, P Magnus, P Mahjani, B Maltman, N Manoach, DS Meiri, G Menashe, I Miller, J Minshew, N Nordentoft, M Ozaki, N Reichert, J Palotie, A Parellada, M Passos-Bueno, MR Pericak-Vance, M Persico, AM Pessah, I Puura, K Reichenberg, A Renien, A Riberi, E Mulhern, MS Robinson, EB Samocha, KE Sandin, S Santangelo, SI Schellenberg, G Scherer, SW Schlitt, S Schmidt, R Schmitt, L Silva, IMW Artomov, M Singh, T Siper, PM Smith, M Soares, G Stoltenberg, C Suren, P Susser, E Sweeney, J Szatmari, P Tang, L Gerges, S Tassone, F Teufel, K Trabetti, E Trelles, MDP Walsh, CA Weiss, LA Werge, T Werling, DM Wigdor, EM Wilkinson, E Sheppard, S Willsey, AJ Yu, TW YU, HC Yuen, R Zachi, E Agerbo, E Als, TD Appadurai, V Baekvad-Hansen, M Belliveau, R Xu, X Buil, A Carey, CE Cerrato, F Chambert, K Churchhouse, C Dalsgaard, S Demontis, D Dumont, A Goldstein, J Hansen, CS Bhaduri, A Hauberg, ME Hollegaard, MV Howrigan, DP Huang, H Maller, J Martin, AR Martin, J Mattheisen, M Moran, J Pallesen, J Norman, U Palmer, DS	2020
Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1 Journal:Genomics	Torigoe, K Harada, T Kusaba, H Uchiumi, T Kohno, K Green, ED Scherer, SW Tsui, LC Schlessinger, D Kuwano, M Wada, M	1998
Localization of the gene encoding the α 2/δ-subunits of the L-type voltage dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families Journal:Human Molecular Genetics	Iles, DE LehmannHorn, F Scherer, SW Tsui, LC Weghuis, DO Suijkerbuijk, RF Heytens, L Mikala, G Schwartz, A Ellis, FR Stewart, AD Deufel, T Wieringa, B	1994
Localization of the gene encoding the α2/δ subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21- q22 by somatic cell hybrid analysis Journal:Genomics	Powers, PA Scherer, SW Tsui, LC Gregg, RG Hogan, K	1994
Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31→q32 Journal:Cytogenetics and Cell Genetics	Scherer, SW Otulakowski, G Robinson, BH Tsui, LC	1991
Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q Journal:Genomics	Scherer, SW Duvoisin, RM Kuhn, R Heng, HHQ Belloni, E Tsui, LC	1996

Showing results 46 to 65 of 110 < previous next >