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Title	Author(s)	Issue Date	Views
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1	Scherer, SW Poorkaj, P Allen, T Kim, J Geshuri, D Nunes, M Soder, S Stephens, K Pagon, RA Patton, MA Berg, MA Donlon, T Rivera, H Pfeiffer, RA Naritomi, K Hughes, H Genuardi, M Gurrieri, F Neri, G Lovrein, E Magenis, E Tsui, L-C Evans, JP	1994	121
Fine mapping of the human and mouse genes for the type i procollagen COOH-terminal proteinase enhancer protein Journal:Genomics	Takahara, K Osborne, L Elliott, RW Tsui, LC Scherer, SW Greenspan, DS	1996	155
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6 Journal:Mammalian Genome	Crackower, MA Heng, HHQ Shi, X Scherer, SW Tsui, LC	1997	130
Functional impact of global rare copy number variation in autism spectrum disorders Journal:Nature	Pinto, D Pagnamenta, AT Klei, L Anney, R Merico, D Regan, R Conroy, J Magalhaes, TR Correia, C Abrahams, BS Almeida, J Bacchelli, E Bader, GD Bailey, AJ Baird, G Battaglia, A Berney, T Bolshakova, N Bölte, S Bolton, PF Bourgeron, T Brennan, S Brian, J Bryson, SE Carson, AR Casallo, G Casey, J Chung, BHY Cochrane, L Corsello, C Crawford, EL Crossett, A Cytrynbaum, C Dawson, G De Jonge, M Delorme, R Drmic, I Duketis, E Duque, F Estes, A Farrar, P Fernandez, BA Folstein, SE Fombonne, E Freitag, CM Gilbert, J Gillberg, C Glessner, JT Goldberg, J Green, A Green, J Guter, SJ Hakonarson, H Heron, EA Hill, M Holt, R Howe, JL Hughes, G Hus, V Igliozzi, R Kim, C Klauck, SM Kolevzon, A Korvatska, O Kustanovich, V Lajonchere, CM Lamb, JA Laskawiec, M Leboyer, M Le Couteur, A Leventhal, BL Lionel, AC Liu, XQ Lord, C Lotspeich, L Lund, SC Maestrini, E Mahoney, W Mantoulan, C Marshall, CR Mcconachie, H Mcdougle, CJ Mcgrath, J Mcmahon, WM Merikangas, A Migita, O Minshew, NJ Mirza, GK Munson, J Nelson, SF Noakes, C Noor, A Nygren, G Oliveira, G Papanikolaou, K Parr, JR Parrini, B Paton, T Pickles, A Pilorge, M Piven, J Ponting, CP Posey, DJ Poustka, A Poustka, F Prasad, A Ragoussis, J Renshaw, K Rickaby, J Roberts, W Roeder, K Roge, B Rutter, ML Bierut, LJ Rice, JP Salt, J Sansom, K Sato, D Segurado, R Sequeira, AF Senman, L Shah, N Sheffield, VC Soorya, L Sousa, I Stein, O Sykes, N Stoppioni, V Strawbridge, C Tancredi, R Tansey, K Thiruvahindrapduram, B Thompson, AP Thomson, S Tryfon, A Tsiantis, J Van Engeland, H Vincent, JB Volkmar, F Wallace, S Wang, K Wang, Z Wassink, TH Webber, C Weksberg, R Wing, K Wittemeyer, K Wood, S Wu, J Yaspan, BL Zurawiecki, D Zwaigenbaum, L Buxbaum, JD Cantor, RM Cook, EH Coon, H Cuccaro, ML Devlin, B Ennis, S Gallagher, L Geschwind, DH Gill, M Haines, JL Hallmayer, J Miller, J Monaco, AP Nurnberger Jr, JI Paterson, AD PericakVance, MA Schellenberg, GD Szatmari, P Vicente, AM Vieland, VJ Wijsman, EM Scherer, SW Sutcliffe, JS Betancur, C	2010	98
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia Journal:Nature Genetics	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	183
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein Journal:Nature Genetics	Kobayashi, K Sinasac, DS Iijima, M Boright, AP Begum, L Lee, JR Yasuda, T Ikeda, S Hirano, R Terazono, H Crackower, MA Kondo, I Tsui, LC Scherer, SW Saheki, T	1999	184
Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin γ-subunit gene (GNGT1) Journal:Genomics	Scherer, SW Feinstein, DS Oliveira, L Tsui, LC Pittler, SJ	1996	168
Gene structure of the human MET proto-oncogene Journal:Oncogene	Duh, FM Scherer, SW Tsui, LC Lerman, MI Zbar, B Schmidt, L	1997	185
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus Journal:Genome	Hwang, MY Kang, YJ Kim, YH Scherer, SW Tsui, LC Sohn, U	1999	158
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites Journal:Atherosclerosis	Boright, AP Connelly, PW Brunt, JH Scherer, SW Tsui, LC Hegele, RA	1998	123
Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree Journal:Clinical Genetics	Hegele, RA Harris, SB Connelly, PW Hanley, AJG Tsui, LC Zinman, B Scherer, SW	1998	108
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Journal:Genome biology	Cheung, J Estivill, X Khaja, R MacDonald, JR Lau, K Tsui, LC Scherer, SW	2003	121
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue Journal:Genomics	Sinasac, DS Crackower, MA Lee, JR Kobayashi, K Saheki, T Scherer, SW Tsui, LC	1999	182
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas Journal:Nature genetics	Schmidt, L Duh, FM Chen, F Kishida, T Glenn, G Choyke, P Scherer, SW Zhuang, Z Lubensky, I Dean, M Allkimets, R Chidambaram, A Bergerheim, UR Feltis, JT Casadevall, C Zamarron, A Bernues, M Richard, S Lips, CJM Walther, MM Tsui, L-C Geil, L Orcutt, ML Stackhouse, T Lipan, J Slife, L Brauch, H Decker, J Niehans, G Hughson, MD Moch, H Storkel, S Lerman, MI Linehan, WM Zbar, B	1997	234
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	106
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	131
A human Chromosome 7-specific genomic DNA library in yeast artificial chromosomes Journal:Mammalian Genome	Scherer, SW Tompkins, BJF Tsui, LC	1992	150
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	217
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	162
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	122

Showing results 32 to 51 of 110 < previous next >