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Showing results 60 to 79 of 110 < previous next >

Title	Author(s)	Issue Date
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
Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents Journal:Human Molecular Genetics	Thacker, J Tambini, CE Simpson, PJ Tsui, LC Scherer, SW	1995
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas Journal:Oncogene	Zeng, WR Scherer, SW Koutsilieris, M Huizenga, JJ Filteau, F Tsui, LC Nepveu, A	1997
MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinoma Journal:Cell	Eppert, K Scherer, SW Ozcelik, H Pirone, R Hoodless, P Kim, H Tsui, LC Bapat, B Gallinger, S Andrulis, IL Thomsen, GH Wrana, JL Attisano, L	1996
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12 Journal:Genomics	Egan, S Herbrick, JA Tsui, LC Cohen, B Flock, G Beatty, B Scherer, SW	1998
Mapping the midkine family of developmentally regulated signaling molecules Journal:Mammalian Genome	Peichel, CL Scherer, SW Tsui, LC Beier, DR Vogt, TF	1993
Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre) Journal:Human Molecular Genetics	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
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site Journal:Proceedings of the National Academy of Sciences of the United States of America	Mishmar, D Rahat, A Scherer, SW Nyakatura, G Hinzmann, B Kohwi, Y MandelGutfroind, Y Lee, JR Drescher, B Sas, DE Margalit, H Platzer, M Weiss, A Tsui, LC Rosenthal, A Kerem, B	1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders Journal:Blood	Döhner, K Brown, J Hehmann, U Hetzel, C Stewart, J Lowther, G Scholl, C Fröhling, S Cuneo, A Tsui, LC Lichter, P Scherer, SW Döhner, H	1998
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias Journal:Blood	Fischer, K Fröhling, S Scherer, SW Brown, JM Scholl, C Stilgenbauer, S Tsui, LC Lichter, P Döhner, H	1997
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia Journal:Blood	Johnson, EJ Scherer, SW Osborne, L Tsui, LC Oscier, D Mould, S Cotter, FE	1996
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C Journal:BMC Medical Genomics	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
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy Journal:Nature Genetics	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
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly Journal:Human Molecular Genetics	Roessler, E Belloni, E Gaudenz, K Vargas, F Scherer, SW Tsui, LC Muenke, M	1997
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Journal:Nature genetics	Roessler, E Belloni, E Gaudenz, K Jay, P Berta, P Scherer, SW Tsui, LC Muenke, M	1996

Showing results 60 to 79 of 110 < previous next >