未登录Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources
Sulakhe, Dinanath; D'Souza, Mark; Wang, Sheng; Balasubramanian, Sandhya; Athri, Prashanth; Xie, Bingqing; Canzar, Stefan; Agam, Gady; Gilliam, T. Conrad; Maltsev, Natalia
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收藏Lynx: a knowledge base and an analytical workbench for integrative medicine
Sulakhe, Dinanath; Xie, Bingqing; Taylor, Andrew; D'Souza, Mark; Balasubramanian, Sandhya; Hashemifar, Somaye; White, Steven; Dave, Utpal J.; Agam, Gady; Xu, Jinbo; Wang, Sheng; Gilliam, T. Conrad; Maltsev, Natalia
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收藏Lynx web services for annotations and systems analysis of multi-gene disorders
Sulakhe, Dinanath; Taylor, Andrew; Balasubramanian, Sandhya; Feng, Bo; Xie, Bingqing; Bornigen, Daniela; Dave, Utpal J.; Foster, Ian T.; Gilliam, T. Conrad; Maltsev, Natalia
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收藏Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
Christian, Susan L.; Brune, Camille W.; Sudi, Jyotsna; Kumar, Ravinesh A.; Liu, Shaung; Karamohamed, Samer; Badner, Judith A.; Matsui, Seiichi; Conroy, Jeffrey; McQuaid, Devin; Gergel, James; Hatchwell, Eli; Gilliam, T. Conrad; Gershon, Elliot S.; Nowak, Norma J.; Dobyns, William B.; Cook, Edwin H., Jr.
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收藏Recurrent 16p11.2 microdeletions in autism
Kumar, Ravinesh A.; KaraMohamed, Samer; Sudi, Jyotsna; Conrad, Donald F.; Brune, Camille; Badner, Judith A.; Gilliam, T. Conrad; Nowak, Norma J.; Cook, Edwin H., Jr.; Dobyns, William B.; Christian, Susan L.
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收藏Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata
Martinez-Mir, Amalia; Zlotogorski, Abraham; Gordon, Derek; Petukhova, Lynn; Mo, Jianhong; Gilliam, T. Conrad; Londono, Douglas; Haynes, Chad; Ott, Jurg; Hordinsky, Maria; Nanova, Krassimira; Norris, David; Price, Vera; Duvic, Madeleine; Christiano, Angela M.
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收藏Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder
Cheng, R; Juo, SH; Loth, JE; Nee, J; Iossifov, I; Blumenthal, R; Sharpe, L; Kanyas, K; Lerer, B; Lilliston, B; Smith, M; Trautman, K; Gilliam, TC; Endicott, J; Baron, M
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收藏Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q
McQueen, MB; Devlin, B; Faraone, SV; Nimgaonkar, VL; Sklar, P; Smoller, JW; Jamra, RA; Albus, M; Bacanu, SA; Baron, M; Barrett, TB; Berrettini, W; Blacker, D; Byerley, W; Cichon, S; Coryell, W; Craddock, N; Daly, MJ; DePaulo, JR; Edenberg, HJ; Foroud, T; Gill, M; Gilliam, TC; Hamshere, M; Jones, I; Jones, L; Juo, SH; Kelsoe, JR; Lambert, D; Lange, C; Lerer, B; Liu, JJ; Maier, W; MacKinnon, JD; McInnis, MG; McMahon, FJ; Murphy, DL; Nöthen, MM; Nurnberger, JI; Pato, CN; Pato, MT; Potash, JB; Propping, P; Pulver, AE; Rice, JP; Rietschel, M; Scheftner, W; Schumacher, J; Segurado, R; Van Steen, K; Xie, WT; Zandi, PP; Laird, NM
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收藏Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy
Wilhelmsen, KC; Blake, DM; Lynch, T; Mabutas, J; DeVera, M; Neystat, M; Bernstein, M; Hirano, M; Gilliam, TC; Murphy, PL; Sola, MD; Bonilla, E; Schotland, DL; Hays, AP; Rowland, LP
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