arrow
返回
T

T. Conrad Gilliam

university of chicago

62H指数
205论文数
2.2W被引数
收录论文 55
发表时间
Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources
err2019-06-03
err21
errOAAI
errSulakhe, Dinanath; D'Souza, Mark; Wang, Sheng; Balasubramanian, Sandhya; Athri, Prashanth; Xie, Bingqing; Canzar, Stefan; Agam, Gady; Gilliam, T. Conrad; Maltsev, Natalia
err分享
err收藏
Lynx: a knowledge base and an analytical workbench for integrative medicine
err2015-11-20
err8
errOAAI
errSulakhe, 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
err分享
err收藏
Lynx web services for annotations and systems analysis of multi-gene disorders
err2014-06-19
err6
errOAAI
errSulakhe, Dinanath; Taylor, Andrew; Balasubramanian, Sandhya; Feng, Bo; Xie, Bingqing; Bornigen, Daniela; Dave, Utpal J.; Foster, Ian T.; Gilliam, T. Conrad; Maltsev, Natalia
err分享
err收藏
Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR)
err2008-07-29
err64
errOAAI
errStrug, L. J.; Suresh, R.; Fyer, A. J.; Talati, A.; Adams, P. B.; Li, W.; Hodge, S. E.; Gilliam, T. C.; Weissman, M. M.
err分享
err收藏
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
err2008-06-01
err247
errOAAI
errChristian, 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.
err分享
err收藏
Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network
err2008-04-16
err60
errOAAI
errIossifov, Ivan; Zheng, Tian; Baron, Miron; Gilliam, T. Conrad; Rzhetsky, Andrey
err分享
err收藏
Recurrent 16p11.2 microdeletions in autism
err2007-11-07
err642
errOAAI
errKumar, 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.
err分享
err收藏
Mapping complex traits in diseases of the hair and skin
err2007-05-04
err15
errOAAI
errAita, VM; Christiano, AM; Gilliam, TC
err分享
err收藏
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata
err2007-02-01
err112
errOAAI
errMartinez-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.
err分享
err收藏
DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability
err2007-02-01
err86
PREAI
errXu, Haiyan; Kellendonk, Christoph B.; Simpson, Eleanor H.; Keilp, John G.; Bruder, Gerard E.; Polan, H. Jonathan; Kandel, Eric R.; Gilliam, T. Conrad
err分享
err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
err2006-01-10
err137
PREAI
errCheng, 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
err分享
err收藏
Catechol-O-methyltransferase (COMT) genotypes and working memory: Associations with differing cognitive operations
err2005-12-01
err242
PREAI
errBruder, GE; Keilp, JG; Xu, HY; Shikhman, M; Schori, E; Gorman, JM; Gilliam, TC
err分享
err收藏
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q
err2005-10-01
err197
errOAAI
errMcQueen, 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
err分享
err收藏
Psychosis and the genetic spectrum of bipolar disorder: evidence from linkage analysis
err2005-09-26
err5
errOAAI
errCheng, R; Park, N; Juo, SH; Liu, J; Loth, JE; Endicott, J; Gilliam, TC; Baron, M
err分享
err收藏
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
err2005-04-12
err110
PREAI
errAlarcón, M; Yonan, AL; Gilliam, TC; Cantor, RM; Geschwind, DH
err分享
err收藏
Evidence for sex-specific risk alleles in autism spectrum disorder
err2004-12-01
err161
errOAAI
errStone, JL; Merriman, B; Cantor, RM; Yonan, AL; Gilliam, TC; Geschwind, DH; Nelson, SF
err分享
err收藏
Absence of psychosis may influence linkage results for bipolar disorder
err2004-11-30
err3
errOAAI
errPark, N; Cheng, R; Juo, SH; Liu, J; Loth, JE; Endicott, J; Gilliam, TC; Baron, M
err分享
err收藏
Arm tremor secondary to Wilson's disease
err2004-11-04
err4
PREAI
errFrucht, S; Sun, D; Schiff, N; Eidelberg, D; Gilliam, TC
err分享
err收藏
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy
err2004-10-08
err60
PREAI
errWilhelmsen, 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
err分享
err收藏