T. Conrad Gilliam
T. Conrad Gilliam
Professor of Genetics University of Chicago
Verified email at bsd.uchicago.edu
Cited by
Cited by
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
Large-scale copy number polymorphism in the human genome
J Sebat, B Lakshmi, J Troge, J Alexander, J Young, P Lundin, S Månér, ...
Science 305 (5683), 525-528, 2004
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
RE Tanzi, K Petrukhin, I Chernov, JL Pellequer, W Wasco, B Ross, ...
Nature genetics 5 (4), 344-350, 1993
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21
VM Aita, XH Liang, V Murty, DL Pincus, W Yu, E Cayanis, S Kalachikov, ...
Genomics 59 (1), 59-65, 1999
Recurrent 16p11. 2 microdeletions in autism
RA Kumar, S KaraMohamed, J Sudi, DF Conrad, C Brune, JA Badner, ...
Human molecular genetics 17 (4), 628-638, 2008
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
LM Brzustowicz, T Lehner, LH Castilla, GK Penchaszadeh, ...
Nature 344 (6266), 540-541, 1990
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
S Kalachikov, O Evgrafov, B Ross, M Winawer, C Barker-Cummings, ...
Nature genetics 30 (3), 335-341, 2002
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
K Petrukhin, SG Fischer, M Pirastu, RE Tanzi, I Chernov, M Devoto, ...
Nature genetics 5 (4), 338-343, 1993
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses
AB Shah, I Chernov, HT Zhang, BM Ross, K Das, S Lutsenko, E Parano, ...
The American Journal of Human Genetics 61 (2), 317-328, 1997
Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions
K Petrukhin, S Lutsenko, I Chernov, BM Ross, JH Kaplan, TC Gilliam
Human Molecular Genetics 3 (9), 1647-1656, 1994
A genomewide screen for autism susceptibility loci
J Liu, DR Nyholt, P Magnussen, E Parano, P Pavone, D Geschwind, ...
The American Journal of Human Genetics 69 (2), 327-340, 2001
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy
TC Gilliam, LM Brzustowicz, LH Castilla, T Lehner, GK Penchaszadeh, ...
Nature 345 (6278), 823-825, 1990
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22. 3
RE Straub, T Lehner, Y Luo, JE Loth, W Shao, L Sharpe, JR Alexander, ...
Nature genetics 8 (3), 291-296, 1994
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris
A Kljuic, H Bazzi, JP Sundberg, A Martinez-Mir, R O'Shaughnessy, ...
Cell 113 (2), 249-260, 2003
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
SL Christian, CW Brune, J Sudi, RA Kumar, S Liu, S Karamohamed, ...
Biological psychiatry 63 (12), 1111-1117, 2008
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8
S Ranta, Y Zhang, B Ross, L Lonka, E Takkunen, A Messer, J Sharp, ...
Nature genetics 23 (2), 233-236, 1999
A genomewide screen of 345 families for autism-susceptibility loci
AL Yonan, M Alarcon, R Cheng, PKE Magnusson, SJ Spence, AA Palmer, ...
The American Journal of Human Genetics 73 (4), 886-897, 2003
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
M Alarcón, RM Cantor, J Liu, TC Gilliam, DH Geschwind, ...
The American Journal of Human Genetics 70 (1), 60-71, 2002
Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations
GE Bruder, JG Keilp, H Xu, M Shikhman, E Schori, JM Gorman, TC Gilliam
Biological psychiatry 58 (11), 901-907, 2005
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