T. Conrad Gilliam
T. Conrad Gilliam
Professor of Genetics University of Chicago
Verified email at bsd.uchicago.edu
Title
Cited by
Cited by
Year
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
29862007
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
28942004
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
15371993
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
14692007
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
9211999
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
7162008
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
6681990
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
6362002
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
5661993
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
4151997
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
4021994
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
3832001
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
3821990
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
3791994
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
3702003
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
3322008
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
3271999
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
3252003
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
3222002
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
3082005
The system can't perform the operation now. Try again later.
Articles 1–20