Cantor rm
Cantor rm
Professor of Human Genetics
Verified email at mednet.ucla.edu
Title
Cited by
Cited by
Year
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
18902010
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
17012013
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
16712009
Genome-wide association study identifies five new schizophrenia loci
S Ripke, AR Sanders, KS Kendler, DF Levinson, P Sklar, PA Holmans, ...
Nature genetics 43 (10), 969, 2011
15922011
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
14612014
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
14352007
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
I Voineagu, X Wang, P Johnston, JK Lowe, Y Tian, S Horvath, J Mill, ...
Nature 474 (7351), 380-384, 2011
13982011
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...
Neuron 70 (5), 863-885, 2011
11632011
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
9672009
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
M Alarcón, BS Abrahams, JL Stone, JA Duvall, JV Perederiy, JM Bomar, ...
The American Journal of Human Genetics 82 (1), 150-159, 2008
8632008
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...
Neuron 87 (6), 1215-1233, 2015
8092015
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
6502009
Prioritizing GWAS results: a review of statistical methods and recommendations for their application
RM Cantor, K Lange, JS Sinsheimer
The American Journal of Human Genetics 86 (1), 6-22, 2010
6432010
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
5862010
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
5812012
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
5552018
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
5342015
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
4532014
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ...
Brain imaging and behavior 8 (2), 153-182, 2014
4162014
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ...
PLoS Genet 5 (6), e1000536, 2009
4132009
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