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Gabriel, Stacey B

Broad Institute of MIT and Harvard, Program in Medical and Population Genetics, Cambridge, MA, USA

TitleYearPMID
Analysis of protein-coding genetic variation in 60,706 humans. 2016 27535533
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. 2012 22511880
Integrating common and rare genetic variation in diverse human populations. 2010 20811451
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. 2008 18711365
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. 2008 18776909
A second generation human haplotype map of over 3.1 million SNPs. 2007 17943122
Efficiency and power in genetic association studies. 2005 16244653
The structure of haplotype blocks in the human genome. 2002 12029063
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