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Goldstein, David B

Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA

TitleYearPMID
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants. 2021 34183866
Geographical genomics of human leukocyte gene expression variation in southern Morocco. 2010 19966804
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. 2010 20398883
Rare variants create synthetic genome-wide associations. 2010 20126254
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. 2009 19300482
A genome-wide investigation of SNPs and CNVs in schizophrenia. PDF 2009 19197363
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. 2009 19734545
Common genetic variation and human traits. 2009 19369660
Common variants conferring risk of schizophrenia. 2009 19571808
Finding the missing heritability of complex diseases. 2009 19812666
Genome-wide association studies for complex traits: consensus, uncertainty and challenges. 2008 18398418
Large recurrent microdeletions associated with schizophrenia. 2008 18668039
Tissue-specific genetic control of splicing: implications for the study of complex traits. 2008 19222302
WGAViewer: software for genomic annotation of whole genome association studies. 2008 18256235
A whole-genome association study of major determinants for host control of HIV-1. 2007 17641165
In vitro assays fail to predict in vivo effects of regulatory polymorphisms. 2007 17566082
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