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Heinzen, Erin L

Duke University, Center for Human Genome Variation, School of Medicine, Durham, NC, USA

TitleYearPMID
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. 2010 20398883
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
Tissue-specific genetic control of splicing: implications for the study of complex traits. 2008 19222302
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