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Raffield, Laura M

Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

TitleYearPMID
A saturated map of common genetic variants associated with human height. 2022 36224396
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. 2019 31869403
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