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Gupta, Namrata

Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA

TitleYearPMID
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
Analysis of protein-coding genetic variation in 60,706 humans. 2016 27535533
Exome sequencing and the genetic basis of complex traits. 2012 22641211
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies. 2012 22610117
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