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Kang, Hyun Min

Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA

TitleYearPMID
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. 2021 33568819
Multiplexed droplet single-cell RNA-sequencing using natural genetic variation. 2018 29227470
A reference panel of 64,976 haplotypes for genotype imputation. 2016 27548312
A global reference for human genetic variation. 2015 26432245
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. 2014 25387710
An integrated map of genetic variation from 1,092 human genomes. 2012 23128226
Evolution and functional impact of rare coding variation from deep sequencing of human exomes. 2012 22604720
Variance component model to account for sample structure in genome-wide association studies. 2010 20208533
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