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Li, Yun

Department of Genetics, University of North Carolina, Chapel Hill, North Carolina, United States of America

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
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. 2018 29700475
Efficient derivation of microglia-like cells from human pluripotent stem cells. 2016 27668937
A comparison of approaches to account for uncertainty in analysis of imputed genotypes. 2011 21254217
Rare-variant association testing for sequencing data with the sequence kernel association test. 2011 21737059
Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals. 2010 21129726
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. 2010 21058334
METAL: fast and efficient meta-analysis of genomewide association scans. 2010 20616382
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. 2010 20081858
Genotype imputation. 2009 19715440
Genotype-imputation accuracy across worldwide human populations. 2009 19215730
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. 2008 18372903
Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 2008 18193043
A second generation human haplotype map of over 3.1 million SNPs. 2007 17943122
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