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Author Details

Joseph K Pickrell
Gencove Inc.
2003
57
37
PMIDPaper TitleJournal TitlePublished Year
38038370Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates.G3 (Bethesda)2024
37359370Variance component estimates, phenotypic characterization, and genetic evaluation of bovine congestive heart failure in commercial feeder cattle.Front Genet2023
33536225Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays.Genome Res2021
33770507Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations.Am J Hum Genet2021
33743587Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics.BMC Genomics2021
32675347Population genetics of the coral <i>Acropora millepora</i>: Toward genomic prediction of bleaching.Science2020
33167493Assessment of Imputation from Low-Pass Sequencing to Predict Merit of Beef Steers.Genes (Basel)2020
29348143Detecting Polygenic Adaptation in Admixture Graphs.Genetics2018
29965964Correction: The population genetics of human disease: The case of recessive, lethal mutations.PLoS Genet2018
29579179A Bayesian framework for multiple trait colocalization from summary association statistics.Bioinformatics2018
29374253DNA.Land is a framework to collect genomes and phenomes in the era of abundant genetic information.Nat Genet2018
28733365Contrasting Determinants of Mutation Rates in Germline and Soma.Genetics2017
28092683Case-control association mapping by proxy using family history of disease.Nat Genet2017
28957316The population genetics of human disease: The case of recessive, lethal mutations.PLoS Genet2017
28814792Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.Nat Commun2017
28873088Identifying genetic variants that affect viability in large cohorts.PLoS Biol2017
27089181Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Nat Genet2016
26395773Approximately independent linkage disequilibrium blocks in human populations.Bioinformatics2016
27898078Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Nat Genet2016
27681293Erratum: Detection and interpretation of shared genetic influences on 42 human traits.Nat Genet2016
27225129Genome-wide association study identifies 74 loci associated with educational attainment.Nature2016
27463399Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Nat Genet2016
27182965Detection and interpretation of shared genetic influences on 42 human traits.Nat Genet2016
26595274Genome-wide patterns of selection in 230 ancient Eurasians.Nature2015
24352235The complete genome sequence of a Neanderthal from the Altai Mountains.Nature2014
24990677Natural selection for the Duffy-null allele in the recently admixed people of Madagascar.Proc Biol Sci2014
24990607Fast and accurate imputation of summary statistics enhances evidence of functional enrichment.Bioinformatics2014
25168683Toward a new history and geography of human genes informed by ancient DNA.Trends Genet2014
24550290Ancient west Eurasian ancestry in southern and eastern Africa.Proc Natl Acad Sci U S A2014
24702953Joint analysis of functional genomic data and genome-wide association studies of 18 human traits.Am J Hum Genet2014
23410830Inferring admixture histories of human populations using linkage disequilibrium.Genetics2013
24115443Ancient DNA reveals key stages in the formation of central European mitochondrial genetic diversity.Science2013
22344438A systematic survey of loss-of-function variants in human protein-coding genes.Science2012
23166502Inference of population splits and mixtures from genome-wide allele frequency data.PLoS Genet2012
23222792The difficult calls in RNA editing. Interviewed by H Craig Mak.Nat Biotechnol2012
23072811The genetic prehistory of southern Africa.Nat Commun2012
23071454The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels.PLoS Genet2012
22499788Misuse of hierarchical linear models overstates the significance of a reported association between OXTR and prosociality.Proc Natl Acad Sci U S A2012
22307276DNaseâ¿¿I sensitivity QTLs are a major determinant of human expression variation.Nature2012
22207615Comparative RNA sequencing reveals substantial genetic variation in endangered primates.Genome Res2012
22422963Comment on "Widespread RNA and DNA sequence differences in the human transcriptome".Science2012
22359548Exon-specific QTLs skew the inferred distribution of expression QTLs detected using gene expression array data.PLoS One2012
21251332DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines.Genome Biol2011
21690102False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions.Bioinformatics2011
19942252A rod cell marker of nocturnal ancestry.J Hum Evol2010
21151575Noisy splicing drives mRNA isoform diversity in human cells.PLoS Genet2010
20532200The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate.PLoS Genet2010
20220758Understanding mechanisms underlying human gene expression variation with RNA sequencing.Nature2010
20178769The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation.Curr Biol2010
19307593Signals of recent positive selection in a worldwide sample of human populations.Genome Res2009
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University Medical Center Groningen, University of Groningen
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King's College London
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Rush University Medical Center
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University of Bonn, School of Medicine & University Hospital Bonn.
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