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Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits

American journal of human genetics, 2014-04, Vol.94 (4), p.559-573

Pickrell, Joseph K.

2014

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Inference of population splits and mixtures from genome-wide allele frequency data

PLoS genetics, 2012-11, Vol.8 (11), p.e1002967-e1002967

2012

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Approximately independent linkage disequilibrium blocks in human populations

Bioinformatics (Oxford, England), 2016-01, Vol.32 (2), p.283-285

2016

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Detection and interpretation of shared genetic influences on 42 human traits

Nature genetics, 2016-07, Vol.48 (7), p.709-717

2016

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Case–control association mapping by proxy using family history of disease

Nature genetics, 2017-03, Vol.49 (3), p.325-331

2017

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The Genetics of Human Adaptation: Hard Sweeps, Soft Sweeps, and Polygenic Adaptation

Current biology, 2010-02, Vol.20 (4), p.R208-R215

2010

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Detecting Polygenic Adaptation in Admixture Graphs

Genetics (Austin), 2018-04, Vol.208 (4), p.1565-1584

2018

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Inferring admixture histories of human populations using linkage disequilibrium

Genetics (Austin), 2013-04, Vol.193 (4), p.1233-1254

2013

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Noisy splicing drives mRNA isoform diversity in human cells

PLoS genetics, 2010-12, Vol.6 (12), p.e1001236-e1001236

2010

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Ancient west Eurasian ancestry in southern and eastern Africa

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (7), p.2632-2637

2014

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Comment on "Widespread RNA and DNA sequence differences in the human transcriptome"

Science (American Association for the Advancement of Science), 2012-03, Vol.335 (6074), p.1302; author reply 1302-1302

2012

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DNase I sensitivity QTLs are a major determinant of human expression variation

Nature (London), 2012-02, Vol.482 (7385), p.390-394

2012

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Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data

Bioinformatics, 2009-12, Vol.25 (24), p.3207-3212

2009

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Identifying genetic variants that affect viability in large cohorts

PLoS biology, 2017-09, Vol.15 (9), p.e2002458-e2002458

2017

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Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

Nature communications, 2017-08, Vol.8 (1), p.266-10, Article 266

2017

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Signals of recent positive selection in a worldwide sample of human populations

Genome Research, 2009-05, Vol.19 (5), p.826-837

2009

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The role of geography in human adaptation

PLoS genetics, 2009-06, Vol.5 (6), p.e1000500-e1000500

2009

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Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics

BMC genomics, 2021-03, Vol.22 (1), p.197-197, Article 197

2021

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Evolutionary dynamics of human Toll-like receptors and their different contributions to host defense

PLoS genetics, 2009-07, Vol.5 (7), p.e1000562-e1000562

2009

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The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels

PLoS genetics, 2012-10, Vol.8 (10), p.e1003000-e1003000

2012

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Toward a new history and geography of human genes informed by ancient DNA

Trends in genetics, 2014-09, Vol.30 (9), p.377-389

2014

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Comparative RNA sequencing reveals substantial genetic variation in endangered primates

Genome research, 2012-04, Vol.22 (4), p.602-610

2012

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False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions

Bioinformatics, 2011-08, Vol.27 (15), p.2144-2146

2011

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Variance component estimates, phenotypic characterization, and genetic evaluation of bovine congestive heart failure in commercial feeder cattle

Frontiers in genetics, 2023-06, Vol.14, p.1148301-1148301

2023

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Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays

Genome research, 2021-04, Vol.31 (4), p.529-537

2021

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Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits

Inference of population splits and mixtures from genome-wide allele frequency data

Approximately independent linkage disequilibrium blocks in human populations

Detection and interpretation of shared genetic influences on 42 human traits

Case–control association mapping by proxy using family history of disease

The Genetics of Human Adaptation: Hard Sweeps, Soft Sweeps, and Polygenic Adaptation

Detecting Polygenic Adaptation in Admixture Graphs

Inferring admixture histories of human populations using linkage disequilibrium

Noisy splicing drives mRNA isoform diversity in human cells

Ancient west Eurasian ancestry in southern and eastern Africa

Comment on "Widespread RNA and DNA sequence differences in the human transcriptome"

DNase I sensitivity QTLs are a major determinant of human expression variation

Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data

Identifying genetic variants that affect viability in large cohorts

Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

Signals of recent positive selection in a worldwide sample of human populations

The role of geography in human adaptation

Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics

Evolutionary dynamics of human Toll-like receptors and their different contributions to host defense

The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels

Toward a new history and geography of human genes informed by ancient DNA

Comparative RNA sequencing reveals substantial genetic variation in endangered primates

False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions

Variance component estimates, phenotypic characterization, and genetic evaluation of bovine congestive heart failure in commercial feeder cattle

Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays

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