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Contrasting X-Linked and Autosomal Diversity across 14 Human Populations

American journal of human genetics, 2014-06, Vol.94 (6), p.827-844

2014

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Human population differentiation is strongly correlated with local recombination rate

PLoS genetics, 2010-03, Vol.6 (3), p.e1000886

2010

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XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome

The Journal of heredity, 2015, Vol.106 (5), p.666-671

2015

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Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

Nature genetics, 2007-10, Vol.39 (10), p.1251-1255

2007

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Principal component analysis characterizes shared pathogenetics from genome-wide association studies

PLoS computational biology, 2014-09, Vol.10 (9), p.e1003820-e1003820

2014

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Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases

PloS one, 2014-12, Vol.9 (12), p.e113684-e113684

2014

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NRE: a tool for exploring neutral loci in the human genome

BMC bioinformatics, 2012-11, Vol.13 (1), p.301-301, Article 301

2012

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Gene-based testing of interactions in association studies of quantitative traits

PLoS genetics, 2013-02, Vol.9 (2), p.e1003321-e1003321

2013

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The history of African gene flow into Southern Europeans, Levantines, and Jews

PLoS genetics, 2011-04, Vol.7 (4), p.e1001373-e1001373

2011

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Accelerated genetic drift on chromosome X during the human dispersal out of Africa

Nature genetics, 2009-01, Vol.41 (1), p.66-70

2009

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Incomplete Lineage Sorting and Hybridization Statistics for Large-Scale Retroposon Insertion Data

PLoS computational biology, 2016-03, Vol.12 (3), p.e1004812-e1004812

2016

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Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits

Frontiers in genetics, 2019-04, Vol.10, p.271-271

2019

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Extracting replicable associations across multiple studies: Empirical Bayes algorithms for controlling the false discovery rate

PLoS computational biology, 2017-08, Vol.13 (8), p.e1005700-e1005700

2017

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Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation

PLoS computational biology, 2012-07, Vol.8 (7), p.e1002600-e1002600

2012

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Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations

PLoS genetics, 2012-05, Vol.8 (5), p.e1002714-e1002714

2012

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Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels

PloS one, 2014-03, Vol.9 (3), p.e92469-e92469

2014

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Enhanced methods for local ancestry assignment in sequenced admixed individuals

PLoS computational biology, 2014-04, Vol.10 (4), p.e1003555-e1003555

2014

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Gene-Based Nonparametric Testing of Interactions Using Distance Correlation Coefficient in Case-Control Association Studies

Genes, 2018-12, Vol.9 (12), p.608

2018

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Human dominant disease genes are enriched in paralogs originating from whole genome duplication

PLoS computational biology, 2014-07, Vol.10 (7), p.e1003754-e1003754

2014

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The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry

PloS one, 2016-03, Vol.11 (3), p.e0152056-e0152056

2016

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Explosive genetic evidence for explosive human population growth

Current opinion in genetics & development, 2016-12, Vol.41, p.130-139

2016

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Historical pedigree reconstruction from extant populations using PArtitioning of RElatives (PREPARE)

PLoS computational biology, 2014-06, Vol.10 (6), p.e1003610-e1003610

2014

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Comments on "Human dominant disease genes are enriched in paralogs originating from whole genome duplication"

PLoS computational biology, 2014-07, Vol.10 (7), p.e1003758-e1003758

2014

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Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions

PloS one, 2015-03, Vol.10 (3), p.e0121644-e0121644

2015

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High burden of private mutations due to explosive human population growth and purifying selection

BMC genomics, 2014, Vol.15 Suppl 4 (S4), p.S3-S3, Article S3

2014

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Contrasting X-Linked and Autosomal Diversity across 14 Human Populations

Human population differentiation is strongly correlated with local recombination rate

XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome

Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

Principal component analysis characterizes shared pathogenetics from genome-wide association studies

Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases

NRE: a tool for exploring neutral loci in the human genome

Gene-based testing of interactions in association studies of quantitative traits

The history of African gene flow into Southern Europeans, Levantines, and Jews

Accelerated genetic drift on chromosome X during the human dispersal out of Africa

Incomplete Lineage Sorting and Hybridization Statistics for Large-Scale Retroposon Insertion Data

Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits

Extracting replicable associations across multiple studies: Empirical Bayes algorithms for controlling the false discovery rate

Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation

Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations

Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels

Enhanced methods for local ancestry assignment in sequenced admixed individuals

Gene-Based Nonparametric Testing of Interactions Using Distance Correlation Coefficient in Case-Control Association Studies

Human dominant disease genes are enriched in paralogs originating from whole genome duplication

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry

Explosive genetic evidence for explosive human population growth

Historical pedigree reconstruction from extant populations using PArtitioning of RElatives (PREPARE)

Comments on "Human dominant disease genes are enriched in paralogs originating from whole genome duplication"

Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions

High burden of private mutations due to explosive human population growth and purifying selection

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