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Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants

Science (American Association for the Advancement of Science), 2012-05, Vol.336 (6082), p.740-743

2012

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Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (29), p.10654-10659

2014

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Host genetic variation impacts microbiome composition across human body sites

Genome Biology, 2015-09, Vol.16 (1), p.191, Article 191

2015

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Crowdsourced genealogies and genomes

Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6385), p.153-154

2018

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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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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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Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations

Nature communications, 2019-09, Vol.10 (1), p.4141-15, Article 4141

2019

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Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations

Genome research, 2016-02, Vol.26 (2), p.151-162

2016

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Neutral genomic regions refine models of recent rapid human population growth

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (2), p.757-762

2014

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Reply to Just et al.: Mitochondrial DNA heteroplasmy could be reliably detected with massively parallel sequencing technologies

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (43), p.E4548-E4550

2014

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Inference of Super-exponential Human Population Growth via Efficient Computation of the Site Frequency Spectrum for Generalized Models

Genetics (Austin), 2016-01, Vol.202 (1), p.235-245

2016

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Interaction between SNPs in the RXRA and near ANGPTL3 gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia

Journal of lipid research, 2012-11, Vol.53 (11), p.2425-2428

2012

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Crowdsourced genealogies and genomes: Genealogical study provides insight into history and life span and heralds crowdsourced genetic research

Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6385), p.153-154

2018

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Fair Attribution of Functional Contribution in Artificial and Biological Networks

Neural computation, 2004-09, Vol.16 (9), p.1887-1915

2004

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Principal Component Analysis Characterizes Shared Pathogenetics from Genome-Wide Association Studies: e1003820

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

2014

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Regional dietary adaptation of FADS genes in humans: molecular mechanism and functional consequences

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect

Genetics (Austin), 2013-11, Vol.195 (3), p.969-978

2013

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Genome-wide inference of natural selection on human transcription factor binding sites

Nature genetics, 2013-07, Vol.45 (7), p.723-729

2013

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Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing

Nature genetics, 2011-08, Vol.43 (8), p.741-743

2011

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Dietary adaptation of FADS genes in Europe varied across time and geography

Nature ecology & evolution, 2017-05, Vol.1 (7), Article 0167

2017

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Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes

Molecular biology and evolution, 2016-02, Vol.33 (2), p.384-393

2016

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The utility of ancient human DNA for improving allele age estimates, with implications for demographic models and tests of natural selection

Journal of human evolution, 2015-02, Vol.79, p.64-72

2015

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Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid

Molecular biology and evolution, 2016-07, Vol.33 (7), p.1726-1739

2016

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Can a sex-biased human demography account for the reduced effective population size of chromosome X in non-Africans?

Molecular biology and evolution, 2010-10, Vol.27 (10), p.2312-2321

2010

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Causal localization of neural function: the Shapley value method

Neurocomputing (Amsterdam), 2004-06, Vol.58, p.215-222

2004

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Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants

Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

Host genetic variation impacts microbiome composition across human body sites

Crowdsourced genealogies and genomes

Contrasting X-Linked and Autosomal Diversity across 14 Human Populations

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

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations

Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations

Neutral genomic regions refine models of recent rapid human population growth

Reply to Just et al.: Mitochondrial DNA heteroplasmy could be reliably detected with massively parallel sequencing technologies

Inference of Super-exponential Human Population Growth via Efficient Computation of the Site Frequency Spectrum for Generalized Models

Interaction between SNPs in the RXRA and near ANGPTL3 gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia

Crowdsourced genealogies and genomes: Genealogical study provides insight into history and life span and heralds crowdsourced genetic research

Fair Attribution of Functional Contribution in Artificial and Biological Networks

Principal Component Analysis Characterizes Shared Pathogenetics from Genome-Wide Association Studies: e1003820

Regional dietary adaptation of FADS genes in humans: molecular mechanism and functional consequences

Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect

Genome-wide inference of natural selection on human transcription factor binding sites

Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing

Dietary adaptation of FADS genes in Europe varied across time and geography

Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes

The utility of ancient human DNA for improving allele age estimates, with implications for demographic models and tests of natural selection

Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid

Can a sex-biased human demography account for the reduced effective population size of chromosome X in non-Africans?

Causal localization of neural function: the Shapley value method

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