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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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Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome

Journal of translational medicine, 2016-01, Vol.14 (18), p.19-19, Article 19

2016

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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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Human Population Differentiation Is Strongly Correlated with Local Recombination Rate: e1000886

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

2010

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Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity

Genome research, 2016-05, Vol.26 (5), p.579-587

2016

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Controlled analysis of neurocontrollers with informational lesioning

Philosophical transactions of the Royal Society of London. Series A: Mathematical, physical, and engineering sciences, 2003-10, Vol.361 (1811), p.2123-2144

2003

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Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia

Atherosclerosis, 2014-06, Vol.234 (2), p.249-253

2014

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The genetic history of Cochin Jews from India

Human genetics, 2016-10, Vol.135 (10), p.1127-1143

2016

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Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms

Journal of translational medicine, 2016-12, Vol.14 (1), p.342-342, Article 342

2016

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Selection for translation efficiency on synonymous polymorphisms in recent human evolution

Genome biology and evolution, 2011-01, Vol.3, p.749-761

2011

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Fair localization of function via multi-lesion analysis

Neuroinformatics (Totowa, N.J.), 2004, Vol.2 (2), p.163-168

2004

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Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus

Immunology letters, 2017-01, Vol.181, p.58-62

2017

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Biological knowledge-driven analysis of epistasis in human GWAS with application to lipid traits

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1253, p.35

2015

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Sex-Averaged Recombination and Mutation Rates on the X Chromosome: A Comment on Labuda et al

American journal of human genetics, 2010-06, Vol.86 (6), p.978-980

2010

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A 22 bp FADS2 Insertion‐Deletion (Indel) Polymorphism Influences Arachidonic Acid Status

The FASEB journal, 2016-04, Vol.30 (S1)

2016

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Combining Evidence of Natural Selection with Association Analysis Increases Power to Detect Malaria-Resistance Variants

American journal of human genetics, 2007-08, Vol.81 (2), p.234-242

2007

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Association of rs2294020 in the X-linked CCDC22 with susceptibility to autoimmune diseases with focus on systemic lupus erythematosus

Immunology letters, 2016-11, Vol.181, p.58-62

2016

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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

Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome

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

Human Population Differentiation Is Strongly Correlated with Local Recombination Rate: e1000886

Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity

Controlled analysis of neurocontrollers with informational lesioning

Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia

The genetic history of Cochin Jews from India

Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms

Population Genetic Inference from Personal Genome Data: Impact of Ancestry and Admixture on Human Genomic Variation

Selection for translation efficiency on synonymous polymorphisms in recent human evolution

Fair localization of function via multi-lesion analysis

Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus

Biological knowledge-driven analysis of epistasis in human GWAS with application to lipid traits

Sex-Averaged Recombination and Mutation Rates on the X Chromosome: A Comment on Labuda et al

A 22 bp FADS2 Insertion‐Deletion (Indel) Polymorphism Influences Arachidonic Acid Status

Combining Evidence of Natural Selection with Association Analysis Increases Power to Detect Malaria-Resistance Variants

Association of rs2294020 in the X-linked CCDC22 with susceptibility to autoimmune diseases with focus on systemic lupus erythematosus

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