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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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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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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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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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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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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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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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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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Integrating common and rare genetic variation in diverse human populations

Nature (London), 2010-09, Vol.467 (7311), p.52-58

2010

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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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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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Causal localization of neural function: the Shapley value method

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

2004

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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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The genetic history of Cochin Jews from India

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

2016

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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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Fair localization of function via multi-lesion analysis

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

2004

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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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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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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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Contrasting human X-linked and autosomal variation in population-scale whole genome sequencing

Nature genetics, 2011-07, Vol.43 (8), p.741-743

2011

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Axiomatic scalable neurocontroller analysis via the Shapley value

Artificial life, 2006-07, Vol.12 (3), p.333-352

2006

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Neurocontroller analysis via evolutionary network minimization

Artificial life, 2006-07, Vol.12 (3), p.435-448

2006

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Neural processing of counting in evolved spiking and McCulloch-Pitts agents

Artificial life, 2006, Vol.12 (1), p.1-16

2006

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Spikes that count: rethinking spikiness in neurally embedded systems

Neurocomputing (Amsterdam), 2004-06, Vol.58, p.303-311

2004

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Host genetic variation impacts microbiome composition across human body sites

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

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

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

Explosive genetic evidence for explosive human population growth

Fair Attribution of Functional Contribution in Artificial and Biological Networks

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

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

Integrating common and rare genetic variation in diverse human populations

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

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

Causal localization of neural function: the Shapley value method

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

The genetic history of Cochin Jews from India

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

Fair localization of function via multi-lesion analysis

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

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

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

Contrasting human X-linked and autosomal variation in population-scale whole genome sequencing

Axiomatic scalable neurocontroller analysis via the Shapley value

Neurocontroller analysis via evolutionary network minimization

Neural processing of counting in evolved spiking and McCulloch-Pitts agents

Spikes that count: rethinking spikiness in neurally embedded systems

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