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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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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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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

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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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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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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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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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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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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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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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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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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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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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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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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Quantitative analysis of genetic and neuronal multi-perturbation experiments

PLoS computational biology, 2005-11, Vol.1 (6), p.e64

2005

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

Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals

Crowdsourced genealogies and genomes

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

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

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

Neutral genomic regions refine models of recent rapid human population growth

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

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

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

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

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

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

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

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

Quantitative analysis of genetic and neuronal multi-perturbation experiments

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

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