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Dissecting the genetics of complex traits using summary association statistics

Nature reviews. Genetics, 2017-02, Vol.18 (2), p.117-127

2017

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Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

PLoS genetics, 2013-05, Vol.9 (5), p.e1003520-e1003520

2013

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Integrating functional data to prioritize causal variants in statistical fine-mapping studies

PLoS genetics, 2014-10, Vol.10 (10), p.e1004722-e1004722

2014

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Population structure and eigenanalysis

PLoS genetics, 2006-12, Vol.2 (12), p.e190-e190

2006

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Adjusting for Heritable Covariates Can Bias Effect Estimates in Genome-Wide Association Studies

American journal of human genetics, 2015-02, Vol.96 (2), p.329-339

2015

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Distinguishing genetic correlation from causation across 52 diseases and complex traits

Nature genetics, 2018-12, Vol.50 (12), p.1728-1734

2018

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Reference-based phasing using the Haplotype Reference Consortium panel

Nature genetics, 2016-11, Vol.48 (11), p.1443-1448

2016

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Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia

American journal of human genetics, 2016-03, Vol.98 (3), p.456-472

2016

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Fast and accurate long-range phasing in a UK Biobank cohort

Nature genetics, 2016-07, Vol.48 (7), p.811-816

2016

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Leveraging Polygenic Functional Enrichment to Improve GWAS Power

American journal of human genetics, 2019-01, Vol.104 (1), p.65-75

2019

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Estimating and interpreting FST: the impact of rare variants

Genome research, 2013-09, Vol.23 (9), p.1514

2013

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Advantages and pitfalls in the application of mixed-model association methods

Nature genetics, 2014-02, Vol.46 (2), p.100-106

2014

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Extreme Polygenicity of Complex Traits Is Explained by Negative Selection

American journal of human genetics, 2019-09, Vol.105 (3), p.456-476

2019

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New approaches to population stratification in genome-wide association studies

Nature reviews. Genetics, 2010-07, Vol.11 (7), p.459-463

2010

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Mixed-model association for biobank-scale datasets

Nature genetics, 2018-07, Vol.50 (7), p.906-908

2018

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Reconstructing Indian population history

Nature, 2009-09, Vol.461 (7263), p.489-494

2009

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Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS

Nature genetics, 2021-04, Vol.53 (4), p.445-454

2021

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Sensitive detection of chromosomal segments of distinct ancestry in admixed populations

PLoS genetics, 2009-06, Vol.5 (6), p.e1000519-e1000519

2009

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Quantifying genetic effects on disease mediated by assayed gene expression levels

Nature genetics, 2020-06, Vol.52 (6), p.626-633

2020

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Population-specific causal disease effect sizes in functionally important regions impacted by selection

Nature communications, 2021-02, Vol.12 (1), p.1098-15, Article 1098

2021

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Functionally informed fine-mapping and polygenic localization of complex trait heritability

Nature genetics, 2020-12, Vol.52 (12), p.1355-1363

2020

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Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements

Nature genetics, 2020-12, Vol.52 (12), p.1346-1354

2020

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Quantitative analysis of population-scale family trees with millions of relatives

Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6385), p.171-175

2018

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Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection

Nature communications, 2019-02, Vol.10 (1), p.790-790, Article 790

2019

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Pitfalls of predicting complex traits from SNPs

Nature reviews. Genetics, 2013-07, Vol.14 (7), p.507-515

2013

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Dissecting the genetics of complex traits using summary association statistics

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

Population structure and eigenanalysis

Adjusting for Heritable Covariates Can Bias Effect Estimates in Genome-Wide Association Studies

Distinguishing genetic correlation from causation across 52 diseases and complex traits

Reference-based phasing using the Haplotype Reference Consortium panel

Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia

Fast and accurate long-range phasing in a UK Biobank cohort

Leveraging Polygenic Functional Enrichment to Improve GWAS Power

Estimating and interpreting FST: the impact of rare variants

Advantages and pitfalls in the application of mixed-model association methods

Extreme Polygenicity of Complex Traits Is Explained by Negative Selection

New approaches to population stratification in genome-wide association studies

Mixed-model association for biobank-scale datasets

Reconstructing Indian population history

Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS

Sensitive detection of chromosomal segments of distinct ancestry in admixed populations

Quantifying genetic effects on disease mediated by assayed gene expression levels

Population-specific causal disease effect sizes in functionally important regions impacted by selection

Functionally informed fine-mapping and polygenic localization of complex trait heritability

Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements

Quantitative analysis of population-scale family trees with millions of relatives

Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection

Pitfalls of predicting complex traits from SNPs

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