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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 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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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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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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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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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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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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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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Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Nature genetics, 2018-04, Vol.50 (4), p.621-629

2018

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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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Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature genetics, 2015-11, Vol.47 (11), p.1228-1235

2015

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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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High-throughput inference of pairwise coalescence times identifies signals of selection and enriched disease heritability

Nature genetics, 2018-09, Vol.50 (9), p.1311-1317

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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Abundant contribution of short tandem repeats to gene expression variation in humans

Nature genetics, 2016-01, Vol.48 (1), p.22-29

2016

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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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Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

Nature genetics, 2018-11, Vol.50 (11), p.1600-1607

2018

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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Nature genetics, 2018-04, Vol.50 (4), p.538-548

2018

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Progress and promise in understanding the genetic basis of common diseases

Proceedings of the Royal Society. B, Biological sciences, 2015-12, Vol.282 (1821), p.20151684-20151684

2015

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Distinguishing genetic correlation from causation across 52 diseases and complex traits

Reference-based phasing using the Haplotype Reference Consortium panel

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

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

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

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

Population structure and eigenanalysis

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

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

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

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Pitfalls of predicting complex traits from SNPs

Partitioning heritability by functional annotation using genome-wide association summary statistics

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

High-throughput inference of pairwise coalescence times identifies signals of selection and enriched disease heritability

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

Abundant contribution of short tandem repeats to gene expression variation in humans

Dissecting the genetics of complex traits using summary association statistics

Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Progress and promise in understanding the genetic basis of common diseases

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