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Fast, sensitive and accurate integration of single-cell data with Harmony

Nature methods, 2019-12, Vol.16 (12), p.1289-1296

2019

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Monogenic and polygenic inheritance become instruments for clonal selection

Nature (London), 2020-08, Vol.584 (7819), p.136-141

2020

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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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Reference-based phasing using the Haplotype Reference Consortium panel

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

2016

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Inferring admixture histories of human populations using linkage disequilibrium

Genetics (Austin), 2013-04, Vol.193 (4), p.1233-1254

2013

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A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases

Nature genetics, 2018-06, Vol.50 (6), p.857-864

2018

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Chromosomal alterations among age-related haematopoietic clones in Japan

Nature (London), 2020-08, Vol.584 (7819), p.130-135

2020

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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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Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

Science (American Association for the Advancement of Science), 2021-09, Vol.373 (6562), p.1499-1505

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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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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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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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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Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes

Nature communications, 2019-02, Vol.10 (1), p.569-11, Article 569

2019

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Ancient west Eurasian ancestry in southern and eastern Africa

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (7), p.2632-2637

2014

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Nature genetics, 2015-12, Vol.47 (12), p.1385-1392

2015

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Estimating cross‐population genetic correlations of causal effect sizes

Genetic epidemiology, 2019-03, Vol.43 (2), p.180-188

2019

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Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits

Nature genetics, 2018-07, Vol.50 (7), p.1041-1047

2018

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Reconstructing Austronesian population history in Island Southeast Asia

Nature communications, 2014-08, Vol.5 (1), p.4689-4689, Article 4689

2014

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GIGYF1 loss of function is associated with clonal mosaicism and adverse metabolic health

Nature communications, 2021-07, Vol.12 (1), p.4178-4178, Article 4178

2021

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A Robust Example of Collider Bias in a Genetic Association Study

American journal of human genetics, 2016-02, Vol.98 (2), p.392-393

2016

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GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation

Nature communications, 2019-10, Vol.10 (1), p.4719-10, Article 4719

2019

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Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

Nature communications, 2021-10, Vol.12 (1), p.6052-6052, Article 6052

2021

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Physical and neurobehavioral determinants of reproductive onset and success

Nature genetics, 2016-06, Vol.48 (6), p.617-623

2016

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Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes

PLoS genetics, 2020-10, Vol.16 (10), p.e1009078-e1009078

2020

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Fast, sensitive and accurate integration of single-cell data with Harmony

Monogenic and polygenic inheritance become instruments for clonal selection

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

Reference-based phasing using the Haplotype Reference Consortium panel

Inferring admixture histories of human populations using linkage disequilibrium

A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases

Chromosomal alterations among age-related haematopoietic clones in Japan

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

Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

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

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

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

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

Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes

Ancient west Eurasian ancestry in southern and eastern Africa

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Estimating cross‐population genetic correlations of causal effect sizes

Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits

Reconstructing Austronesian population history in Island Southeast Asia

GIGYF1 loss of function is associated with clonal mosaicism and adverse metabolic health

A Robust Example of Collider Bias in a Genetic Association Study

GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation

Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

Physical and neurobehavioral determinants of reproductive onset and success

Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes

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