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Inferring protein 3D structure from deep mutation scans

Nature genetics, 2019-07, Vol.51 (7), p.1170-1176

2019

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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

Nature genetics, 2009-07, Vol.41 (7), p.824-828

2009

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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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Comparative genomics of the major parasitic worms

Nature genetics, 2019-01, Vol.51 (1), p.163-174

2019

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Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

Nature genetics, 2020-07, Vol.52 (7), p.680-691

2020

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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Nature genetics, 2014-02, Vol.46 (2), p.107-115

2014

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Genome-wide association study identifies eight loci associated with blood pressure

Nature genetics, 2009-06, Vol.41 (6), p.666-676

2009

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Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease

Nature genetics, 2017-12, Vol.49 (12), p.1664-1670

2017

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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Nature genetics, 2017-03, Vol.49 (3), p.403-415

2017

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Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution

Nature genetics, 2023-12, Vol.55 (12), p.2255-2268

2023

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Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature genetics, 2023-02, Vol.55 (2), p.198-208

2023

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Genome-wide and fine-resolution association analysis of malaria in West Africa

Nature genetics, 2009-06, Vol.41 (6), p.657-665

2009

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Common variants near MC4R are associated with fat mass, weight and risk of obesity

Nature genetics, 2008-06, Vol.40 (6), p.768-775

2008

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The Genotype-Tissue Expression (GTEx) project

Nature genetics, 2013-06, Vol.45 (6), p.580-585

2013

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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature genetics, 2020-12, Vol.52 (12), p.1314-1332

2020

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Nature genetics, 2015-12, Vol.47 (12), p.1415-1425

2015

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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Nature genetics, 2012-08, Vol.44 (8), p.934-940

2012

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A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature genetics, 2012-06, Vol.44 (6), p.659-669

2012

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Nature genetics, 2011-10, Vol.43 (10), p.977-983

2011

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Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer

Nature genetics, 2022-06, Vol.54 (6), p.850-860

2022

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Inferring protein 3D structure from deep mutation scans

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

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

Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas

Comparative genomics of the major parasitic worms

Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Genome-wide association study identifies eight loci associated with blood pressure

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Genome-wide and fine-resolution association analysis of malaria in West Africa

Common variants near MC4R are associated with fat mass, weight and risk of obesity

The Genotype-Tissue Expression (GTEx) project

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Bayesian refinement of association signals for 14 loci in 3 common diseases

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer

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