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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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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Nature genetics, 2018-10, Vol.50 (10), p.1412-1425

2018

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Nature genetics, 2018-11, Vol.50 (11), p.1505-1513

2018

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Timing, rates and spectra of human germline mutation

Nature genetics, 2016-02, Vol.48 (2), p.126-133

2016

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The trans-ancestral genomic architecture of glycemic traits

Nature genetics, 2021-06, Vol.53 (6), p.840-860

2021

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Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4

Nature genetics, 1998-08, Vol.19 (4), p.379-383

1998

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Nature genetics, 2011-04, Vol.43 (4), p.329-332

2011

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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Nature genetics, 2015-04, Vol.47 (4), p.373-380

2015

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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature genetics, 2021-09, Vol.53 (9), p.1300-1310

2021

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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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Exome-wide association study of plasma lipids in >300,000 individuals

Nature genetics, 2017-12, Vol.49 (12), p.1758-1766

2017

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Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Nature genetics, 2012-10, Vol.44 (10), p.1131-1136

2012

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Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Nature genetics, 2011-10, Vol.43 (10), p.1005-1011

2011

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Histone H3 lysine 9 methylation is an epigenetic imprint of facultative heterochromatin

Nature genetics, 2002-01, Vol.30 (1), p.77-80

2002

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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease

Nature genetics, 2021-09, Vol.53 (9), p.1276-1282

2021

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Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Nature genetics, 2010-05, Vol.42 (5), p.441-447

2010

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Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

Nature genetics, 2012-08, Vol.44 (8), p.904-909

2012

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Nature genetics, 2017-06, Vol.49 (6), p.946-952

2017

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Nature genetics, 2014-03, Vol.46 (3), p.234-244

2014

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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Nature genetics, 2012-09, Vol.44 (9), p.981-990

2012

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Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Nature genetics, 2015-12, Vol.47 (12), p.1449-1456

2015

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

A functional genomics predictive network model identifies regulators of inflammatory bowel disease

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

Timing, rates and spectra of human germline mutation

Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population

The trans-ancestral genomic architecture of glycemic traits

Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

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

Exome-wide association study of plasma lipids in >300,000 individuals

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Histone H3 lysine 9 methylation is an epigenetic imprint of facultative heterochromatin

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

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