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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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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Nature genetics, 2017-02, Vol.49 (2), p.223-237

2017

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Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis

Nature genetics, 2014-08, Vol.46 (8), p.837-843

2014

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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Nature genetics, 2012-12, Vol.44 (12), p.1341-1348

2012

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Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Nature genetics, 2012-09, Vol.44 (9), p.991-1005

2012

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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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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Nature genetics, 2018-03, Vol.50 (3), p.381-389

2018

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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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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Nature genetics, 2018-04, Vol.50 (4), p.524-537

2018

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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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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Nature genetics, 2017-06, Vol.49 (6), p.834-841

2017

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Nature genetics, 2007-07, Vol.39 (7), p.882-888

2007

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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Nature genetics, 2012-07, Vol.44 (7), p.770-776

2012

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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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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Nature genetics, 2018-01, Vol.50 (1), p.26-41

2018

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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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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

Nature genetics, 2012-01, Vol.44 (1), p.67-72

2012

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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Nature genetics, 2018-06, Vol.50 (6), p.834-848

2018

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Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

Nature genetics, 2021-01, Vol.53 (1), p.86-99

2021

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Identification of seven loci affecting mean telomere length and their association with disease

Nature genetics, 2013-04, Vol.45 (4), p.422-427

2013

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Nature genetics, 2013-09, Vol.45 (9), p.984-994

2013

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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Nature genetics, 2022-09, Vol.54 (9), p.1332-1344

2022

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Discovery of 42 genome-wide significant loci associated with dyslexia

Nature genetics, 2022-11, Vol.54 (11), p.1621-1629

2022

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

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

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

Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

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

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

The trans-ancestral genomic architecture of glycemic traits

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

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

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

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

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

Identification of seven loci affecting mean telomere length and their association with disease

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Discovery of 42 genome-wide significant loci associated with dyslexia

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