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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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Mutations in the gene encoding GlyT2 ( SLC6A5 ) define a presynaptic component of human startle disease

Nature genetics, 2006-07, Vol.38 (7), p.801-806

2006

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Nature genetics, 2019-01, Vol.51 (1), p.63-75

2019

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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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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Nature genetics, 2009-10, Vol.41 (10), p.1088-1093

2009

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Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Nature genetics, 2024-07, Vol.56 (7), p.1371-1376

2024

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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Nature genetics, 2011-05, Vol.43 (5), p.429-435

2011

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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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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Nature genetics, 2010-07, Vol.42 (7), p.579-589

2010

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Nature genetics, 2013-10, Vol.45 (10), p.1150-1159

2013

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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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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Nature genetics, 2013-03, Vol.45 (3), p.314-318

2013

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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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Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

Nature genetics, 2009-10, Vol.41 (10), p.1116-1121

2009

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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

Nature genetics, 2008-05, Vol.40 (5), p.638-645

2008

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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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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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Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

Nature genetics, 2020-02, Vol.52 (2), p.160-166

2020

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Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature genetics, 2024-06, Vol.56 (6), p.1090-1099

2024

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Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Nature genetics, 2021-02, Vol.53 (2), p.135-142

2021

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The amino acid transporter SLC7A5 is required for efficient growth of KRAS-mutant colorectal cancer

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

Mutations in the gene encoding GlyT2 ( SLC6A5 ) define a presynaptic component of human startle disease

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

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

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

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

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

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

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Multiple loci on 8q24 associated with prostate cancer susceptibility

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

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

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

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

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

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

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

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

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