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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Nature genetics, 2013-11, Vol.45 (11), p.1353-1360

2013

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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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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature genetics, 2022-03, Vol.54 (3), p.263-273

2022

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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature genetics, 2019-02, Vol.51 (2), p.237-244

2019

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Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

Nature genetics, 2023-03, Vol.55 (3), p.520-520

2023

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Bi-allelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 over-activity and disordered cortical neuronal migration

Nature genetics, 2018-07, Vol.50 (8), p.1093-1101

2018

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Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Nature genetics, 2018-08, Vol.50 (8), p.1093-1101

2018

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The Cancer Genome Atlas Pan-Cancer analysis project

Nature genetics, 2013-10, Vol.45 (10), p.1113-1120

2013

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Common SNPs explain a large proportion of the heritability for human height

Nature genetics, 2010-07, Vol.42 (7), p.565-569

2010

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Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

Nature genetics, 2012-10, Vol.44 (10), p.1147-1151

2012

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Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

Nature genetics, 2009-11, Vol.41 (11), p.1173-1175

2009

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Nature genetics, 2017-11, Vol.49 (11), p.1593-1601

2017

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The DNA methylation landscape of advanced prostate cancer

Nature genetics, 2020-08, Vol.52 (8), p.778-789

2020

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DNA methylation landscapes in advanced prostate cancer

Nature genetics, 2020-07, Vol.52 (8), p.778-789

2020

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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Nature genetics, 2020-09, Vol.52 (9), p.969-983

2020

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Genome-wide association meta-analysis identifies new endometriosis risk loci

Nature genetics, 2012-12, Vol.44 (12), p.1355-1359

2012

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Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

Nature genetics, 2011-01, Vol.43 (1), p.51-54

2011

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Genome-wide association study identifies a locus at 7pl5.2 associated with endometriosis

Nature genetics, 2011-01, Vol.43 (1), p.51

2011

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Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

Nature genetics, 2011-12, Vol.43 (12), p.1241-1246

2011

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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

Nature genetics, 2021-05, Vol.53 (6), p.817-829

2021

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An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

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

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

Bi-allelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 over-activity and disordered cortical neuronal migration

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

The Cancer Genome Atlas Pan-Cancer analysis project

Common SNPs explain a large proportion of the heritability for human height

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

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

The DNA methylation landscape of advanced prostate cancer

DNA methylation landscapes in advanced prostate cancer

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Exome array analysis identifies novel loci and low-frequency variants for insulin processing and secretion

Genome-wide association meta-analysis identifies new endometriosis risk loci

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

Genome-wide association study identifies a locus at 7pl5.2 associated with endometriosis

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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