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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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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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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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The DNA methylation landscape of advanced prostate cancer

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

2020

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

Nature genetics, 2022-05, Vol.54 (5), p.581-592

2022

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Integrated analyses highlight interactions between the three-dimensional genome and DNA, RNA and epigenomic alterations in metastatic prostate cancer

Nature genetics, 2024-07

2024

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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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Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

Nature genetics, 2022-11, Vol.54 (11), p.1640-1651

2022

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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 a locus at 7p15.2 associated with endometriosis

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

2011

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Defining the role of common variation in the genomic and biological architecture of adult human height

Nature genetics, 2014-11, Vol.46 (11), p.1173-1186

2014

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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

Nature genetics, 2019-01, Vol.51 (1), p.51-62

2019

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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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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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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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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Nature genetics, 2018-08, Vol.50 (8), p.1112-1121

2018

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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

Volltextzugriff (PDF)

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

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

2013

Volltextzugriff (PDF)

The Cancer Genome Atlas Pan-Cancer analysis project

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

2013

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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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Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

Nature genetics, 2018-05, Vol.50 (5), p.652-656

2018

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

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

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

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

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

The DNA methylation landscape of advanced prostate cancer

Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

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

Integrated analyses highlight interactions between the three-dimensional genome and DNA, RNA and epigenomic alterations in metastatic prostate cancer

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

Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

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 a locus at 7p15.2 associated with endometriosis

Defining the role of common variation in the genomic and biological architecture of adult human height

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

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

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

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

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

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

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

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

The Cancer Genome Atlas Pan-Cancer analysis project

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

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

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