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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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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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Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

Nature communications, 2015-08, Vol.6 (1), p.7502-7502, Article 7502

2015

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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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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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Long COVID burden and risk factors in 10 UK longitudinal studies and electronic health records

Nature communications, 2022-06, Vol.13 (1), p.3528-3528, Article 3528

2022

Volltextzugriff (PDF)

Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

Nature medicine, 2021-03, Vol.27 (3), p.546-559

2021

Volltextzugriff (PDF)

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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Intensity and timing of physical activity in relation to postmenopausal breast cancer risk: the prospective NIH-AARP diet and health study

BMC cancer, 2009-10, Vol.9 (1), p.349-349, Article 349

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2013

Volltextzugriff (PDF)

Cerebral small vessel disease genomics and its implications across the lifespan

Nature communications, 2020-12, Vol.11 (1), p.6285-6285, Article 6285

2020

Volltextzugriff (PDF)

Genome-wide association study identifies five new schizophrenia loci

Nature genetics, 2011-10, Vol.43 (10), p.969-976

2011

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Recurrent MET fusion genes represent a drug target in pediatric glioblastoma

Nature medicine, 2016-11, Vol.22 (11), p.1314-1320

2016

Volltextzugriff (PDF)

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Nature genetics, 2012-12, Vol.44 (12), p.1336-1340

2012

Volltextzugriff (PDF)

PPARβ/δ promotes HRAS-induced senescence and tumor suppression by potentiating p-ERK and repressing p-AKT signaling

Oncogene, 2014-11, Vol.33 (46), p.5348-5359

2014

Volltextzugriff (PDF)

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

Nature genetics, 2011-06, Vol.43 (6), p.561-564

2011

Volltextzugriff (PDF)

A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank

Nature communications, 2020-05, Vol.11 (1), p.2301-16, Article 2301

2020

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1 – 25 von 37

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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

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

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

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

The effect of LRRK2 loss-of-function variants in humans

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

Long COVID burden and risk factors in 10 UK longitudinal studies and electronic health records

Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

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

Intensity and timing of physical activity in relation to postmenopausal breast cancer risk: the prospective NIH-AARP diet and health study

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

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

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

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

Cerebral small vessel disease genomics and its implications across the lifespan

Genome-wide association study identifies five new schizophrenia loci

Recurrent MET fusion genes represent a drug target in pediatric glioblastoma

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

PPARβ/δ promotes HRAS-induced senescence and tumor suppression by potentiating p-ERK and repressing p-AKT signaling

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank

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