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Comparative genomics of the major parasitic worms

Nature genetics, 2019-01, Vol.51 (1), p.163-174

2019

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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature genetics, 2021-02, Vol.53 (2), p.128-134

2021

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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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Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

Nature genetics, 2015-04, Vol.47 (4), p.367-372

2015

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature genetics, 2022-09, Vol.54 (9), p.1320-1331

2022

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Nature genetics, 2015-04, Vol.47 (4), p.387-392

2015

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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 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

Volltextzugriff (PDF)

Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease

Nature genetics, 2017-12, Vol.49 (12), p.1664-1670

2017

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature genetics, 2023-01, Vol.55 (1), p.154-164

2023

Volltextzugriff (PDF)

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

Nature genetics, 2009-07, Vol.41 (7), p.824-828

2009

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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

Nature genetics, 2013-07, Vol.45 (7), p.730-738

2013

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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Nature genetics, 2015-03, Vol.47 (3), p.257-262

2015

Volltextzugriff (PDF)

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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Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma

Nature genetics, 2015-09, Vol.47 (9), p.1038-1046

2015

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Variation in genome-wide mutation rates within and between human families

Nature genetics, 2011-07, Vol.43 (7), p.712-714

2011

Volltextzugriff (PDF)

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Nature genetics, 2012-12, Vol.44 (12), p.1349-1354

2012

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Comparative genomics of the major parasitic worms

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

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

Germline hypomorphic CARD11 mutations in severe atopic disease

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

Bayesian refinement of association signals for 14 loci in 3 common diseases

Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

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

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

Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease

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

Multiple loci on 8q24 associated with prostate cancer susceptibility

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

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

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

Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma

Variation in genome-wide mutation rates within and between human families

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

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