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Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins

Nature genetics, 2015-01, Vol.47 (1), p.88-91

2015

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An atlas of genetic influences on osteoporosis in humans and mice

Nature genetics, 2019-02, Vol.51 (2), p.258-266

2019

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Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance

Nature genetics, 2016-10, Vol.48 (10), p.1131-1141

2016

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Positional cloning of Sorcs1 , a type 2 diabetes quantitative trait locus

Nature genetics, 2006-06, Vol.38 (6), p.688-693

2006

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The landscape of selection in 551 esophageal adenocarcinomas defines genomic biomarkers for the clinic

Nature genetics, 2019-03, Vol.51 (3), p.506-516

2019

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Nature genetics, 2011-04, Vol.43 (4), p.329-332

2011

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Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis

Nature genetics, 2017-10, Vol.49 (10), p.1468-1475

2017

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The genetic landscape of mutations in Burkitt lymphoma

Nature genetics, 2012-12, Vol.44 (12), p.1321-1325

2012

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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Nature genetics, 2012-07, Vol.44 (7), p.770-776

2012

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Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

Nature genetics, 2020-12, Vol.52 (12), p.1303-1313

2020

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A reference panel of 64,976 haplotypes for genotype imputation

Nature genetics, 2016-10, Vol.48 (10), p.1279-1283

2016

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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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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Nature genetics, 2013-09, Vol.45 (9), p.984-994

2013

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

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

2017

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The common marmoset genome provides insight into primate biology and evolution

Nature genetics, 2014-08, Vol.46 (8), p.850-857

2014

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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

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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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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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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

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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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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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Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins

An atlas of genetic influences on osteoporosis in humans and mice

Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance

Positional cloning of Sorcs1 , a type 2 diabetes quantitative trait locus

The landscape of selection in 551 esophageal adenocarcinomas defines genomic biomarkers for the clinic

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis

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

The genetic landscape of mutations in Burkitt lymphoma

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

A reference panel of 64,976 haplotypes for genotype imputation

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

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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

Multiple loci on 8q24 associated with prostate cancer susceptibility

Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis

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

The common marmoset genome provides insight into primate biology and evolution

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

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

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

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

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

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

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