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An atlas of genetic associations in UK Biobank

Nature genetics, 2018-11, Vol.50 (11), p.1593-1599

2018

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Mendelian randomization study of whole blood viscosity and cardiovascular diseases

PloS one, 2024-04, Vol.19 (4), p.e0294095-e0294095

2024

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The heritability of human disease: estimation, uses and abuses

Nature reviews. Genetics, 2013-02, Vol.14 (2), p.139-149

2013

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Evidence for sex-specific genetic architectures across a spectrum of human complex traits

Genome Biology, 2016-07, Vol.17 (1), p.166-166, Article 166

2016

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Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability

Nature communications, 2018-12, Vol.9 (1), p.5271-10, Article 5271

2018

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Indirect assortative mating for human disease and longevity

Heredity, 2019-08, Vol.123 (2), p.106-116

2019

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Plasma Vitamin D Concentration Influences Survival Outcome After a Diagnosis of Colorectal Cancer

Journal of clinical oncology, 2014-08, Vol.32 (23), p.2430-2439

2014

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Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Nature communications, 2019-03, Vol.10 (1), p.1383-1383, Article 1383

2019

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Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

Gut, 2010-12, Vol.59 (12), p.1670-1679

2010

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Functional annotation of the cattle genome through systematic discovery and characterization of chromatin states and butyrate-induced variations

BMC biology, 2019-08, Vol.17 (1), p.68-16, Article 68

2019

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Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human

BMC biology, 2020-07, Vol.18 (1), p.80-80, Article 80

2020

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Genetic contributions to stability and change in intelligence from childhood to old age

Nature (London), 2012-02, Vol.482 (7384), p.212-215

2012

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Evidence of horizontal indirect genetic effects in humans

Nature human behaviour, 2021-03, Vol.5 (3), p.399-406

2021

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Recent human effective population size estimated from linkage disequilibrium

Genome Research, 2007-04, Vol.17 (4), p.520-526

2007

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Identification and Survival of Carriers of Mutations in DNA Mismatch-Repair Genes in Colon Cancer

The New England journal of medicine, 2006-06, Vol.354 (26), p.2751-2763

2006

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Comparative transcriptome in large-scale human and cattle populations

Genome Biology, 2022-08, Vol.23 (1), p.176-24, Article 176

2022

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Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle

Cell genomics, 2023-10, Vol.3 (10), p.100385-100385, Article 100385

2023

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Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

Nature genetics, 2010-06, Vol.42 (6), p.520-524

2010

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The association of dietary intake of purine-rich vegetables, sugar-sweetened beverages and dairy with plasma urate, in a cross-sectional study

PloS one, 2012-06, Vol.7 (6), p.e38123

2012

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Dietary Flavonoids and the Risk of Colorectal Cancer

Cancer epidemiology, biomarkers & prevention, 2007-04, Vol.16 (4), p.684-693

2007

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Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

PLoS genetics, 2020-07, Vol.16 (7), p.e1008785-e1008785

2020

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Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach

PloS one, 2016-12, Vol.11 (12), p.e0166755-e0166755

2016

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Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Nature communications, 2019-05, Vol.10 (1), p.2069-2069, Article 2069

2019

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Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects

American journal of human genetics, 2005-07, Vol.77 (1), p.112-119

2005

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An atlas of genetic associations in UK Biobank

Mendelian randomization study of whole blood viscosity and cardiovascular diseases

The heritability of human disease: estimation, uses and abuses

Evidence for sex-specific genetic architectures across a spectrum of human complex traits

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability

Indirect assortative mating for human disease and longevity

Plasma Vitamin D Concentration Influences Survival Outcome After a Diagnosis of Colorectal Cancer

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Effect of aspirin and NSAIDs on risk and survival from colorectal cancer

Functional annotation of the cattle genome through systematic discovery and characterization of chromatin states and butyrate-induced variations

Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human

Genetic contributions to stability and change in intelligence from childhood to old age

Evidence of horizontal indirect genetic effects in humans

Recent human effective population size estimated from linkage disequilibrium

Identification and Survival of Carriers of Mutations in DNA Mismatch-Repair Genes in Colon Cancer

Comparative transcriptome in large-scale human and cattle populations

Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

The association of dietary intake of purine-rich vegetables, sugar-sweetened beverages and dairy with plasma urate, in a cross-sectional study

Dietary Flavonoids and the Risk of Colorectal Cancer

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Common genetic variants at the CRAC1 ( HMPS ) locus on chromosome 15q13.3 influence colorectal cancer risk

Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects

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