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PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations

Bioinformatics, 2019-11, Vol.35 (22), p.4851-4853

2019

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PhenoScanner: a database of human genotype-phenotype associations

Bioinformatics (Oxford, England), 2016-10, Vol.32 (20), p.3207-3209

2016

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A robust and efficient method for Mendelian randomization with hundreds of genetic variants

Nature communications, 2020-01, Vol.11 (1), p.376-376, Article 376

2020

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A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits

Nature communications, 2021-02, Vol.12 (1), p.764-764, Article 764

2021

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The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

Cell, 2016-11, Vol.167 (5), p.1415-1429.e19

2016

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Semiparametric methods for estimation of a nonlinear exposure‐outcome relationship using instrumental variables with application to Mendelian randomization

Genetic epidemiology, 2017-05, Vol.41 (4), p.341-352

2017

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Coding and regulatory variants are associated with serum protein levels and disease

Nature communications, 2022-01, Vol.13 (1), p.481-11, Article 481

2022

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The EWAS Catalog: a database of epigenome-wide association studies

Wellcome open research, 2022, Vol.7, p.41

2022

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DNA methylation signatures of adolescent victimization: analysis of a longitudinal monozygotic twin sample

Epigenetics, 2021-11, Vol.16 (11), p.1169-1186

2021

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Associations of Blood Pressure in Pregnancy With Offspring Blood Pressure Trajectories During Childhood and Adolescence: Findings From a Prospective Study

Journal of the American Heart Association, 2015-05, Vol.4 (5), p.n/a

2015

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MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data

Wellcome open research, 2020, Vol.5, p.252-252

2020

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Genomic atlas of the human plasma proteome

Nature (London), 2018-06, Vol.558 (7708), p.73-79

2018

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Genetic data do not provide evidence that lower sclerostin is associated with increased risk of atherosclerosis: comment on the article by Zheng et al

Arthritis & rheumatology (Hoboken, N.J.), 2024-01

2024

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Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses

BMJ (Online), 2019-03, Vol.364, p.l1042

2019

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Sclerostin Downregulation Globally by Naturally Occurring Genetic Variants, or Locally in Atherosclerotic Plaques, Does Not Associate With Cardiovascular Events in Humans

Journal of bone and mineral research, 2021-07, Vol.36 (7), p.1326-1339

2021

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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

Nature genetics, 2016-10, Vol.48 (10), p.1151-1161

2016

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The Effect of Attention Deficit/Hyperactivity Disorder on Physical Health Outcomes: A 2-Sample Mendelian Randomization Study

American journal of epidemiology, 2021-06, Vol.190 (6), p.1047-1055

2021

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A robust mean and variance test with application to high-dimensional phenotypes

European journal of epidemiology, 2022-04, Vol.37 (4), p.377-387

2022

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The EWAS Catalog: a database of epigenome-wide association studies

Wellcome open research, 2022-01, Vol.7, p.41-41

2022

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A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.854-862

2017

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The impact of fatty acids biosynthesis on the risk of cardiovascular diseases in Europeans and East Asians: a Mendelian randomization study

Human molecular genetics, 2022-11, Vol.31 (23), p.4034-4054

2022

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Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses

Circulation (New York, N.Y.), 2022, Vol.146 (20), p.1507-1517

2022

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Longitudinal analysis strategies for modelling epigenetic trajectories

International journal of epidemiology, 2018-04, Vol.47 (2), p.516-525

2018

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PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations

PhenoScanner: a database of human genotype-phenotype associations

A robust and efficient method for Mendelian randomization with hundreds of genetic variants

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

Semiparametric methods for estimation of a nonlinear exposure‐outcome relationship using instrumental variables with application to Mendelian randomization

Coding and regulatory variants are associated with serum protein levels and disease

The EWAS Catalog: a database of epigenome-wide association studies

DNA methylation signatures of adolescent victimization: analysis of a longitudinal monozygotic twin sample

Associations of Blood Pressure in Pregnancy With Offspring Blood Pressure Trajectories During Childhood and Adolescence: Findings From a Prospective Study

MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data

Genomic atlas of the human plasma proteome

Genetic data do not provide evidence that lower sclerostin is associated with increased risk of atherosclerosis: comment on the article by Zheng et al

Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses

Association of LPA Variants With Risk of Coronary Disease and the Implications for Lipoprotein(a)-Lowering Therapies: A Mendelian Randomization Analysis

Sclerostin Downregulation Globally by Naturally Occurring Genetic Variants, or Locally in Atherosclerotic Plaques, Does Not Associate With Cardiovascular Events in Humans

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

The Effect of Attention Deficit/Hyperactivity Disorder on Physical Health Outcomes: A 2-Sample Mendelian Randomization Study

A robust mean and variance test with application to high-dimensional phenotypes

The EWAS Catalog: a database of epigenome-wide association studies

A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design

The impact of fatty acids biosynthesis on the risk of cardiovascular diseases in Europeans and East Asians: a Mendelian randomization study

Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses

Longitudinal analysis strategies for modelling epigenetic trajectories

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