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METAL: fast and efficient meta-analysis of genomewide association scans

Bioinformatics, 2010-09, Vol.26 (17), p.2190-2191

2010

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Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2022-08, Vol.146 (8), p.e93-e118

2022

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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

Nature genetics, 2018-09, Vol.50 (9), p.1335-1341

2018

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Genetic epidemiology, 2010-12, Vol.34 (8), p.816-834

2010

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Unravelling the genetic architecture of human complex traits through whole genome sequencing

Nature communications, 2023-06, Vol.14 (1), p.3520-3520, Article 3520

2023

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Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

Nature communications, 2020-10, Vol.11 (1), p.5404-12, Article 5404

2020

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LocusZoom: regional visualization of genome-wide association scan results

Bioinformatics, 2010-09, Vol.26 (18), p.2336-2337

2010

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Exploring and visualizing large-scale genetic associations by using PheWeb

Nature genetics, 2020-06, Vol.52 (6), p.550-552

2020

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Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Nature communications, 2021-07, Vol.12 (1), p.4350-4350, Article 4350

2021

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Genotype imputation

Annual review of genomics and human genetics, 2009-01, Vol.10 (1), p.387-406

2009

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Causal relationships between NAFLD, T2D and obesity have implications for disease subphenotyping

Journal of hepatology, 2020-08, Vol.73 (2), p.263-276

2020

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Electronic health records: the next wave of complex disease genetics

Human molecular genetics, 2018-05, Vol.27 (R1), p.R14-R21

2018

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The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities

Statistics in medicine, 2020-03, Vol.39 (6), p.773-800

2020

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Exome sequencing and characterization of 49,960 individuals in the UK Biobank

Nature (London), 2020-10, Vol.586 (7831), p.749-756

2020

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GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach

Bioinformatics, 2015-08, Vol.31 (16), p.2601-2606

2015

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Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

Nature medicine, 2021-11, Vol.27 (11), p.1876-1884

2021

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Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections

American journal of human genetics, 2016-09, Vol.99 (3), p.762-769

2016

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Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts

Nature genetics, 2020-06, Vol.52 (6), p.634-639

2020

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Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program

Nature genetics, 2018-11, Vol.50 (11), p.1514-1523

2018

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Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents

PloS one, 2021-02, Vol.16 (2), p.e0246447-e0246447

2021

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Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study)

PLoS medicine, 2020-12, Vol.17 (12), p.e1003452

2020

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Identification of cell type specific ACE2 modifiers by CRISPR screening

PLoS pathogens, 2022-03, Vol.18 (3), p.e1010377

2022

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Genome-scale CRISPR screening for modifiers of cellular LDL uptake

PLoS genetics, 2021-01, Vol.17 (1), p.e1009285-e1009285

2021

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A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study

European heart journal, 2022-05, Vol.43 (18), p.1702-1711

2022

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METAL: fast and efficient meta-analysis of genomewide association scans

Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

Unravelling the genetic architecture of human complex traits through whole genome sequencing

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

LocusZoom: regional visualization of genome-wide association scan results

Exploring and visualizing large-scale genetic associations by using PheWeb

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Genotype imputation

Causal relationships between NAFLD, T2D and obesity have implications for disease subphenotyping

Electronic health records: the next wave of complex disease genetics

The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities

Exome sequencing and characterization of 49,960 individuals in the UK Biobank

GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach

Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections

Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts

Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program

Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents

Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study)

Identification of cell type specific ACE2 modifiers by CRISPR screening

Genome-scale CRISPR screening for modifiers of cellular LDL uptake

A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study

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