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Unified representation of genetic variants

Bioinformatics, 2015-07, Vol.31 (13), p.2202-2204

2015

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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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Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Nature genetics, 2012-08, Vol.44 (8), p.955-959

2012

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minimac2: faster genotype imputation

Bioinformatics (Oxford, England), 2015-03, Vol.31 (5), p.782-784

2015

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An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

Genome research, 2015-06, Vol.25 (6), p.918

2015

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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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Genotype Imputation from Large Reference Panels

Annual review of genomics and human genetics, 2018-08, Vol.19 (1), p.73-96

2018

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Age-Related Macular Degeneration: Genetics and Biology Coming Together

Annual review of genomics and human genetics, 2014-01, Vol.15 (1), p.151-171

2014

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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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Family-Based Association Tests for Genomewide Association Scans

American journal of human genetics, 2007-11, Vol.81 (5), p.913-926

2007

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Low-coverage sequencing: implications for design of complex trait association studies

Genome research, 2011-06, Vol.21 (6), p.940

2011

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Improved Ancestry Estimation for both Genotyping and Sequencing Data using Projection Procrustes Analysis and Genotype Imputation

American journal of human genetics, 2015-06, Vol.96 (6), p.926-937

2015

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Nature reviews. Genetics, 2008-05, Vol.9 (5), p.356-369

2008

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Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data

American journal of human genetics, 2012-11, Vol.91 (5), p.839-848

2012

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Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Nature genetics, 2018-05, Vol.50 (5), p.737-745

2018

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Next-generation genotype imputation service and methods

Nature genetics, 2016-10, Vol.48 (10), p.1284-1287

2016

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Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study

PLoS genetics, 2009-01, Vol.5 (1), p.e1000338-e1000338

2009

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Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative

American journal of human genetics, 2018-06, Vol.102 (6), p.1048-1061

2018

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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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Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry

Nature neuroscience, 2018-01, Vol.21 (1), p.16

2018

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Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration

Nature genetics, 2019-04, Vol.51 (4), p.606-610

2019

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Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

Nature genetics, 2015-11, Vol.47 (11), p.1272-1281

2015

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RAREMETAL: fast and powerful meta-analysis for rare variants

Bioinformatics (Oxford, England), 2014-10, Vol.30 (19), p.2828-2829

2014

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Unified representation of genetic variants

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

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

minimac2: faster genotype imputation

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

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

Genotype Imputation from Large Reference Panels

Age-Related Macular Degeneration: Genetics and Biology Coming Together

LocusZoom: regional visualization of genome-wide association scan results

Family-Based Association Tests for Genomewide Association Scans

Low-coverage sequencing: implications for design of complex trait association studies

Improved Ancestry Estimation for both Genotyping and Sequencing Data using Projection Procrustes Analysis and Genotype Imputation

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Next-generation genotype imputation service and methods

Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study

Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative

Exploring and visualizing large-scale genetic associations by using PheWeb

Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

RAREMETAL: fast and powerful meta-analysis for rare variants

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