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Unified representation of genetic variants

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

2015

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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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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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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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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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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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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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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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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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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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Ancestry estimation and control of population stratification for sequence-based association studies

Nature genetics, 2014-04, Vol.46 (4), p.409-415

2014

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variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (41), p.16227-16232

2007

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Meta-analysis of gene-level tests for rare variant association

Nature genetics, 2014-02, Vol.46 (2), p.200-204

2014

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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (5), p.1620-1625

2008

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A likelihood-based framework for variant calling and de novo mutation detection in families

PLoS genetics, 2012-10, Vol.8 (10), p.e1002944-e1002944

2012

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Pervasive sharing of genetic effects in autoimmune disease

PLoS genetics, 2011-08, Vol.7 (8), p.e1002254-e1002254

2011

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Unified representation of genetic variants

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

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

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

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

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

Complex genetic signatures in immune cells underlie autoimmunity and inform therapy

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

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

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

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

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

Ancestry estimation and control of population stratification for sequence-based association studies

variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration

Meta-analysis of gene-level tests for rare variant association

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

A likelihood-based framework for variant calling and de novo mutation detection in families

Pervasive sharing of genetic effects in autoimmune disease

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