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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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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.918-925

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

Genome research, 2011-06, Vol.21 (6), p.940-951

2011

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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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Complex genetic signatures in immune cells underlie autoimmunity and inform therapy

Nature genetics, 2020-10, Vol.52 (10), p.1036-1045

2020

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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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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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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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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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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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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 of delay discounting in 23,217 adult research participants of European ancestry

Nature neuroscience, 2018-01, Vol.21 (1), p.16-18

2018

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A comparison of approaches to account for uncertainty in analysis of imputed genotypes

Genetic epidemiology, 2011-02, Vol.35 (2), p.102-110

2011

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A genome-wide association study of global gene expression

Nature genetics, 2007-10, Vol.39 (10), p.1202-1207

2007

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Merlin-rapid analysis of dense genetic maps using sparse gene flow trees

Nature genetics, 2002-01, Vol.30 (1), p.97-101

2002

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Genetic Testing in Persons with Age-Related Macular Degeneration and the Use of the AREDS Supplements: To Test or Not to Test?

Ophthalmology (Rochester, Minn.), 2015-01, Vol.122 (1), p.212-215

2015

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Ancestry-agnostic estimation of DNA sample contamination from sequence reads

Genome research, 2020-02, Vol.30 (2), p.185-194

2020

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Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

Nature, 2007-07, Vol.448 (7152), p.470-473

2007

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Genome-wide association analysis identifies three psoriasis susceptibility loci

Nature genetics, 2010-11, Vol.42 (11), p.1000-1004

2010

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

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

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

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

Complex genetic signatures in immune cells underlie autoimmunity and inform therapy

Next-generation genotype imputation service and methods

Exploring and visualizing large-scale genetic associations by using PheWeb

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

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

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

Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways

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

A comparison of approaches to account for uncertainty in analysis of imputed genotypes

A genome-wide association study of global gene expression

Merlin-rapid analysis of dense genetic maps using sparse gene flow trees

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Genetic Testing in Persons with Age-Related Macular Degeneration and the Use of the AREDS Supplements: To Test or Not to Test?

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

Genome-wide association analysis identifies three psoriasis susceptibility loci

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