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Genomewide Association Studies — Illuminating Biologic Pathways

The New England journal of medicine, 2009-04, Vol.360 (17), p.1699-1701

Hirschhorn, Joel N

2009

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Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations

Nature communications, 2020-03, Vol.11 (1), p.1467-1467, Article 1467

2020

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SNPsnap: a Web-based tool for identification and annotation of matched SNPs

Bioinformatics, 2015-02, Vol.31 (3), p.418-420

2015

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Genome-wide association studies for common diseases and complex traits

Nature reviews. Genetics, 2005-02, Vol.6 (2), p.95-108

2005

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Biological interpretation of genome-wide association studies using predicted gene functions

Nature communications, 2015-01, Vol.6 (1), p.5890-5890, Article 5890

2015

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Genetic Evaluation of Short Stature

The journal of clinical endocrinology and metabolism, 2014-09, Vol.99 (9), p.3080-3092

2014

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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

Nature genetics, 2012-04, Vol.44 (4), p.369-375

2012

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Post-translational control of beige fat biogenesis by PRDM16 stabilization

Nature (London), 2022-09, Vol.609 (7925), p.151-158

2022

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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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Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders

American journal of human genetics, 2016-09, Vol.99 (3), p.527-539

2016

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Interrogation of human hematopoiesis at single-cell and single-variant resolution

Nature genetics, 2019-04, Vol.51 (4), p.683-693

2019

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Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases

Nature genetics, 2023-08, Vol.55 (8), p.1267-1276

2023

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The history of African gene flow into Southern Europeans, Levantines, and Jews

PLoS genetics, 2011-04, Vol.7 (4), p.e1001373-e1001373

2011

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Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels

Nature genetics, 2016-04, Vol.48 (4), p.359-366

2016

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Short Stature, Accelerated Bone Maturation, and Early Growth Cessation Due to Heterozygous Aggrecan Mutations

The journal of clinical endocrinology and metabolism, 2014-08, Vol.99 (8), p.E1510-E1518

2014

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Improved ancestry inference using weights from external reference panels

Bioinformatics, 2013-06, Vol.29 (11), p.1399-1406

2013

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SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant

American journal of human genetics, 2013-11, Vol.93 (5), p.798-811

2013

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Nature genetics, 2003-02, Vol.33 (2), p.177-182

2003

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Genetic model testing and statistical power in population-based association studies of quantitative traits

Genetic epidemiology, 2007-05, Vol.31 (4), p.358-362

2007

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Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Cell stem cell, 2016-01, Vol.18 (1), p.73-78

2016

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Genetic association studies of complex traits: design and analysis issues

Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis, 2005-06, Vol.573 (1), p.54-69

2005

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DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

Proceedings of the National Academy of Sciences - PNAS, 2008-08, Vol.105 (33), p.11869-11874

2008

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Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies

Nature genetics, 2010-07, Vol.42 (7), p.626-630

2010

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A positively selected FBN1 missense variant reduces height in Peruvian individuals

Nature (London), 2020-06, Vol.582 (7811), p.234-239

2020

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Genome-wide analysis of body proportion classifies height-associated variants by mechanism of action and implicates genes important for skeletal development

American journal of human genetics, 2015-05, Vol.96 (5), p.695-708

2015

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Genomewide Association Studies — Illuminating Biologic Pathways

Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations

SNPsnap: a Web-based tool for identification and annotation of matched SNPs

Genome-wide association studies for common diseases and complex traits

Biological interpretation of genome-wide association studies using predicted gene functions

Genetic Evaluation of Short Stature

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

Post-translational control of beige fat biogenesis by PRDM16 stabilization

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

Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders

Interrogation of human hematopoiesis at single-cell and single-variant resolution

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases

The history of African gene flow into Southern Europeans, Levantines, and Jews

Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels

Short Stature, Accelerated Bone Maturation, and Early Growth Cessation Due to Heterozygous Aggrecan Mutations

Improved ancestry inference using weights from external reference panels

SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Genetic model testing and statistical power in population-based association studies of quantitative traits

Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Genetic association studies of complex traits: design and analysis issues

DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies

A positively selected FBN1 missense variant reduces height in Peruvian individuals

Genome-wide analysis of body proportion classifies height-associated variants by mechanism of action and implicates genes important for skeletal development

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