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Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

American journal of human genetics, 2011-07, Vol.89 (1), p.82-93

2011

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Non―invasive prenatal measurement of the fetal genome

Nature (London), 2012-07, Vol.487 (7407), p.320-324

2012

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Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: U.S. Preventive Services Task Force Recommendation Statement

Annals of internal medicine, 2014-02, Vol.160 (4), p.271

Moyer, Virginia A.

2014

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GCTA: A Tool for Genome-wide Complex Trait Analysis

American journal of human genetics, 2011-01, Vol.88 (1), p.76-82

2011

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Five Years of GWAS Discovery

American journal of human genetics, 2012-01, Vol.90 (1), p.7-24

2012

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Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer

Journal of clinical oncology, 2014-03, Vol.32 (7), p.618-626

2014

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PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

American journal of human genetics, 2007-09, Vol.81 (3), p.559-575

2007

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Abundant Pleiotropy in Human Complex Diseases and Traits

American journal of human genetics, 2011-11, Vol.89 (5), p.607-618

2011

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Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

American journal of human genetics, 2010-06, Vol.86 (6), p.832-838

2010

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Estimating Missing Heritability for Disease from Genome-wide Association Studies

American journal of human genetics, 2011-03, Vol.88 (3), p.294-305

2011

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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

Journal of medical genetics, 2011-12, Vol.48 (12), p.856-859

2011

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Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: A Systematic Review to Update the U.S. Preventive Services Task Force Recommendation

Annals of internal medicine, 2014-02, Vol.160 (4), p.255

2014

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DECIPHER : Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

American journal of human genetics, 2009-04, Vol.84 (4), p.524-533

2009

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Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

European heart journal, 2010-11, Vol.31 (22), p.2715-2726

2010

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Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering

American journal of human genetics, 2007-11, Vol.81 (5), p.1084-1097

2007

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A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals

American journal of human genetics, 2009-02, Vol.84 (2), p.210-223

2009

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BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies

American journal of human genetics, 2010-09, Vol.87 (3), p.325-340

2010

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A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root

American journal of human genetics, 2012-04, Vol.90 (4), p.675-684

2012

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Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis

American journal of human genetics, 2011-09, Vol.89 (3), p.432-437

2011

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A Versatile Gene-Based Test for Genome-wide Association Studies

American journal of human genetics, 2010-07, Vol.87 (1), p.139-145

2010

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Denisova Admixture and the First Modern Human Dispersals into Southeast Asia and Oceania

American journal of human genetics, 2011-10, Vol.89 (4), p.516-528

2011

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Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

American journal of human genetics, 2012-01, Vol.90 (1), p.119-124

2012

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Walking the Interactome for Prioritization of Candidate Disease Genes

American journal of human genetics, 2008-04, Vol.82 (4), p.949-958

2008

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Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.27-32

2012

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Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

Non―invasive prenatal measurement of the fetal genome

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: U.S. Preventive Services Task Force Recommendation Statement

GCTA: A Tool for Genome-wide Complex Trait Analysis

Five Years of GWAS Discovery

Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

Abundant Pleiotropy in Human Complex Diseases and Traits

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

Estimating Missing Heritability for Disease from Genome-wide Association Studies

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: A Systematic Review to Update the U.S. Preventive Services Task Force Recommendation

DECIPHER : Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering

A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals

BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies

A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root

Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis

A Versatile Gene-Based Test for Genome-wide Association Studies

Denisova Admixture and the First Modern Human Dispersals into Southeast Asia and Oceania

Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

Walking the Interactome for Prioritization of Candidate Disease Genes

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

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