Chapter 11: Genome-Wide Association Studies

Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

(2010) Marylyn D. Ritchie et al.   AMERICAN JOURNAL OF HUMAN GENETICS

PERMORY: an LD-exploiting permutation test algorithm for powerful genome-wide association testing

(2010) R. Pahl et al.   BIOINFORMATICS

Identification of Genomic Predictors of Atrioventricular Conduction

(2010) Joshua C. Denny et al.   CIRCULATION

Genes associated with multiple sclerosis: 15 and counting

(2010) Mario Habek et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease

(2010) Iftikhar J Kullo et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Integrating common and rare genetic variation in diverse human populations

(2010)   NATURE

Biological, clinical and population relevance of 95 loci for blood lipids

(2010) Tanya M. Teslovich et al.   NATURE

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

Evaluation of the Age-Related Eye Disease Study Clinical Lens Grading SystemAREDS Report No. 31

(2010) Emily Y. Chew et al.   OPHTHALMOLOGY

Biobanking and pharmacogenomics

(2010) Catherine A McCarty et al.   PHARMACOGENOMICS

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

(2009) Brian L. Browning et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genotype Imputation

(2009) Yun Li et al.   Annual Review of Genomics and Human Genetics

INTERSNP: genome-wide interaction analysis guided by a priori information

(2009) C. Herold et al.   BIOINFORMATICS

Meta-analysis in genome-wide association studies

(2009) Eleftheria Zeggini et al.   PHARMACOGENOMICS

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

(2009) L. A. Hindorff et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose

(2008) G. M. Cooper et al.   BLOOD

PRESTO: Rapid calculation of order statistic distributions and multiple-testing adjusted P-values via permutation for one and two-stage genetic association studies

(2008) Brian L Browning   BMC BIOINFORMATICS

Evaluation of coverage variation of SNP chips for genome-wide association studies

(2008) Mingyao Li et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Estimation of significance thresholds for genomewide association scans

(2008) Frank Dudbridge et al.   GENETIC EPIDEMIOLOGY

Commentary: Heterogeneity in meta-analysis should be expected and appropriately quantified

(2008) J. P T Higgins   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Common variants in the GDF5-UQCC region are associated with variation in human height

(2008) Serena Sanna et al.   NATURE GENETICS

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

(2008) Cristen J Willer et al.   NATURE GENETICS

Practical Issues in Imputation-Based Association Mapping

(2008) Yongtao Guan et al.   PLoS Genetics

Controlling false discoveries in genetic studies

(2007) Edwin J.C.G. van den Oord   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS