Disease-Concordant Twins Empower Genetic Association Studies

Twin methodology in epigenetic studies

(2015) Q. Tan et al.   JOURNAL OF EXPERIMENTAL BIOLOGY

Genetic linkage analysis in the age of whole-genome sequencing

(2015) Jurg Ott et al.   NATURE REVIEWS GENETICS

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

(2015) Raffaele Ferrari et al.   NEUROBIOLOGY OF AGING

Rare-Variant Association Analysis: Study Designs and Statistical Tests

(2014) Seunggeung Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Technology: The $1,000 genome

(2014) Erika Check Hayden   NATURE

An atlas of genetic influences on human blood metabolites

(2014) So-Youn Shin et al.   NATURE GENETICS

Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease

(2013) Martin Dichgans et al.   STROKE

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

(2012) J. A. Tennessen et al.   SCIENCE

An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

(2012) M. R. Nelson et al.   SCIENCE

Power assessment for genetic association study of human longevity using offspring of long-lived subjects

(2010) Qihua Tan et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

Replication in Genome-Wide Association Studies

(2010) Peter Kraft et al.   STATISTICAL SCIENCE

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip

(2009) Chris C. A. Spencer et al.   PLoS Genetics

Power for Genetic Association Study of Human Longevity Using the Case-Control Design

(2008) Q. Tan et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

Personal genomes: The case of the missing heritability

(2008) Brendan Maher   NATURE