Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

The Precision Medicine Initiative’s All of Us Research Program: an agenda for research on its ethical, legal, and social issues

(2016) Pamela L. Sankar et al.   GENETICS IN MEDICINE

The genetic architecture of type 2 diabetes

(2016) Christian Fuchsberger et al.   NATURE

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

(2015) J. E. Huffman et al.   BLOOD

WGSA: an annotation pipeline for human genome sequencing studies

(2015) Xiaoming Liu et al.   JOURNAL OF MEDICAL GENETICS

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

(2014) Jeffrey G Reid et al.   BMC BIOINFORMATICS

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

Whole-genome sequence–based analysis of high-density lipoprotein cholesterol

(2013) Alanna C Morrison et al.   NATURE GENETICS

An integrated encyclopedia of DNA elements in the human genome

(2012)   NATURE

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

(2011) Michael C. Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

(2009) Bruce M. Psaty et al.   Circulation-Cardiovascular Genetics