Peter S White

Use of an enterprise wiki as a research collaboration tool.

Bimal R Desai, Ryan T O'Hara, Peter S White, 2007, AMIA ... Annual Symposium proceedings. AMIA Symposium.

Structural variations in attention-deficit hyperactivity disorder

Hakon Hakonarson, Peter S White, H. Hakonarson, 2011, The Lancet.

Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data

Jeffrey Pennington, Mahdi Sarmady, Bo Zhang, 2018, Genetics in Medicine.

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

Yufeng Shen, Boris Yamrom, Jeremy Leipzig, 2014, Circulation research.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.

Xiaowu Gai, Joseph T. Glessner, Hakon Hakonarson, 2011, Congenital heart disease.

Genomic annotation of the meningioma tumor suppressor locus on chromosome 1p34

Peter S White, E. Sulman, P. White, 2004, Oncogene.

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Xiaowu Gai, Laura K Conlin, Livija Medne, 2009, Genome research.