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Nature Genetics|March 26, 2013
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexityAustin M Dulak, Petar Stojanov, Shouyong Peng, et al.Circulation. Genomic and Precision Medicine|March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine ProgramAmanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.Science (New York, N.Y.)|July 30, 2011
The mutational landscape of head and neck squamous cell carcinomaNicolas Stransky, Ann Marie Egloff, Aaron D Tward, et al.Circulation. Cardiovascular Genetics|April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of conceptKiran Musunuru, Guillaume Lettre, Taylor Young, et al.Human Genetics|March 20, 2014
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African AmericansJaclyn Ellis, Ethan M Lange, Jin Li, et al.Cell|July 24, 2012
A landscape of driver mutations in melanomaEran Hodis, Ian R Watson, Gregory V Kryukov, et al.American Journal of Respiratory and Critical Care Medicine|June 27, 2024
Dysanapsis Genetic Risk Predicts Lung Function Across the LifespanCatherine L Debban, Amirthagowri Ambalavanan, Auyon Ghosh, et al.Nature Genetics|November 6, 2007
Two independent alleles at 6q23 associated with risk of rheumatoid arthritisRobert M Plenge, Chris Cotsapas, Leela Davies, et al.Nature|February 11, 2011
The genomic complexity of primary human prostate cancerMichael F Berger, Michael S Lawrence, Francesca Demichelis, et al.Molecular Psychiatry|March 5, 2008
Whole-genome association study of bipolar disorderP Sklar, J W Smoller, J Fan, et al.Pageof 28