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Molecular Genetics & Genomic Medicine|September 22, 2016
Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African AmericansRoxana Daneshjou, Larisa H Cavallari, Peter E Weeke, et al.American Journal of Human Genetics|April 2, 2021
Opportunities and challenges for the computational interpretation of rare variation in clinically important genesGregory McInnes, Andrew G Sharo, Megan L Koleske, et al.Annals of Internal Medicine|November 23, 2006
Pharmacogenomics: challenges and opportunitiesDan M Roden, Russ B Altman, Neal L Benowitz, et al.Genome Biology|October 18, 2008
Text mining for biology--the way forward: opinions from leading scientistsRuss B Altman, Casey M Bergman, Judith Blake, et al.BMC Genomics|July 4, 2013
Pathway analysis of genome-wide data improves warfarin dose predictionRoxana Daneshjou, Nicholas P Tatonetti, Konrad J Karczewski, et al.RNA (New York, N.Y.)|February 18, 2006
The RNA Ontology Consortium: an open invitation to the RNA communityNeocles B Leontis, Russ B Altman, Helen M Berman, et al.Plos Genetics|October 9, 2015
Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence DataFrederick E Dewey, Megan E Grove, James R Priest, et al.Nature Medicine|April 19, 2016
Human induced pluripotent stem cell-derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicityPaul W Burridge, Yong Fuga Li, Elena Matsa, et al.Bioinformatics (Oxford, England)|June 20, 2019
PatientExploreR: an extensible application for dynamic visualization of patient clinical history from electronic health records in the OMOP common data modelBenjamin S Glicksberg, Boris Oskotsky, Phyllis M Thangaraj, et al.Science Translational Medicine|April 22, 2016
A research roadmap for next-generation sequencing informaticsRuss B Altman, Snehit Prabhu, Arend Sidow, et al.Pageof 32