Joshua C. Denny, M.D., M.S.
Affiliations: | Biomedical Informatics | Vanderbilt University School of Medicine, Nashville, TN, United States |
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"Joshua Denny"Cross-listing: Biomedical Informatics
Parents
Sign in to add mentorRandolph A. Miller | grad student | Vanderbilt Medical School (Biomedical Informatics) | |
Dan Roden | grad student | Vanderbilt (Cell Biology Tree) |
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Publications
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Schlueter DJ, Sulieman L, Mo H, et al. (2023) Systematic replication of smoking disease associations using survey responses and EHR data in the All of Us Research Program. Journal of the American Medical Informatics Association : Jamia |
Deflaux N, Selvaraj MS, Condon HR, et al. (2023) Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis. Nature Communications. 14: 5419 |
Schuler BA, Bastarache L, Wang J, et al. (2023) Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection. Plos One. 18: e0286469 |
Cassini T, Bastarache L, Zeng C, et al. (2023) A Test of Automated Use of Electronic Health Records to Aid in Diagnosis of Genetic Disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100966 |
Bastarache L, Delozier S, Pandit A, et al. (2023) The phenotype-genotype reference map: Improving biobank data science through replication. American Journal of Human Genetics |
Mayo KR, Basford MA, Carroll RJ, et al. (2023) The Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research. Annual Review of Biomedical Data Science. 6: 443-464 |
Allaire P, He J, Mayer J, et al. (2023) Genetic and clinical determinants of telomere length. Hgg Advances. 4: 100201 |
Joo YY, Pacheco JA, Thompson WK, et al. (2023) Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Plos One. 18: e0283553 |
Suzuki K, Hatzikotoulas K, Southam L, et al. (2023) Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Medrxiv : the Preprint Server For Health Sciences |
Schulkey CE, Litwin TR, Ellsworth G, et al. (2023) Design and Implementation of the All of Us Research Program COVID-19 Participant Experience (COPE) Survey. American Journal of Epidemiology |