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Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Genetic association studies using disease liabilities from deep neural networksLu Yang, Marie C Sadler, Russ B AltmanAmerican Journal of Human Genetics|February 22, 2025
Genetic association studies using disease liabilities from deep neural networksLu Yang, Marie C Sadler, Russ B AltmanCambridge Prisms. Precision Medicine|August 10, 2023
Promises and challenges in pharmacoepigeneticsDelaney A Smith, Marie C Sadler, Russ B AltmanPacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 13, 2024
Identifying DNA methylation sites affecting drug response using electronic health record-derived GWAS summary statisticsDelaney A Smith, Stephanie A Arteaga, Marie C Sadler, et al.Journal of the American Medical Informatics Association : JAMIA|December 5, 2022
POPDx: an automated framework for patient phenotyping across 392 246 individuals in the UK Biobank studyLu Yang, Sheng Wang, Russ B AltmanMedrxiv : the Preprint Server for Health Sciences|April 18, 2024
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medicationsMarie C Sadler, Alexander Apostolov, Caterina Cevallos, et al.Nature Communications|March 26, 2025
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medicationsMarie C Sadler, Alexander Apostolov, Caterina Cevallos, et al.Clinical Pharmacology and Therapeutics|November 15, 2017
Challenges for Training Translational Researchers in the Era of Ubiquitous DataRuss B AltmanCurrent Opinion in Drug Discovery & Development|July 2, 2003
Genetic sequence data for pharmacogenomicsRuss B AltmanPageof 373