Showing results (11-20 of 33) with videos related to
Sort By:
Pageof 4
Database : the Journal of Biological Databases and Curation|September 25, 2025
Biomedical literature-based clinical phenotype definition discovery using large language modelsSamar Binkheder, Xiaofu Liu, Michael Wu, et al.The American Journal of Cardiology|June 1, 2016
Effect of Left Ventricular Systolic Dysfunction on Response to WarfarinSameer Ather, Aditi Shendre, T Mark Beasley, et al.IEEE/ACM Transactions on Computational Biology and Bioinformatics|August 24, 2019
Improved Adverse Drug Event Prediction Through Information Component Guided Pharmacological Network Model (IC-PNM)Xiangmin Ji, Lei Wang, Liyan Hua, et al.Oncotarget|February 10, 2018
A plasma telomeric cell-free DNA level in unaffected women with BRCA1 or/and BRCA2 mutations: a pilot studyShatovisha Dey, Natascia Marino, Kanokwan Bishop, et al.Plos One|October 27, 2010
Interleukin-10 (IL-10) pathway: genetic variants and outcomes of HIV-1 infection in African American adolescentsSadeep Shrestha, Howard W Wiener, Brahim Aissani, et al.Pragmatic and Observational Research|December 25, 2024
Detection of Patient-Level Immunotherapy-Related Adverse Events (irAEs) from Clinical Narratives of Electronic Health Records: A High-Sensitivity Artificial Intelligence ModelMd Muntasir Zitu, Margaret E Gatti-Mays, Kai C Johnson, et al.Pharmacotherapy|October 1, 2025
Identifying Pediatric Drug Safety Knowledge Gaps: An Integrated Approach Leveraging Real-World Data, a Biomedical Knowledge Base, and Postmarketing Surveillance DataSaurabh Rahurkar, Jiayi Ouyang, Pallavi Jonnalagadda, et al.Pharmacotherapy|February 16, 2016
Race-Specific Influence of CYP4F2 on Dose and Risk of Hemorrhage Among Warfarin UsersAditi Shendre, Todd M Brown, Nianjun Liu, et al.Pharmacogenetics and Genomics|June 20, 2013
FcγR gene copy number in Kawasaki disease and intravenous immunoglobulin treatment responseRobert Makowsky, Howard W Wiener, Travis S Ptacek, et al.Journal of Human Genetics|December 16, 2014
Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individualsDegui Zhi, Aditi Shendre, Rebecca Scherzer, et al.Pageof 4