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European Journal of Heart Failure|March 12, 2022
Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failureIain S Forrest, Ghislain Rocheleau, Shantanu Bafna, et al.
Genome Medicine|June 12, 2026
Genetically supported drug target prioritization for rare diseasesRobert Chen, Áine Duffy, Matthew Mort, et al.
Cell Reports Methods|December 10, 2024
Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human diseaseBen O Petrazzini, Daniel J Balick, Iain S Forrest, et al.
European Heart Journal. Digital Health|March 12, 2026
Three-year risk prediction of aortic stenosis using routine medical records: derivation and validation in 919 954 individuals from two cohortsBen O Petrazzini, Waqas A Malick, Stamatios Lerakis, et al.
Science Advances|September 12, 2020
Tissue-specific genetic features inform prediction of drug side effects in clinical trialsÁine Duffy, Marie Verbanck, Amanda Dobbyn, et al.
Communications Biology|August 20, 2022
A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK BiobankGhislain Rocheleau, Iain S Forrest, Áine Duffy, et al.
Journal of the American College of Cardiology|March 25, 2022
Coronary Risk Estimation Based on Clinical Data in Electronic Health RecordsBen O Petrazzini, Kumardeep Chaudhary, Carla Márquez-Luna, et al.
Cell Reports Methods|July 27, 2025
Genetic analyses of eight complex diseases using predicted continuous representations of diseaseRobert Chen, Ghislain Rocheleau, Ben Omega Petrazzini, et al.
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