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NPJ Digital Medicine|July 16, 2019
Finding missed cases of familial hypercholesterolemia in health systems using machine learningJuan M Banda, Ashish Sarraju, Fahim Abbasi, et al.
Nature Genetics|May 31, 2022
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic diseaseCatherine Tcheandjieu, Ke Xiao, Helio Tejeda, et al.
Journal of Lipid Research|November 24, 2007
Effects of the cholesteryl ester transfer protein inhibitor torcetrapib on VLDL apolipoprotein E metabolismJohn S Millar, Margaret E Brousseau, Margaret R Diffenderfer, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|January 10, 2022
Early prediction of decompensation (EPOD) score: Non-invasive determination of cirrhosis decompensation riskAnnika R P Schneider, Carolin V Schneider, Kai Markus Schneider, et al.
European Journal of Medical Genetics|November 15, 2025
An electronic review of clinical outcomes after return of actionable genetic research results from a health system research biobankGiorgio Cocchella, Lillian Phung, Elisabeth Wood, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 10, 2021
Heritability of quantitative autism spectrum traits in adults: A family-based studySara C Taylor, Samantha Steeman, Brielle N Gehringer, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2017
A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and PancreatitisMasako Ueda, Richard L Dunbar, Anna Wolska, et al.
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