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Alzheimer Disease and Associated Disorders|October 23, 2025
Evaluation of Polygenic Risk Scores for a Possible Genetic Basis of the Inverse Association Between Cancer and Cognitive DeclineRebecca E Graff, Dorothy M Chen, Kaitlin N Swinnerton, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|January 29, 2017
Familial Risk and Heritability of Colorectal Cancer in the Nordic Twin Study of CancerRebecca E Graff, Sören Möller, Michael N Passarelli, et al.
Nature Communications|April 26, 2016
Identifying genetically driven clinical phenotypes using linear mixed modelsJonathan D Mosley, John S Witte, Emma K Larkin, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
The full spectrum of OCT1 (SLC22A1) mutations bridges transporter biophysics to drug pharmacogenomicsSook Wah Yee, Christian Macdonald, Darko Mitrovic, et al.
American Journal of Medical Genetics. Part A|April 22, 2022
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention StudySara R Rashkin, Mario Cleves, Gary M Shaw, et al.
Pediatrics|July 31, 2013
A genome-wide association study (GWAS) for bronchopulmonary dysplasiaHui Wang, Krystal R St Julien, David K Stevenson, et al.
HGG Advances|February 6, 2025
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Journal of Clinical Medicine|July 29, 2023
Catheter-Based Techniques for Addressing Atrioventricular Valve Regurgitation in Adult Congenital Heart Disease Patients: A Descriptive CohortAbdelhak El Bouziani, Lars S Witte, Berto J Bouma, et al.
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