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Nature Communications|December 10, 2015
Long-term neural and physiological phenotyping of a single humanRussell A Poldrack, Timothy O Laumann, Oluwasanmi Koyejo, et al.
Lipids in Health and Disease|September 22, 2021
APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groupsShiwali Goyal, Yosuke Tanigawa, Weihua Zhang, et al.
Proceedings. IEEE International Symposium on Biomedical Imaging|September 18, 2025
COMBINING META- AND MEGA- ANALYTIC APPROACHES FOR MULTI-SITE DIFFUSION IMAGING BASED GENETIC STUDIES: FROM THE ENIGMA-DTI WORKING GROUPNeda Jahanshad, Peter Kochunov, Thomas E Nichols, et al.
American Journal of Human Genetics|October 1, 2019
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine ProgramChloé Sarnowski, Aaron Leong, Laura M Raffield, et al.
Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participantsLincoln Mp Shade, Mohsen Sharifitabar, Alexa Beiser, et al.
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2025
Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleedingRachel K Friedman, Adam S Heath, Jennifer E Huffman, et al.
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