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Nature Genetics|November 8, 2016
Prospective functional classification of all possible missense variants in PPARGAmit R Majithia, Ben Tsuda, Maura Agostini, et al.Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.Heart Rhythm|June 12, 2012
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization patternMoritz F Sinner, Kimmo Porthan, Peter A Noseworthy, et al.American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.Nature Cardiovascular Research|May 31, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcificationPaul S de Vries, Matthew P Conomos, Kuldeep Singh, et al.Science (New York, N.Y.)|July 16, 2026
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.Nature Genetics|April 5, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementiasCéline Bellenguez, Fahri Küçükali, Iris E Jansen, et al.American Journal of Human Genetics|August 5, 2022
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsShweta Ramdas, Jonathan Judd, Sarah E Graham, et al.Pageof 2