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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2019
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panelTheodore Chiang, Xiuping Liu, Tsung-Jung Wu, et al.Diabetes|October 9, 2008
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetesStruan F A Grant, Hui-Qi Qu, Jonathan P Bradfield, et al.The Journal of Clinical Endocrinology and Metabolism|January 10, 2020
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association StudiesYoonjung Yoonie Joo, Ky'Era Actkins, Jennifer A Pacheco, et al.American Journal of Human Genetics|April 30, 2024
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE NetworkAnna C F Lewis, Rex L Chisholm, John J Connolly, et al.Scientific Reports|May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiologyJonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.American Journal of Respiratory and Critical Care Medicine|September 23, 2020
Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African AmericansHongsheng Gui, Albert M Levin, Donglei Hu, et al.Diabetes|January 17, 2008
A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association studyHakon Hakonarson, Hui-Qi Qu, Jonathan P Bradfield, et al.American Journal of Human Genetics|April 30, 2026
Navigating data sharing in researchAnna C F Lewis, Ellen W Clayton, Hana Bangash, et al.American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.Pageof 91