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Medrxiv : the Preprint Server for Health Sciences|June 29, 2026
Elective genomic sequencing for adults in research, clinical and commercial contextsMichael D Linderman, Sophia M Adelson, Tala M Berro, et al.JAMA Oncology|October 30, 2020
Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer SyndromeN Jewel Samadder, Douglas Riegert-Johnson, Lisa Boardman, 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.Nature|July 19, 2023
Organization of the human intestine at single-cell resolutionJohn W Hickey, Winston R Becker, Stephanie A Nevins, et al.Nature Cancer|October 31, 2024
Multiomic analysis of familial adenomatous polyposis reveals molecular pathways associated with early tumorigenesisEdward D Esplin, Casey Hanson, Si Wu, et al.Circulation. Genomic and Precision Medicine|January 22, 2021
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial HypercholesterolemiaGemme Campbell-Salome, Laney K Jones, Max F Masnick, et al.Cell|April 18, 2020
The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell ResolutionOrit Rozenblatt-Rosen, Aviv Regev, Philipp Oberdoerffer, et al.Nature|November 25, 2025
Polyclonal origins of human premalignant colorectal lesionsDebra Van Egeren, Ryan O Schenck, Aziz Khan, et al.Biorxiv : the Preprint Server for Biology|November 26, 2025
Polyclonal origins of human premalignant colorectal lesionsDebra Van Egeren, Ryan O Schenck, Aziz Khan, et al.American Journal of Human Genetics|March 24, 2026
The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessmentsNita Limdi, T Mark Beasley, Josh Cortopassi, et al.Pageof 10