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Blood Cancer Discovery|May 22, 2025
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangementsGabriele Varano, Silvia Lonardi, Paola Sindaco, et al.
Journal of Translational Medicine|June 23, 2023
Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)Filippo Pinto E Vairo, Jennifer L Kemppainen, Carolyn R Rohrer Vitek, et al.
Nature Human Behaviour|April 23, 2021
The general fault in our fault linesKai Ruggeri, Bojana Većkalov, Lana Bojanić, et al.
Nature|February 23, 2002
The genome sequence of Schizosaccharomyces pombeV Wood, R Gwilliam, M-A Rajandream, et al.
Nature Human Behaviour|July 11, 2022
The globalizability of temporal discountingKai Ruggeri, Amma Panin, Milica Vdovic, et al.
American Journal of Human Genetics|December 18, 2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer SubtypesNasim Mavaddat, Kyriaki Michailidou, Joe Dennis, et al.
BMC Biology|February 6, 2025
Same data, different analysts: variation in effect sizes due to analytical decisions in ecology and evolutionary biologyElliot Gould, Hannah S Fraser, Timothy H Parker, et al.
Nature Genetics|January 9, 2020
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genesLaura Fachal, Hugues Aschard, Jonathan Beesley, et al.
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