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Human Genomics|April 5, 2025
Experiences of participants with undiagnosed diseases and hereditary cancers during the initial phase of the Hong Kong genome project: a mixed-methods studyAnnie Tw Chu, Samuel Yc Sze, Desiree Ms Tse, et al.Human Genomics|April 25, 2025
Pharmacogenomic insights into atorvastatin and rosuvastatin adverse effects: a prospective observational study in the UAE's multiethnic populationMais N Alqasrawi, Zeina N Al-Mahayri, Areej S AlBawa'neh, et al.Human Genomics|April 26, 2025
Expression of concern for global biomedical research by the human genome organization (HUGO)Ada Hamosh, Fabiana Arzuaga, Karen B Avraham, et al.Human Genomics|April 1, 2025
A comparison of the expression patterns and diagnostic capability of the ncRNAs NEAT1 and miR-34a in non-obstructive azoospermia and severe oligospermiaAya Salman, Abdullah F Radwan, Olfat G Shaker, et al.Human Genomics|June 18, 2025
Outcomes of genetic testing for Usher syndrome in a diverse population cohort from South FloridaZachary J Cromar, Ryan Chen, Tamara Juvier Riesgo, et al.Human Genomics|May 20, 2025
Genetic counseling in the Middle East: provider perspectives of patient attitudes and cultural challengesShruti Shenbagam, Alan Taylor, Ruchi Jain, et al.Human Genomics|June 11, 2025
Improved breast cancer risk prediction using chromosomal-scale length variationYasaman Fatapour, James P BrodyHuman Genomics|May 9, 2025
Genetic variants of m1A modification genes and the risk of neuroblastoma: novel insights from a Chinese case-control studyJiaming Chang, Lei Lin, Wenli Zhang, et al.Human Genomics|May 12, 2025
Bioinformatics analysis of circular RNAs associated with atrial fibrillation and their evaluation as predictive biomarkersManman Wang, Yuanyuan Chen, Weiwei Yang, et al.Human Genomics|January 31, 2026
Elucidating the genetic landscape of inherited retinal disorders in IndiaGrace Priyaranjini Mathias, Kadarkarai Raj Rajendran, Ruchita Selot, et al.Pageof 112