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Nature Genetics|February 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.Cancer Research|July 2, 2026
A Clinically Integrated Pediatric Patient-Derived Xenograft Program Enables Evaluation of Cohort and Patient-Specific Biology and Therapeutic StrategiesFilemon S Dela Cruz, Daoqi You, Tamar Y Feinberg, et al.Clinical Journal of the American Society of Nephrology : CJASN|January 23, 2024
Histologic and Clinical Factors Associated with Kidney Outcomes in IgA Vasculitis NephritisSean J Barbour, Rosanna Coppo, Lee Er, et al.Nature Genetics|January 2, 2025
The impact of common and rare genetic variants on bradyarrhythmia developmentLu-Chen Weng, Joel T Rämö, Sean J Jurgens, et al.Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.Nature Communications|February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageLot Snijders Blok, Justine Rousseau, Joanna Twist, et al.Nature Communications|November 7, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageLot Snijders Blok, Justine Rousseau, Joanna Twist, et al.Nature Communications|May 4, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageLot Snijders Blok, Justine Rousseau, Joanna Twist, et al.Nature|February 7, 2020
Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.Nature Genetics|May 1, 2012
Meta-analysis identifies six new susceptibility loci for atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Christine M Albert, et al.Pageof 273