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Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site StudyRune Boen, Kathleen P O'Hora, Hoki Fung, et al.
Nature Communications|March 15, 2023
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular diseaseWilliam J Young, Jeffrey Haessler, Jan-Walter Benjamins, et al.
Brain : a Journal of Neurology|November 15, 2025
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiencyKajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben, et al.
Cell|May 7, 2026
Multi-cohort proteogenomic analyses reveal genetic effects across the proteome and diseasomeMine Koprulu, Karl Smith-Byrne, Brian Richard Ferolito, et al.
Journal of the American College of Cardiology|June 22, 2019
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected IndividualsRaymond Noordam, William J Young, Reem Salman, et al.
Human Brain Mapping|February 22, 2021
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVsIda E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Physical Review Letters|May 2, 2025
Search for a Hidden Sector Scalar from Kaon Decay in the Dimuon Final State at ICARUSF Abd Alrahman, P Abratenko, N Abrego-Martinez, et al.
Nature Communications|September 1, 2022
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathwaysWilliam J Young, Najim Lahrouchi, Aaron Isaacs, et al.
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