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Med (New York, N.Y.)|July 24, 2024
NanoRanger enables rapid single-base-pair resolution of genomic disordersYingzi Zhang, Chongwei Bi, Seba Nadeef, et al.
Cell Reports|December 1, 2021
Ago1 controls myogenic differentiation by regulating eRNA-mediated CBP-guided epigenome reprogrammingBodor Fallatah, Muhammad Shuaib, Sabir Adroub, et al.
Clinical Genetics|June 17, 2026
An Ancient Founder GDF2 Variant Potentially Causes Semi-Dominant Non-Syndromic Pulmonary Arterial HypertensionAbdullah Aldalaan, Seba Nadeef, Ebtissal Khouj, et al.
Cell|September 8, 2018
Atlas of Circadian Metabolism Reveals System-wide Coordination and Communication between ClocksKenneth A Dyar, Dominik Lutter, Anna Artati, et al.
Genome Medicine|December 15, 2023
Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseasesLama AlAbdi, Hanan E Shamseldin, Ebtissal Khouj, et al.
Med (New York, N.Y.)|November 6, 2024
Arab founder variants: Contributions to clinical genomics and precision medicineLama AlAbdi, Sateesh Maddirevula, Bayan Aljamal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2026
RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohortDena R Matalon, Angela L Duker, Taylor M Arriaga, et al.
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