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Developmental Cognitive Neuroscience|February 25, 2025
Longitudinal analysis of the ABCD® studySamuel W Hawes, Andrew K Littlefield, Daniel A Lopez, et al.Bioorganic & Medicinal Chemistry Letters|April 15, 2004
Indoline derivatives as 5-HT(2C) receptor agonistsJ M Bentley, D R Adams, D Bebbington, et al.Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.The Journal of Clinical Investigation|February 9, 2022
Streptococcus pneumoniae colonization associates with impaired adaptive immune responses against SARS-CoV-2Elena Mitsi, Jesús Reiné, Britta C Urban, et al.American Journal of Human Genetics|November 8, 2018
Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental DelayMarie Morimoto, Helen Waller-Evans, Zineb Ammous, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 13, 2015
Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiencyWilliam P Bone, Nicole L Washington, Orion J Buske, et al.Neuroimage|July 5, 2024
Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structureMarlee M Vandewouw, Ami Norris-Brilliant, Anum Rahman, et al.Nature Communications|September 3, 2021
Single allele loss-of-function mutations select and sculpt conditional cooperative networks in breast cancerNathan F Schachter, Jessica R Adams, Patryk Skowron, et al.Brain : a Journal of Neurology|August 20, 2021
Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophyEdgard Verdura, Agustí Rodríguez-Palmero, Valentina Vélez-Santamaria, et al.Msphere|May 29, 2025
Application of a high-resolution melt assay for monitoring SARS-CoV-2 variants in Burkina Faso and KenyaCaitlin Greenland-Bews, Sonal Shah, Morine Achieng, et al.Pageof 251