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JAMA Network Open|November 22, 2023
Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-AnalysisAna B W Greenberg, Neel H Mehta, Garrett Allington, et al.STAR Protocols|March 22, 2021
Analysis workflow to assess de novo genetic variants from human whole-exome sequencingNicholas S Diab, Spencer King, Weilai Dong, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 14, 2016
Alzheimer's disease-associated TREM2 variants exhibit either decreased or increased ligand-dependent activationWilbur Song, Basavaraj Hooli, Kristina Mullin, et al.Genes|July 2, 2021
Molecular Genetics and Complex Inheritance of Congenital Heart DiseaseNicholas S Diab, Syndi Barish, Weilai Dong, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 7, 2021
Genomics of human congenital hydrocephalusAdam J Kundishora, Amrita K Singh, Garrett Allington, et al.Elife|June 6, 2022
Quantifying concordant genetic effects of de novo mutations on multiple disordersHanmin Guo, Lin Hou, Yu Shi, et al.Frontiers in Neurology|February 8, 2021
Insights From Genetic Studies of Cerebral PalsySara A Lewis, Sheetal Shetty, Bryce A Wilson, et al.Cerebral Cortex (New York, N.Y. : 1991)|July 19, 2022
Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesisHanya M Qureshi, Kedous Y Mekbib, Garrett Allington, et al.Journal of Neuroinflammation|May 23, 2025
Diverse cell types establish a pathogenic immune environment in peripheral neuropathyJulie Choi, Amy Strickland, Hui Qi Loo, et al.Clinical Genetics|April 27, 2021
Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelinationSalma Omer, Sheng Chih Jin, Rainelli Koumangoye, et al.Pageof 10