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Cancer Discovery|August 14, 2021
Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human BrainJavier Ganz, Eduardo A Maury, Basheer Becerra, et al.Veterinary Pathology|September 7, 2021
Pathologic characterization of canine multiple system degeneration in the Ibizan houndSamantha C St Jean, Bernard S Jortner, Ryan N Doan, et al.Cell|September 27, 2016
Mutations in Human Accelerated Regions Disrupt Cognition and Social BehaviorRyan N Doan, Byoung-Il Bae, Beatriz Cubelos, et al.Biorxiv : the Preprint Server for Biology|July 9, 2024
Neuropathologically-directed profiling of PRNP somatic and germline variants in sporadic human prion diseaseGannon A McDonough, Yuchen Cheng, Katherine Morillo, et al.Acta Neuropathologica|July 24, 2024
Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion diseaseGannon A McDonough, Yuchen Cheng, Katherine S Morillo, et al.Nature Genetics|June 19, 2019
Recessive gene disruptions in autism spectrum disorderRyan N Doan, Elaine T Lim, Silvia De Rubeis, et al.Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.Nature Neuroscience|January 12, 2021
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.Cell Genomics|July 17, 2024
Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.Pageof 3