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N Doan

Showing results (201-210 of 215) with videos related to

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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.
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.
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.
Biorxiv : the Preprint Server for Biology|November 21, 2023
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortexSonia Nan Kim, Vinayak V Viswanadham, Ryan N Doan, et al.
Cell Reports|November 15, 2025
Combined somatic mutation and transcriptome analysis reveals region-specific differences in clonal architecture in human cortexVinayak V Viswanadham, Sonia N Kim, Emre Caglayan, et al.
Cell Stem Cell|February 4, 2018
Inhibition of Methyltransferase Setd7 Allows the In Vitro Expansion of Myogenic Stem Cells with Improved Therapeutic PotentialRobert N Judson, Marco Quarta, Menno J Oudhoff, et al.
Neuron|September 3, 2021
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regionsKelly M Girskis, Andrew B Stergachis, Ellen M DeGennaro, et al.
Pageof 22

Showing results (201-210 of 215) with videos related to

Sort By:
Pageof 22
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.
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.
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.
Biorxiv : the Preprint Server for Biology|November 21, 2023
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortexSonia Nan Kim, Vinayak V Viswanadham, Ryan N Doan, et al.
Cell Reports|November 15, 2025
Combined somatic mutation and transcriptome analysis reveals region-specific differences in clonal architecture in human cortexVinayak V Viswanadham, Sonia N Kim, Emre Caglayan, et al.
Cell Stem Cell|February 4, 2018
Inhibition of Methyltransferase Setd7 Allows the In Vitro Expansion of Myogenic Stem Cells with Improved Therapeutic PotentialRobert N Judson, Marco Quarta, Menno J Oudhoff, et al.
Neuron|September 3, 2021
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regionsKelly M Girskis, Andrew B Stergachis, Ellen M DeGennaro, et al.
Pageof 22