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H Geschwind

Showing results (721-730 of 809) with videos related to

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Nature Genetics|August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genesXueya Zhou, Pamela Feliciano, Chang Shu, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Neurobiology of Aging|December 13, 2023
Neurite-based white matter alterations in MAPT mutation carriers: A multi-shell diffusion MRI study in the ALLFTD consortiumNick Corriveau-Lecavalier, Nirubol Tosakulwong, Timothy G Lesnick, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 17, 2025
Neurodevelopment and neural environment inform Alzheimer's disease age at onset and phenotypeZachary A Miller, Rik Ossenkoppele, Neill R Graff-Radford, et al.
European Journal of Human Genetics : EJHG|June 30, 2018
Primary brain calcification: an international study reporting novel variants and associated phenotypesEliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, et al.
Plos Genetics|September 20, 2008
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisNicola J Rutherford, Yong-Jie Zhang, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Diverse Genomes, Shared Health: Insights from a Health System BiobankRoni Haas, Michael P Margolis, Angela Wei, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 7, 2017
Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseasesMariet Allen, Xue Wang, Jeremy D Burgess, et al.
Science (New York, N.Y.)|December 15, 2018
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorderMichael J Gandal, Pan Zhang, Evi Hadjimichael, et al.
Cell|January 30, 2026
Molecular features of human pathological tau distinguish tauopathy-associated dementiasMukesh Kumar, Christoph N Schlaffner, Shaojun Tang, et al.
Pageof 81

Showing results (721-730 of 809) with videos related to

Sort By:
Pageof 81
Nature Genetics|August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genesXueya Zhou, Pamela Feliciano, Chang Shu, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Neurobiology of Aging|December 13, 2023
Neurite-based white matter alterations in MAPT mutation carriers: A multi-shell diffusion MRI study in the ALLFTD consortiumNick Corriveau-Lecavalier, Nirubol Tosakulwong, Timothy G Lesnick, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 17, 2025
Neurodevelopment and neural environment inform Alzheimer's disease age at onset and phenotypeZachary A Miller, Rik Ossenkoppele, Neill R Graff-Radford, et al.
European Journal of Human Genetics : EJHG|June 30, 2018
Primary brain calcification: an international study reporting novel variants and associated phenotypesEliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, et al.
Plos Genetics|September 20, 2008
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisNicola J Rutherford, Yong-Jie Zhang, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Diverse Genomes, Shared Health: Insights from a Health System BiobankRoni Haas, Michael P Margolis, Angela Wei, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 7, 2017
Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseasesMariet Allen, Xue Wang, Jeremy D Burgess, et al.
Science (New York, N.Y.)|December 15, 2018
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorderMichael J Gandal, Pan Zhang, Evi Hadjimichael, et al.
Cell|January 30, 2026
Molecular features of human pathological tau distinguish tauopathy-associated dementiasMukesh Kumar, Christoph N Schlaffner, Shaojun Tang, et al.
Pageof 81