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Showing results (761-770 of 809) with videos related to

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Nature Communications|September 9, 2024
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Nature Communications|November 13, 2024
Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Annals of Clinical and Translational Neurology|September 17, 2025
Functional Connectivity Associations With Markers of Disease Progression in GRN Pathogenic Variant CarriersTaru M Flagan, Stephanie A Chu, Suvi Häkkinen, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 81

Showing results (761-770 of 809) with videos related to

Sort By:
Pageof 81
Nature Communications|September 9, 2024
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Nature Communications|November 13, 2024
Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Annals of Clinical and Translational Neurology|September 17, 2025
Functional Connectivity Associations With Markers of Disease Progression in GRN Pathogenic Variant CarriersTaru M Flagan, Stephanie A Chu, Suvi Häkkinen, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 81