Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Daniel Geschwind

Showing results (41-50 of 67) with videos related to

Pageof 7
Sort By:
Biorxiv : the Preprint Server for Biology|April 1, 2025
Structural Determinants of Signal Speed: A Multimodal Investigation of Face Processing in Autism Spectrum DisorderCampbell R Coleman, Madelyn G Nance, Zachary Jacokes, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Brain : a Journal of Neurology|June 22, 2022
Right temporal degeneration and socioemotional semantics: semantic behavioural variant frontotemporal dementiaKyan Younes, Valentina Borghesani, Maxime Montembeault, et al.
Neuron|May 17, 2016
Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression SusceptibilityRosemary C Bagot, Hannah M Cates, Immanuel Purushothaman, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Nature|May 31, 2023
Myelin dysfunction drives amyloid-β deposition in models of Alzheimer's diseaseConstanze Depp, Ting Sun, Andrew Octavian Sasmita, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
JAMA Neurology|June 22, 2026
Clinical Associations of Cerebrospinal Fluid TMEM106B in Familial and Sporadic Frontotemporal DementiaMolly Olzinski, Joshua Downer, Yann Cobigo, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Biorxiv : the Preprint Server for Biology|April 1, 2025
Structural Determinants of Signal Speed: A Multimodal Investigation of Face Processing in Autism Spectrum DisorderCampbell R Coleman, Madelyn G Nance, Zachary Jacokes, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Brain : a Journal of Neurology|June 22, 2022
Right temporal degeneration and socioemotional semantics: semantic behavioural variant frontotemporal dementiaKyan Younes, Valentina Borghesani, Maxime Montembeault, et al.
Neuron|May 17, 2016
Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression SusceptibilityRosemary C Bagot, Hannah M Cates, Immanuel Purushothaman, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Nature|May 31, 2023
Myelin dysfunction drives amyloid-β deposition in models of Alzheimer's diseaseConstanze Depp, Ting Sun, Andrew Octavian Sasmita, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
JAMA Neurology|June 22, 2026
Clinical Associations of Cerebrospinal Fluid TMEM106B in Familial and Sporadic Frontotemporal DementiaMolly Olzinski, Joshua Downer, Yann Cobigo, et al.
Pageof 7