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

H Geschwind

Showing results (501-510 of 809) with videos related to

Pageof 81
Sort By:
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.
Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.
Neuron|December 12, 2023
Genome-wide study reveals novel roles for formin-2 in axon regeneration as a microtubule dynamics regulator and therapeutic target for nerve repairNgan Pan Bennett Au, Tan Wu, Xinyu Chen, et al.
JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.
Pageof 81

Showing results (501-510 of 809) with videos related to

Sort By:
Pageof 81
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.
Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.
Neuron|December 12, 2023
Genome-wide study reveals novel roles for formin-2 in axon regeneration as a microtubule dynamics regulator and therapeutic target for nerve repairNgan Pan Bennett Au, Tan Wu, Xinyu Chen, et al.
JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.
Pageof 81