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

Colin P Doherty

Showing results (111-120 of 114) with videos related to

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 114 results.
Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)|March 21, 2020
The genetic architecture of the human cerebral cortexKatrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
Pageof 12

Showing results (111-120 of 114) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 114 results.
Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)|March 21, 2020
The genetic architecture of the human cerebral cortexKatrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
Pageof 12