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

Evan H Baugh

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Molecular Psychiatry|November 20, 2021
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disordersAnna Alkelai, Lior Greenbaum, Anna R Docherty, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approachAnna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disordersHalie J May, Jaehoon Jeong, Anya Revah-Politi, et al.
Annals of Neurology|April 22, 2018
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsyMelodie R Winawer, Nicole G Griffin, Jorge Samanamud, et al.
Annals of Neurology|October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypesMaureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
American Journal of Human Genetics|January 20, 2022
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorderSébastien Küry, Frédéric Ebstein, Alice Mollé, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Molecular Psychiatry|November 20, 2021
The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disordersAnna Alkelai, Lior Greenbaum, Anna R Docherty, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approachAnna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disordersHalie J May, Jaehoon Jeong, Anya Revah-Politi, et al.
Annals of Neurology|April 22, 2018
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsyMelodie R Winawer, Nicole G Griffin, Jorge Samanamud, et al.
Annals of Neurology|October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypesMaureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
American Journal of Human Genetics|January 20, 2022
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorderSébastien Küry, Frédéric Ebstein, Alice Mollé, et al.
Pageof 2