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

Tess Levy

Showing results (31-40 of 40) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 40 results.
American Journal of Medical Genetics. Part A|September 11, 2024
Aortic Root Dilation and Genotype Associations in Phelan-McDermid SyndromeJake Gluckman, Tess Levy, Kate Friedman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant J Brown, Pablo F Cañete, Hao Wang, et al.
American Journal of Medical Genetics. Part A|July 1, 2023
Updated consensus guidelines on the management of Phelan-McDermid syndromeSiddharth Srivastava, Mustafa Sahin, Joseph D Buxbaum, et al.
Nature Medicine|March 30, 2026
Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
American Journal of Human Genetics|October 19, 2025
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
American Journal of Human Genetics|May 17, 2023
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
American Journal of Medical Genetics. Part A|September 11, 2024
Aortic Root Dilation and Genotype Associations in Phelan-McDermid SyndromeJake Gluckman, Tess Levy, Kate Friedman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant J Brown, Pablo F Cañete, Hao Wang, et al.
American Journal of Medical Genetics. Part A|July 1, 2023
Updated consensus guidelines on the management of Phelan-McDermid syndromeSiddharth Srivastava, Mustafa Sahin, Joseph D Buxbaum, et al.
Nature Medicine|March 30, 2026
Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
American Journal of Human Genetics|October 19, 2025
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
American Journal of Human Genetics|May 17, 2023
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
Pageof 4