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

Dimitrios Vitsios

Showing results (21-30 of 26) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 26 results.
Nature|October 4, 2023
Rare variant associations with plasma protein levels in the UK BiobankRyan S Dhindsa, Oliver S Burren, Benjamin B Sun, et al.
Communications Biology|March 24, 2021
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosisRyan S Dhindsa, Johan Mattsson, Abhishek Nag, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome SequencingKeren J Carss, Anna A Baranowska, Javier Armisen, et al.
Science Advances|November 16, 2022
Human genetics uncovers <i>MAP3K15</i> as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.
NPJ Genomic Medicine|December 10, 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>Charles A Steward, Jolien Roovers, Marie-Marthe Suner, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature|October 4, 2023
Rare variant associations with plasma protein levels in the UK BiobankRyan S Dhindsa, Oliver S Burren, Benjamin B Sun, et al.
Communications Biology|March 24, 2021
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosisRyan S Dhindsa, Johan Mattsson, Abhishek Nag, et al.
Cell Reports|March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's diseaseThomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome SequencingKeren J Carss, Anna A Baranowska, Javier Armisen, et al.
Science Advances|November 16, 2022
Human genetics uncovers <i>MAP3K15</i> as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.
NPJ Genomic Medicine|December 10, 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>Charles A Steward, Jolien Roovers, Marie-Marthe Suner, et al.
Pageof 3