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

Hildur M Aegisdottir

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
Nature Communications|November 12, 2024
Sequence variants associated with BMI affect disease risk through BMI itselfGudmundur Einarsson, Gudmar Thorleifsson, Valgerdur Steinthorsdottir, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
JAMA Cardiology|September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular PathwaysHildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
European Heart Journal|February 7, 2023
Genetic variants associated with syncope implicate neural and autonomic processesHildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
JAMA Cardiology|December 27, 2023
Variants at the Interleukin 1 Gene Locus and PericarditisRosa B Thorolfsdottir, Andrea B Jonsdottir, Gardar Sveinbjornsson, et al.
European Heart Journal|February 13, 2021
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
Nature Communications|November 12, 2024
Sequence variants associated with BMI affect disease risk through BMI itselfGudmundur Einarsson, Gudmar Thorleifsson, Valgerdur Steinthorsdottir, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
JAMA Cardiology|September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular PathwaysHildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
European Heart Journal|February 7, 2023
Genetic variants associated with syncope implicate neural and autonomic processesHildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
JAMA Cardiology|December 27, 2023
Variants at the Interleukin 1 Gene Locus and PericarditisRosa B Thorolfsdottir, Andrea B Jonsdottir, Gardar Sveinbjornsson, et al.
European Heart Journal|February 13, 2021
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Pageof 2