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Erna V Ivarsdottir

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

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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.
Nature Communications|May 26, 2019
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.
Nature Communications|May 5, 2019
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.
Nature Genetics|October 30, 2024
Gene-based burden tests of rare germline variants identify six cancer susceptibility genesErna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante, et al.
The New England Journal of Medicine|September 2, 2020
Humoral Immune Response to SARS-CoV-2 in IcelandDaniel F Gudbjartsson, Gudmundur L Norddahl, Pall Melsted, et al.
Communications Medicine|July 6, 2023
Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control studyHilma Holm, Erna V Ivarsdottir, Thorhildur Olafsdottir, et al.
Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, 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.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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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.
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.
Nature Communications|May 26, 2019
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.
Nature Communications|May 5, 2019
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.
Nature Genetics|October 30, 2024
Gene-based burden tests of rare germline variants identify six cancer susceptibility genesErna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante, et al.
The New England Journal of Medicine|September 2, 2020
Humoral Immune Response to SARS-CoV-2 in IcelandDaniel F Gudbjartsson, Gudmundur L Norddahl, Pall Melsted, et al.
Communications Medicine|July 6, 2023
Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control studyHilma Holm, Erna V Ivarsdottir, Thorhildur Olafsdottir, et al.
Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, 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.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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