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European Heart Journal
|
February 7, 2023
Genetic variants associated with syncope implicate neural and autonomic processes
Hildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
JAMA Cardiology
|
December 27, 2023
Variants at the Interleukin 1 Gene Locus and Pericarditis
Rosa 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 fractures
Unnur 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 fractures
Unnur 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 genes
Erna 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 Iceland
Daniel 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 study
Hilma 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 ancestries
Andrea 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 cardiomyopathy
Michele 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 cardiomyopathy
Michele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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Search research articles
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Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 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 processes
Hildur M Aegisdottir, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
JAMA Cardiology
|
December 27, 2023
Variants at the Interleukin 1 Gene Locus and Pericarditis
Rosa 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 fractures
Unnur 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 fractures
Unnur 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 genes
Erna 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 Iceland
Daniel 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 study
Hilma 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 ancestries
Andrea 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 cardiomyopathy
Michele 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 cardiomyopathy
Michele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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of 4