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Gudny A Arnadottir

Showing results (1-10 of 46) with videos related to

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Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 17, 2021
Unexplained sudden death: next-generation sequencing to the rescue?Gudny A Arnadottir, David O Arnar
Bioinformatics (Oxford, England)|December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellitesSnædis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, et al.
European Heart Journal. Case Reports|February 16, 2026
A frameshift variant in <i>PKP2</i> can be associated with a complex phenotype in sudden cardiac death: a case reportGustav A Davidsson, Gudny A Arnadottir, Gardar Sveinbjornsson, et al.
European Heart Journal|March 30, 2018
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery diseaseAnna Helgadottir, Patrick Sulem, Gudmundur Thorgeirsson, et al.
European Journal of Human Genetics : EJHG|March 12, 2021
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiencyHrafnhildur L Runolfsdottir, John A Sayer, Olafur S Indridason, et al.
Nature Communications|March 22, 2019
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell densityErna V Ivarsdottir, Stefania Benonisdottir, Gudmar Thorleifsson, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
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.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Nature Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 17, 2021
Unexplained sudden death: next-generation sequencing to the rescue?Gudny A Arnadottir, David O Arnar
Bioinformatics (Oxford, England)|December 6, 2019
popSTR2 enables clinical and population-scale genotyping of microsatellitesSnædis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, et al.
European Heart Journal. Case Reports|February 16, 2026
A frameshift variant in <i>PKP2</i> can be associated with a complex phenotype in sudden cardiac death: a case reportGustav A Davidsson, Gudny A Arnadottir, Gardar Sveinbjornsson, et al.
European Heart Journal|March 30, 2018
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery diseaseAnna Helgadottir, Patrick Sulem, Gudmundur Thorgeirsson, et al.
European Journal of Human Genetics : EJHG|March 12, 2021
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiencyHrafnhildur L Runolfsdottir, John A Sayer, Olafur S Indridason, et al.
Nature Communications|March 22, 2019
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell densityErna V Ivarsdottir, Stefania Benonisdottir, Gudmar Thorleifsson, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
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.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Nature Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
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