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Hannes Helgason

Showing results (11-20 of 54) with videos related to

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European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, 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.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Plos Genetics|September 2, 2015
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery DiseaseSolveig Gretarsdottir, Hannes Helgason, Anna Helgadottir, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Nature Genetics|March 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorderThorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|November 14, 2013
A common variant at 8q24.21 is associated with renal cell cancerJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, 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.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Plos Genetics|September 2, 2015
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery DiseaseSolveig Gretarsdottir, Hannes Helgason, Anna Helgadottir, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Nature Genetics|March 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorderThorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|November 14, 2013
A common variant at 8q24.21 is associated with renal cell cancerJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.
Pageof 6