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Isleifur Olafsson

Showing results (21-30 of 102) with videos related to

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Laeknabladid|July 5, 2006
[Foodborne infections in Iceland. Relationship to allergy and lung function]Hulda Asbjoernsdóttir, Rúna B Sigurjónsd Ttir, Signý V Sveinsd Ttir, et al.
The European Respiratory Journal|May 17, 2014
Obstructive sleep apnoea treatment and fasting lipids: a comparative effectiveness studyBrendan T Keenan, Greg Maislin, Bernie Y Sunwoo, et al.
Blood Cancer Journal|April 8, 2026
Dietary intake and the risk of monoclonal gammopathy of undetermined significance: results from the population-based iStopMM screening studyStyrmir Hallsson, Ingibjorg Gunnarsdottir, Marianna Thordardottir, 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.
Nature Communications|August 15, 2015
Common and rare variants associated with kidney stones and biochemical traitsAsmundur Oddsson, Patrick Sulem, Hannes Helgason, et al.
Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, et al.
Human Molecular Genetics|August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney diseaseGardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Hemasphere|November 20, 2024
Monoclonal gammopathy of undetermined significance with multiple paraproteins: A population-based screening studySæmundur Rögnvaldsson, Jón Þ Óskarsson, Sigrun Thorsteinsdóttir, 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.
Pageof 11

Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Laeknabladid|July 5, 2006
[Foodborne infections in Iceland. Relationship to allergy and lung function]Hulda Asbjoernsdóttir, Rúna B Sigurjónsd Ttir, Signý V Sveinsd Ttir, et al.
The European Respiratory Journal|May 17, 2014
Obstructive sleep apnoea treatment and fasting lipids: a comparative effectiveness studyBrendan T Keenan, Greg Maislin, Bernie Y Sunwoo, et al.
Blood Cancer Journal|April 8, 2026
Dietary intake and the risk of monoclonal gammopathy of undetermined significance: results from the population-based iStopMM screening studyStyrmir Hallsson, Ingibjorg Gunnarsdottir, Marianna Thordardottir, 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.
Nature Communications|August 15, 2015
Common and rare variants associated with kidney stones and biochemical traitsAsmundur Oddsson, Patrick Sulem, Hannes Helgason, et al.
Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, et al.
Human Molecular Genetics|August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney diseaseGardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Hemasphere|November 20, 2024
Monoclonal gammopathy of undetermined significance with multiple paraproteins: A population-based screening studySæmundur Rögnvaldsson, Jón Þ Óskarsson, Sigrun Thorsteinsdóttir, 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.
Pageof 11