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Hilma Holm

Showing results (21-30 of 175) with videos related to

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Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, 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.
Nature Genetics|January 12, 2010
Several common variants modulate heart rate, PR interval and QRS durationHilma Holm, Daniel F Gudbjartsson, David O Arnar, 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.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
The Journal of Clinical Endocrinology and Metabolism|December 20, 2023
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral DensityUnnur Styrkarsdottir, Vinicius Tragante, Lilja Stefansdottir, et al.
Plos Genetics|August 6, 2010
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesDaniel F Gudbjartsson, Hilma Holm, Olafur S Indridason, et al.
Journal of the American Heart Association|March 13, 2015
Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the communityBernhard M Kaess, Sarah R Preis, Wolfgang Lieb, 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 Genetics|July 20, 2021
Distinction between the effects of parental and fetal genomes on fetal growthThorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Pageof 18

Showing results (21-30 of 175) with videos related to

Sort By:
Pageof 18
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, 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.
Nature Genetics|January 12, 2010
Several common variants modulate heart rate, PR interval and QRS durationHilma Holm, Daniel F Gudbjartsson, David O Arnar, 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.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
The Journal of Clinical Endocrinology and Metabolism|December 20, 2023
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral DensityUnnur Styrkarsdottir, Vinicius Tragante, Lilja Stefansdottir, et al.
Plos Genetics|August 6, 2010
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesDaniel F Gudbjartsson, Hilma Holm, Olafur S Indridason, et al.
Journal of the American Heart Association|March 13, 2015
Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the communityBernhard M Kaess, Sarah R Preis, Wolfgang Lieb, 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 Genetics|July 20, 2021
Distinction between the effects of parental and fetal genomes on fetal growthThorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, et al.
Pageof 18