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Hilma Holm

Showing results (31-40 of 175) 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.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, 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.
Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac DeathGardar Sveinbjornsson, Eva F Olafsdottir, Rosa B Thorolfsdottir, 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.
Nature Communications|October 24, 2020
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture riskIda Surakka, Lars G Fritsche, Wei Zhou, 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.
Pageof 18

Showing results (31-40 of 175) with videos related to

Sort By:
Pageof 18
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.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, 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.
Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac DeathGardar Sveinbjornsson, Eva F Olafsdottir, Rosa B Thorolfsdottir, 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.
Nature Communications|October 24, 2020
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture riskIda Surakka, Lars G Fritsche, Wei Zhou, 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.
Pageof 18