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Erna V Ivarsdottir

Showing results (1-10 of 40) with videos related to

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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.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2021
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in IcelandUnnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Communications Biology|June 19, 2021
Predicting the probability of death using proteomicsThjodbjorg Eiriksdottir, Steinthor Ardal, Benedikt A Jonsson, 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|July 20, 2021
Distinction between the effects of parental and fetal genomes on fetal growthThorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, 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.
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.
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.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, 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.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
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.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2021
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in IcelandUnnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Communications Biology|June 19, 2021
Predicting the probability of death using proteomicsThjodbjorg Eiriksdottir, Steinthor Ardal, Benedikt A Jonsson, 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|July 20, 2021
Distinction between the effects of parental and fetal genomes on fetal growthThorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, 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.
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.
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.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, 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.
Pageof 4