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Sulem

Showing results (171-180 of 323) with videos related to

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Nature|October 4, 2023
Large-scale plasma proteomics comparisons through genetics and disease associationsGrimur Hjorleifsson Eldjarn, Egil Ferkingstad, Sigrun H Lund, et al.
Nature Genetics|January 28, 2014
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetesValgerdur Steinthorsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|June 1, 2022
Genetic architecture of band neutrophil fraction in IcelandGudjon R Oskarsson, Magnus K Magnusson, Asmundur Oddsson, et al.
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|October 8, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigoAstros Th Skuladottir, Gyda Bjornsdottir, Muhammad Sulaman Nawaz, et al.
Nature Communications|February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome geneGudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
European Journal of Preventive Cardiology|September 20, 2022
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysisAnna Helgadottir, Gudmar Thorleifsson, Audunn Snaebjarnarson, et al.
Communications Biology|April 26, 2024
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesisAstros Th Skuladottir, Lilja Stefansdottir, Gisli H Halldorsson, et al.
Nature Genetics|October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levelsPatrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Journal of Cellular and Molecular Medicine|October 17, 2018
Identification of Lynch syndrome risk variants in the Romanian populationPaul D Iordache, Dana Mates, Bjarni Gunnarsson, et al.
Pageof 33

Showing results (171-180 of 323) with videos related to

Sort By:
Pageof 33
Nature|October 4, 2023
Large-scale plasma proteomics comparisons through genetics and disease associationsGrimur Hjorleifsson Eldjarn, Egil Ferkingstad, Sigrun H Lund, et al.
Nature Genetics|January 28, 2014
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetesValgerdur Steinthorsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|June 1, 2022
Genetic architecture of band neutrophil fraction in IcelandGudjon R Oskarsson, Magnus K Magnusson, Asmundur Oddsson, et al.
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|October 8, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigoAstros Th Skuladottir, Gyda Bjornsdottir, Muhammad Sulaman Nawaz, et al.
Nature Communications|February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome geneGudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
European Journal of Preventive Cardiology|September 20, 2022
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysisAnna Helgadottir, Gudmar Thorleifsson, Audunn Snaebjarnarson, et al.
Communications Biology|April 26, 2024
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesisAstros Th Skuladottir, Lilja Stefansdottir, Gisli H Halldorsson, et al.
Nature Genetics|October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levelsPatrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Journal of Cellular and Molecular Medicine|October 17, 2018
Identification of Lynch syndrome risk variants in the Romanian populationPaul D Iordache, Dana Mates, Bjarni Gunnarsson, et al.
Pageof 33