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Patrick Sulem

Showing results (111-120 of 260) with videos related to

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Human Molecular Genetics|January 10, 2014
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinomaSimon N Stacey, Patrick Sulem, Daniel F Gudbjartsson, et al.
Science Advances|June 9, 2023
Sequence variants affecting voice pitch in humansRosa S Gisladottir, Agnar Helgason, Bjarni V Halldorsson, et al.
Nature Genetics|March 26, 2015
Loss-of-function variants in ABCA7 confer risk of Alzheimer's diseaseStacy Steinberg, Hreinn Stefansson, Thorlakur Jonsson, et al.
Nature Genetics|July 24, 2024
The correlation between CpG methylation and gene expression is driven by sequence variantsOlafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, et al.
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.
Pageof 26

Showing results (111-120 of 260) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|January 10, 2014
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinomaSimon N Stacey, Patrick Sulem, Daniel F Gudbjartsson, et al.
Science Advances|June 9, 2023
Sequence variants affecting voice pitch in humansRosa S Gisladottir, Agnar Helgason, Bjarni V Halldorsson, et al.
Nature Genetics|March 26, 2015
Loss-of-function variants in ABCA7 confer risk of Alzheimer's diseaseStacy Steinberg, Hreinn Stefansson, Thorlakur Jonsson, et al.
Nature Genetics|July 24, 2024
The correlation between CpG methylation and gene expression is driven by sequence variantsOlafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson, et al.
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.
Pageof 26