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Doruk Beyter

Showing results (11-20 of 22) with videos related to

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Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, 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.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
JAMA Cardiology|December 27, 2023
Variants at the Interleukin 1 Gene Locus and PericarditisRosa B Thorolfsdottir, Andrea B Jonsdottir, Gardar Sveinbjornsson, et al.
Nature Genetics|October 30, 2024
Gene-based burden tests of rare germline variants identify six cancer susceptibility genesErna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante, et al.
Nature|July 21, 2022
The sequences of 150,119 genomes in the UK BiobankBjarni V Halldorsson, Hannes P Eggertsson, Kristjan H S Moore, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
The New England Journal of Medicine|June 20, 2024
Homozygosity for R47H in <i>TREM2</i> and the Risk of Alzheimer's DiseaseHreinn Stefansson, G Bragi Walters, Gardar Sveinbjornsson, et al.
Nature Communications|July 3, 2023
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, 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.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
JAMA Cardiology|December 27, 2023
Variants at the Interleukin 1 Gene Locus and PericarditisRosa B Thorolfsdottir, Andrea B Jonsdottir, Gardar Sveinbjornsson, et al.
Nature Genetics|October 30, 2024
Gene-based burden tests of rare germline variants identify six cancer susceptibility genesErna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante, et al.
Nature|July 21, 2022
The sequences of 150,119 genomes in the UK BiobankBjarni V Halldorsson, Hannes P Eggertsson, Kristjan H S Moore, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
The New England Journal of Medicine|June 20, 2024
Homozygosity for R47H in <i>TREM2</i> and the Risk of Alzheimer's DiseaseHreinn Stefansson, G Bragi Walters, Gardar Sveinbjornsson, et al.
Nature Communications|July 3, 2023
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Pageof 3