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Hannes Helgason

Showing results (41-50 of 54) with videos related to

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Human Molecular Genetics|January 8, 2016
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancerSimon N Stacey, Birte Kehr, Julius Gudmundsson, et al.
Nature Genetics|March 26, 2015
Large-scale whole-genome sequencing of the Icelandic populationDaniel F Gudbjartsson, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Nature Genetics|March 21, 2017
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritisUnnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, et al.
Nature Genetics|July 28, 2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritisUnnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, et al.
The New England Journal of Medicine|May 19, 2016
Variant ASGR1 Associated with a Reduced Risk of Coronary Artery DiseasePaul Nioi, Asgeir Sigurdsson, Gudmar Thorleifsson, 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.
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.
Human Molecular Genetics|May 28, 2014
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancerThorunn Rafnar, Patrick Sulem, Gudmar Thorleifsson, 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.
Nature Communications|June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|January 8, 2016
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancerSimon N Stacey, Birte Kehr, Julius Gudmundsson, et al.
Nature Genetics|March 26, 2015
Large-scale whole-genome sequencing of the Icelandic populationDaniel F Gudbjartsson, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Nature Genetics|March 21, 2017
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritisUnnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, et al.
Nature Genetics|July 28, 2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritisUnnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, et al.
The New England Journal of Medicine|May 19, 2016
Variant ASGR1 Associated with a Reduced Risk of Coronary Artery DiseasePaul Nioi, Asgeir Sigurdsson, Gudmar Thorleifsson, 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.
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.
Human Molecular Genetics|May 28, 2014
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancerThorunn Rafnar, Patrick Sulem, Gudmar Thorleifsson, 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.
Nature Communications|June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.
Pageof 6