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Sulem

Showing results (101-110 of 322) with videos related to

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Genome Medicine|April 14, 2025
Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomaliesFrancesca Mattioli, Rún Friðriksdóttir, Anne Hebert, et al.
Carcinogenesis|February 5, 2011
Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association studySheng Wei, Jiangong Niu, Hui Zhao, et al.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, et al.
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, 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.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, et al.
Nature Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
Pageof 33

Showing results (101-110 of 322) with videos related to

Sort By:
Pageof 33
Genome Medicine|April 14, 2025
Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomaliesFrancesca Mattioli, Rún Friðriksdóttir, Anne Hebert, et al.
Carcinogenesis|February 5, 2011
Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association studySheng Wei, Jiangong Niu, Hui Zhao, et al.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, et al.
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, 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.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, et al.
Nature Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, et al.
Pageof 33