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Sulem

Showing results (191-200 of 323) with videos related to

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Nature Communications|September 9, 2018
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traitsThorunn Rafnar, Bjarni Gunnarsson, Olafur A Stefansson, et al.
Communications Biology|April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesisGudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Cancer Research|February 19, 2021
Loss-of-Function Variants in the Tumor-Suppressor Gene <i>PTPN14</i> Confer Increased Cancer RiskThorhildur Olafsdottir, Simon N Stacey, Gardar Sveinbjornsson, et al.
Nature Genetics|September 17, 2013
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degenerationHannes Helgason, Patrick Sulem, Maheswara R Duvvari, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Plos Genetics|June 14, 2012
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesRui Li, Felix F Brockschmidt, Amy K Kiefer, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Plos Genetics|March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthmaDirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Pageof 33

Showing results (191-200 of 323) with videos related to

Sort By:
Pageof 33
Nature Communications|September 9, 2018
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traitsThorunn Rafnar, Bjarni Gunnarsson, Olafur A Stefansson, et al.
Communications Biology|April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesisGudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Cancer Research|February 19, 2021
Loss-of-Function Variants in the Tumor-Suppressor Gene <i>PTPN14</i> Confer Increased Cancer RiskThorhildur Olafsdottir, Simon N Stacey, Gardar Sveinbjornsson, et al.
Nature Genetics|September 17, 2013
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degenerationHannes Helgason, Patrick Sulem, Maheswara R Duvvari, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Plos Genetics|June 14, 2012
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesRui Li, Felix F Brockschmidt, Amy K Kiefer, et al.
Human Molecular Genetics|December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibitionRosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Plos Genetics|March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthmaDirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Pageof 33