Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Thorunn Rafnar

Showing results (71-80 of 144) with videos related to

Pageof 15
Sort By:
Cancer Research|February 10, 2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer riskThorunn Rafnar, Patrick Sulem, Soren Besenbacher, et al.
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.
Nature Communications|January 11, 2022
Functional dissection of inherited non-coding variation influencing multiple myeloma riskRam Ajore, Abhishek Niroula, Maroulio Pertesi, et al.
Nature Genetics|May 20, 2008
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinomaDaniel F Gudbjartsson, Patrick Sulem, Simon N Stacey, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, 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.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Nature Genetics|February 10, 2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, 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.
Pageof 15

Showing results (71-80 of 144) with videos related to

Sort By:
Pageof 15
Cancer Research|February 10, 2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer riskThorunn Rafnar, Patrick Sulem, Soren Besenbacher, et al.
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.
Nature Communications|January 11, 2022
Functional dissection of inherited non-coding variation influencing multiple myeloma riskRam Ajore, Abhishek Niroula, Maroulio Pertesi, et al.
Nature Genetics|May 20, 2008
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinomaDaniel F Gudbjartsson, Patrick Sulem, Simon N Stacey, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, 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.
Nature Genetics|April 9, 2008
Many sequence variants affecting diversity of adult human heightDaniel F Gudbjartsson, G Bragi Walters, Gudmar Thorleifsson, et al.
Nature Genetics|February 10, 2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, 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.
Pageof 15