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 (81-90 of 144) with videos related to

Pageof 15
Sort By:
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Nature Genetics|January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitisRagnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.
Plos One|June 8, 2010
Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studiesKatherine S Elliott, Eleftheria Zeggini, Mark I McCarthy, et al.
Nature Communications|April 10, 2015
New basal cell carcinoma susceptibility lociSimon N Stacey, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Nature Communications|July 9, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, et al.
Nature Communications|February 15, 2017
A genome-wide association study yields five novel thyroid cancer risk lociJulius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, et al.
Nature Genetics|October 14, 2008
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSimon N Stacey, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.
Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.
Pageof 15

Showing results (81-90 of 144) with videos related to

Sort By:
Pageof 15
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Nature Genetics|January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitisRagnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.
Plos One|June 8, 2010
Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studiesKatherine S Elliott, Eleftheria Zeggini, Mark I McCarthy, et al.
Nature Communications|April 10, 2015
New basal cell carcinoma susceptibility lociSimon N Stacey, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Nature Communications|July 9, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, et al.
Nature Communications|February 15, 2017
A genome-wide association study yields five novel thyroid cancer risk lociJulius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, et al.
Nature Genetics|October 14, 2008
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSimon N Stacey, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.
Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.
The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.
Pageof 15