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

G Bragi Walters

Showing results (41-50 of 87) with videos related to

Pageof 9
Sort By:
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|October 8, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigoAstros Th Skuladottir, Gyda Bjornsdottir, Muhammad Sulaman Nawaz, et al.
Scientific Reports|February 19, 2021
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsyAstros Th Skuladottir, Gyda Bjornsdottir, Gudmar Thorleifsson, et al.
Communications Biology|April 26, 2024
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesisAstros Th Skuladottir, Lilja Stefansdottir, Gisli H Halldorsson, et al.
Nature|March 18, 2008
Genetics of gene expression and its effect on diseaseValur Emilsson, Gudmar Thorleifsson, Bin Zhang, et al.
Nature Genetics|October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levelsPatrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Nature Genetics|December 17, 2008
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesityGudmar Thorleifsson, G Bragi Walters, Daniel F Gudbjartsson, 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|May 21, 2025
Sequence diversity lost in early pregnancyGudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig, et al.
Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:
Pageof 9
Nature|May 7, 2013
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsUnnur Styrkarsdottir, Gudmar Thorleifsson, Patrick Sulem, et al.
Communications Biology|October 8, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigoAstros Th Skuladottir, Gyda Bjornsdottir, Muhammad Sulaman Nawaz, et al.
Scientific Reports|February 19, 2021
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsyAstros Th Skuladottir, Gyda Bjornsdottir, Gudmar Thorleifsson, et al.
Communications Biology|April 26, 2024
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesisAstros Th Skuladottir, Lilja Stefansdottir, Gisli H Halldorsson, et al.
Nature|March 18, 2008
Genetics of gene expression and its effect on diseaseValur Emilsson, Gudmar Thorleifsson, Bin Zhang, et al.
Nature Genetics|October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levelsPatrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Nature Genetics|December 17, 2008
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesityGudmar Thorleifsson, G Bragi Walters, Daniel F Gudbjartsson, 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|May 21, 2025
Sequence diversity lost in early pregnancyGudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig, et al.
Pageof 9