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

H Halldorsson

Showing results (31-40 of 65) with videos related to

Pageof 7
Sort By:
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 1, 2019
Common and Rare Sequence Variants Influencing Tumor Biomarkers in BloodSigurgeir Olafsson, Kristjan F Alexandersson, Johann G K Gizurarson, 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|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Nature Communications|January 22, 2020
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesisThorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, 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.
Nature Communications|September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levelsThorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, 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 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.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 1, 2019
Common and Rare Sequence Variants Influencing Tumor Biomarkers in BloodSigurgeir Olafsson, Kristjan F Alexandersson, Johann G K Gizurarson, 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|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Nature Communications|January 22, 2020
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesisThorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, 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.
Nature Communications|September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levelsThorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, 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 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.
Pageof 7