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 (11-20 of 65) with videos related to

Pageof 7
Sort By:
Science (New York, N.Y.)|January 26, 2019
Characterizing mutagenic effects of recombination through a sequence-level genetic mapBjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Nature Communications|June 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
Nature Genetics|October 24, 2018
Insights into imprinting from parent-of-origin phased methylomes and transcriptomesFlorian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, et al.
Blood Cancer Journal|April 20, 2021
Germline variants at SOHLH2 influence multiple myeloma riskLaura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Brain Communications|November 23, 2022
Thirty novel sequence variants impacting human intracranial volumeMuhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, et al.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Science (New York, N.Y.)|January 26, 2019
Characterizing mutagenic effects of recombination through a sequence-level genetic mapBjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, et al.
Nature Communications|June 29, 2023
Sequence variants affecting the genome-wide rate of germline microsatellite mutationsSnaedis Kristmundsdottir, Hakon Jonsson, Marteinn T Hardarson, et al.
Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Nature Communications|June 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
Nature Genetics|October 24, 2018
Insights into imprinting from parent-of-origin phased methylomes and transcriptomesFlorian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, et al.
Blood Cancer Journal|April 20, 2021
Germline variants at SOHLH2 influence multiple myeloma riskLaura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Brain Communications|November 23, 2022
Thirty novel sequence variants impacting human intracranial volumeMuhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, et al.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Pageof 7