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Bjarni V Halldorsson

Showing results (21-30 of 80) with videos related to

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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 Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, 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.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, 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.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Nature Structural & Molecular Biology|January 29, 2024
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombinationValgerdur Steinthorsdottir, Bjarni V Halldorsson, Hakon Jonsson, 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|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
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 Genetics|January 8, 2021
Differences between germline genomes of monozygotic twinsHakon Jonsson, Erna Magnusdottir, Hannes P Eggertsson, 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.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, 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.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Current Biology : CB|October 9, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and NamingRosa S Gisladottir, Erna V Ivarsdottir, Agnar Helgason, et al.
Nature Structural & Molecular Biology|January 29, 2024
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombinationValgerdur Steinthorsdottir, Bjarni V Halldorsson, Hakon Jonsson, 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|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Pageof 8