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Gisli Masson

Showing results (21-30 of 119) with videos related to

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Nature|August 24, 2012
Rate of de novo mutations and the importance of father's age to disease riskAugustine Kong, Michael L Frigge, Gisli Masson, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
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.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, 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.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, 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 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
Nature Communications|February 23, 2017
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniationGyda Bjornsdottir, Stefania Benonisdottir, Gardar Sveinbjornsson, et al.
Pageof 12

Showing results (21-30 of 119) with videos related to

Sort By:
Pageof 12
Nature|August 24, 2012
Rate of de novo mutations and the importance of father's age to disease riskAugustine Kong, Michael L Frigge, Gisli Masson, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
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.
Blood|May 10, 2017
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderlyFlorian Zink, Simon N Stacey, Gudmundur L Norddahl, 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.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, 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 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
Nature Communications|February 23, 2017
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniationGyda Bjornsdottir, Stefania Benonisdottir, Gardar Sveinbjornsson, et al.
Pageof 12