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Ragnar P Kristjansson

Showing results (1-10 of 22) with videos related to

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BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Communications Biology|May 27, 2024
Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood DonorsIsa Amalie Olofsson, Ragnar P Kristjansson, Ida Callesen, 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.
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.
Scientific Reports|June 10, 2017
Sequence variant at 4q25 near PITX2 associates with appendicitisRagnar P Kristjansson, Stefania Benonisdottir, Asmundur Oddsson, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, 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 Communications|November 17, 2016
Epigenetic and genetic components of height regulationStefania Benonisdottir, Asmundur Oddsson, Agnar Helgason, et al.
Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Communications Biology|May 27, 2024
Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood DonorsIsa Amalie Olofsson, Ragnar P Kristjansson, Ida Callesen, 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.
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.
Scientific Reports|June 10, 2017
Sequence variant at 4q25 near PITX2 associates with appendicitisRagnar P Kristjansson, Stefania Benonisdottir, Asmundur Oddsson, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, 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 Communications|November 17, 2016
Epigenetic and genetic components of height regulationStefania Benonisdottir, Asmundur Oddsson, Agnar Helgason, et al.
Nature Genetics|May 11, 2021
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsDoruk Beyter, Helga Ingimundardottir, Asmundur Oddsson, et al.
Pageof 3