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Sulem

Showing results (71-80 of 322) with videos related to

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Nature Communications|August 15, 2015
Common and rare variants associated with kidney stones and biochemical traitsAsmundur Oddsson, Patrick Sulem, Hannes Helgason, et al.
Nature Communications|October 27, 2018
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous diseaseGudny A Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, et al.
Nature|January 22, 2025
Complete human recombination mapsGunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Scientific Data|May 16, 2015
Sequence variants from whole genome sequencing a large group of IcelandersDaniel F Gudbjartsson, Patrick Sulem, Hannes Helgason, et al.
Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Nature Genetics|March 26, 2015
Identification of a large set of rare complete human knockoutsPatrick Sulem, Hannes Helgason, Asmundur Oddson, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2021
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in IcelandUnnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Human Molecular Genetics|August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney diseaseGardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Communications Biology|June 19, 2021
Predicting the probability of death using proteomicsThjodbjorg Eiriksdottir, Steinthor Ardal, Benedikt A Jonsson, et al.
Pageof 33

Showing results (71-80 of 322) with videos related to

Sort By:
Pageof 33
Nature Communications|August 15, 2015
Common and rare variants associated with kidney stones and biochemical traitsAsmundur Oddsson, Patrick Sulem, Hannes Helgason, et al.
Nature Communications|October 27, 2018
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous diseaseGudny A Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, et al.
Nature|January 22, 2025
Complete human recombination mapsGunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Scientific Data|May 16, 2015
Sequence variants from whole genome sequencing a large group of IcelandersDaniel F Gudbjartsson, Patrick Sulem, Hannes Helgason, et al.
Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Nature Genetics|March 26, 2015
Identification of a large set of rare complete human knockoutsPatrick Sulem, Hannes Helgason, Asmundur Oddson, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2021
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in IcelandUnnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Human Molecular Genetics|August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney diseaseGardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Communications Biology|June 19, 2021
Predicting the probability of death using proteomicsThjodbjorg Eiriksdottir, Steinthor Ardal, Benedikt A Jonsson, et al.
Pageof 33