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Patrick Sulem

Showing results (31-40 of 280) with videos related to

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Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, 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.
DNA Repair|February 8, 2011
An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPsHongping Yu, Hui Zhao, Li-E Wang, et al.
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Nature Genetics|April 19, 2016
Physical and neurobehavioral determinants of reproductive onset and successFelix R Day, Hannes Helgason, Daniel I Chasman, et al.
European Journal of Human Genetics : EJHG|September 8, 2023
A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndromeElin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson, et al.
Pageof 28

Showing results (31-40 of 280) with videos related to

Sort By:
Pageof 28
Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, 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.
DNA Repair|February 8, 2011
An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPsHongping Yu, Hui Zhao, Li-E Wang, et al.
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Nature Genetics|April 19, 2016
Physical and neurobehavioral determinants of reproductive onset and successFelix R Day, Hannes Helgason, Daniel I Chasman, et al.
European Journal of Human Genetics : EJHG|September 8, 2023
A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndromeElin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson, et al.
Pageof 28