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Nature Genetics
|
March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genome
Birte Kehr, Anna Helgadottir, Pall Melsted, et al.
Nature Genetics
|
March 26, 2015
Identification of a large set of rare complete human knockouts
Patrick 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 Iceland
Unnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Human Molecular Genetics
|
August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney disease
Gardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Communications Biology
|
June 19, 2021
Predicting the probability of death using proteomics
Thjodbjorg 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 SNPs
Hongping 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 Fibrillation
Rosa 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 heritability
Erna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Nature Genetics
|
April 19, 2016
Physical and neurobehavioral determinants of reproductive onset and success
Felix 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 syndrome
Elin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson, et al.
Page
of 28
Search research articles
Search
Showing results (31-40 of 280) with videos related to
Sort By:
Page
of 28
Nature Genetics
|
March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genome
Birte Kehr, Anna Helgadottir, Pall Melsted, et al.
Nature Genetics
|
March 26, 2015
Identification of a large set of rare complete human knockouts
Patrick 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 Iceland
Unnur Styrkarsdottir, Sigrun H Lund, Saedis Saevarsdottir, et al.
Human Molecular Genetics
|
August 2, 2014
Rare mutations associating with serum creatinine and chronic kidney disease
Gardar Sveinbjornsson, Evgenia Mikaelsdottir, Runolfur Palsson, et al.
Communications Biology
|
June 19, 2021
Predicting the probability of death using proteomics
Thjodbjorg 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 SNPs
Hongping 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 Fibrillation
Rosa 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 heritability
Erna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
Nature Genetics
|
April 19, 2016
Physical and neurobehavioral determinants of reproductive onset and success
Felix 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 syndrome
Elin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson, et al.
Page
of 28