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Nature Communications
|
August 15, 2015
Common and rare variants associated with kidney stones and biochemical traits
Asmundur 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 disease
Gudny A Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, et al.
Nature
|
January 22, 2025
Complete human recombination maps
Gunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Scientific Data
|
May 16, 2015
Sequence variants from whole genome sequencing a large group of Icelanders
Daniel F Gudbjartsson, Patrick Sulem, Hannes Helgason, et al.
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.
Human Molecular Genetics
|
November 27, 2018
Sequence variants associating with urinary biomarkers
Stefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, 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.
Page
of 33
Search research articles
Search
Showing results (71-80 of 322) with videos related to
Sort By:
Page
of 33
Nature Communications
|
August 15, 2015
Common and rare variants associated with kidney stones and biochemical traits
Asmundur 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 disease
Gudny A Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, et al.
Nature
|
January 22, 2025
Complete human recombination maps
Gunnar Palsson, Marteinn T Hardarson, Hakon Jonsson, et al.
Scientific Data
|
May 16, 2015
Sequence variants from whole genome sequencing a large group of Icelanders
Daniel F Gudbjartsson, Patrick Sulem, Hannes Helgason, et al.
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.
Human Molecular Genetics
|
November 27, 2018
Sequence variants associating with urinary biomarkers
Stefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, 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.
Page
of 33