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Nature Communications
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January 22, 2020
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Thorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, et al.
Nature Genetics
|
January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Nature Genetics
|
June 20, 2017
Identification of sequence variants influencing immunoglobulin levels
Stefan Jonsson, Gardar Sveinbjornsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Human Molecular Genetics
|
November 27, 2018
Sequence variants associating with urinary biomarkers
Stefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Communications Biology
|
April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Gudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Plos Genetics
|
March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma
Dirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Communications
|
September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levels
Thorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
European Heart Journal
|
July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
Anna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Nature Communications
|
March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosis
Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
Nature Genetics
|
January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Ragnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.
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of 11
Search research articles
Search
Showing results (61-70 of 102) with videos related to
Sort By:
Page
of 11
Nature Communications
|
January 22, 2020
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Thorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, et al.
Nature Genetics
|
January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Nature Genetics
|
June 20, 2017
Identification of sequence variants influencing immunoglobulin levels
Stefan Jonsson, Gardar Sveinbjornsson, Aitzkoa Lopez de Lapuente Portilla, et al.
Human Molecular Genetics
|
November 27, 2018
Sequence variants associating with urinary biomarkers
Stefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Communications Biology
|
April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Gudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Plos Genetics
|
March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma
Dirk Smith, Hannes Helgason, Patrick Sulem, et al.
Nature Communications
|
September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levels
Thorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.
European Heart Journal
|
July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
Anna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Nature Communications
|
March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosis
Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
Nature Genetics
|
January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Ragnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.
Page
of 11