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Erna V Ivarsdottir

Showing results (21-30 of 40) with videos related to

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Communications Biology|April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesisGudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
Nature Communications|July 9, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, et al.
Nature|June 26, 2020
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Thorunn A Olafsdottir, Erna V Ivarsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2024
A partial loss-of-function variant in STAT6 protects against type 2 asthmaKatla Kristjansdottir, Gudmundur L Norddahl, Erna V Ivarsdottir, et al.
European Heart Journal|February 13, 2021
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Communications Biology|April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesisGudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.
Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.
Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.
Nature Communications|July 9, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, et al.
Nature|June 26, 2020
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Thorunn A Olafsdottir, Erna V Ivarsdottir, et al.
European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2024
A partial loss-of-function variant in STAT6 protects against type 2 asthmaKatla Kristjansdottir, Gudmundur L Norddahl, Erna V Ivarsdottir, et al.
European Heart Journal|February 13, 2021
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.
Pageof 4