Search Results - "Sveinbjornsson, Gardar"

A Missense Variant in PLEC Increases Risk of Atrial Fibrillation.

Authors: Thorolfsdottir, Rosa B. Sveinbjornsson, Gardar Sulem, Patrick et al.

Source: Journal of the American College of Cardiology (JACC). Oct2017, Vol. 70 Issue 17, p2157-2168. 12p.

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood.

Authors: Olafsson, Sigurgeir Alexandersson, Kristjan F. Gizurarson, Johann G. K. et al.

Source: Cancer Epidemiology, Biomarkers & Prevention. Jan2020, Vol. 29 Issue 1, p225-235.

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Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.

Authors: Thorolfsdottir, Rosa B. Sveinbjornsson, Gardar Sulem, Patrick et al.

Source: Communications Biology. 12/1/2018, Vol. 1 Issue 1, pN.PAG-N.PAG. 1p.

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Abstract 15122: Use of Genetic Information in Attempt to Modify the Risk of Sudden Cardiac Death by Screening the Icelandic Population for Variants Associating With the Long QT-Syndrome.

Authors: Benediktsdottir, Bára D Sveinbjornsson, Gardar Sigfússon, Gunnlaugur et al.

Source: Circulation. 2018 Supplement, Vol. 138, pA15122-A15122. 1p.

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.

Authors: Kristjansson, Ragnar P. Oskarsson, Gudjon R. Skuladottir, Astros et al.

Source: Communications Biology. 7/10/2023, Vol. 6 Issue 1, p1-9. 9p.

Genetic architecture of band neutrophil fraction in Iceland.

Authors: Oskarsson, Gudjon R. Magnusson, Magnus K. Oddsson, Asmundur et al.

Source: Communications Biology. 6/1/2022, Vol. 5 Issue 1, p1-11. 11p.

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.

Authors: Ivarsdottir, Erna V. Holm, Hilma Benonisdottir, Stefania et al.

Source: Communications Biology. 6/9/2021, Vol. 4 Issue 1, p1-13. 13p.

A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.

Authors: Skuladottir, Astros Th. Bjornsdottir, Gyda Thorleifsson, Gudmar et al.

Source: Scientific Reports. 2/18/2021, Vol. 11 Issue 1, p1-8. 8p.

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.

Authors: Oskarsson, Gudjon R. Oddsson, Asmundur Magnusson, Magnus K. et al.

Source: Communications Biology. 4/23/2020, Vol. 3 Issue 1, p1-10. 10p.

A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin.

Authors: Oskarsson, Gudjon R. Kristjansson, Ragnar P. Lee, Amy L. et al.

Source: Communications Biology. 12/1/2018, Vol. 1 Issue 1, pN.PAG-N.PAG. 1p.

A frameshift variant in PKP2 can be associated with a complex phenotype in sudden cardiac death: a case report.

Authors: Davidsson GA Arnadottir GA Sveinbjornsson G et al.

Source: European heart journal. Case reports [Eur Heart J Case Rep] 2026 Jan 29; Vol. 10 (2), pp. ytag067. Date of Electronic Publication: 2026 Jan 29 (Print Publication: 2026).

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 101730741 Publication Model: eCollection Cited Medium: Internet ISSN: 2514-2119 (Electronic) Linking ISSN: 25142119 NLM ISO Abbreviation: Eur Heart J Case Rep Subsets: PubMed not MEDLINE

Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition.

Authors: Thorolfsdottir RB Sveinbjornsson G Hjorleifsson Eldjarn G et al.

Corporate Authors: Thorolfsdottir RB Sveinbjornsson G Hjorleifsson Eldjarn G et al.

Source: Human molecular genetics [Hum Mol Genet] 2026 Feb 09; Vol. 35 (2).

Publication Type: Journal Article

Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Missense variants in FRS3 affect body mass index in populations of diverse ancestries.

Authors: Jonsdottir AB Sveinbjornsson G Thorolfsdottir RB et al.

Corporate Authors: Jonsdottir AB Sveinbjornsson G Thorolfsdottir RB et al.

Source: Nature communications [Nat Commun] 2025 Mar 25; Vol. 16 (1), pp. 2694. Date of Electronic Publication: 2025 Mar 25.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Sequence variants associated with BMI affect disease risk through BMI itself.

Authors: Einarsson G Thorleifsson G Steinthorsdottir V et al.

Source: Nature communications [Nat Commun] 2024 Nov 12; Vol. 15 (1), pp. 9335. Date of Electronic Publication: 2024 Nov 12.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction.

Authors: Small AM Yang TY Itoh S et al.

Corporate Authors: Small AM Yang TY Itoh S et al.

Source: Nature genetics [Nat Genet] 2026 Jan; Vol. 58 (1), pp. 57-66. Date of Electronic Publication: 2025 Dec 19.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication.

Authors: Einarsson G Arnason HK Gisladottir RS et al.

Source: Biological psychiatry global open science [Biol Psychiatry Glob Open Sci] 2025 Nov 10; Vol. 6 (2), pp. 100652. Date of Electronic Publication: 2025 Nov 10 (Print Publication: 2026).

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Inc. on behalf of Society of Biological Psychiatry Country of Publication: United States NLM ID: 9918227369306676 Publication Model: eCollection Cited Medium: Internet ISSN: 2667-1743 (Electronic) Linking ISSN: 26671743 NLM ISO Abbreviation: Biol Psychiatry Glob Open Sci Subsets: PubMed not MEDLINE

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Authors: Skuladottir AT Tragante V Sveinbjornsson G et al.

Source: NPJ Parkinson's disease [NPJ Parkinsons Dis] 2024 Aug 15; Vol. 10 (1), pp. 140. Date of Electronic Publication: 2024 Aug 15.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 101675390 Publication Model: Electronic Cited Medium: Print ISSN: 2373-8057 (Print) Linking ISSN: 23738057 NLM ISO Abbreviation: NPJ Parkinsons Dis Subsets: PubMed not MEDLINE