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  • Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
    By:
    • Bjornsdottir, Gyda;
    • Stefansdottir, Lilja;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Norland, Kristjan;
    • Ferkingstad, Egil;
    • Oddsson, Asmundur;
    • Zink, Florian;
    • Lund, Sigrun H.;
    • Nawaz, Muhammad S.;
    • Bragi Walters, G.;
    • Skuladottir, Astros Th.;
    • Gudjonsson, Sigurjon A.;
    • Einarsson, Gudmundur;
    • Halldorsson, Gisli H.;
    • Bjarnadottir, Valgerdur;
    • Sveinbjornsson, Gardar;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Gudmundsson, Larus J.
    Publication type:
    Article

  • A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29133-7
    By:
    • Skuladottir, Astros Th.;
    • Bjornsdottir, Gyda;
    • Ferkingstad, Egil;
    • Einarsson, Gudmundur;
    • Stefansdottir, Lilja;
    • Nawaz, Muhammad Sulaman;
    • Oddsson, Asmundur;
    • Olafsdottir, Thorunn A.;
    • Saevarsdottir, Saedis;
    • Walters, G. Bragi;
    • Magnusson, Sigurdur H.;
    • Bjornsdottir, Anna;
    • Sveinsson, Olafur A.;
    • Vikingsson, Arnor;
    • Hansen, Thomas Folkmann;
    • Jacobsen, Rikke Louise;
    • Erikstrup, Christian;
    • Schwinn, Michael;
    • Brunak, Søren;
    • Banasik, Karina
    Publication type:
    Article

  • Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.

    Published in:
    2022
    By:
    • Bjornsdottir, Gyda;
    • Stefansdottir, Lilja;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Norland, Kristjan;
    • Ferkingstad, Egil;
    • Oddsson, Asmundur;
    • Zink, Florian;
    • Lund, Sigrun H.;
    • Nawaz, Muhammad S.;
    • Bragi Walters, G.;
    • Skuladottir, Astros Th.;
    • Gudjonsson, Sigurjon A.;
    • Einarsson, Gudmundur;
    • Halldorsson, Gisli H.;
    • Bjarnadottir, Valgerdur;
    • Sveinbjornsson, Gardar;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Gudmundsson, Larus J.
    Publication type:
    Correction Notice

  • A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29133-7
    By:
    • Skuladottir, Astros Th.;
    • Bjornsdottir, Gyda;
    • Ferkingstad, Egil;
    • Einarsson, Gudmundur;
    • Stefansdottir, Lilja;
    • Nawaz, Muhammad Sulaman;
    • Oddsson, Asmundur;
    • Olafsdottir, Thorunn A.;
    • Saevarsdottir, Saedis;
    • Walters, G. Bragi;
    • Magnusson, Sigurdur H.;
    • Bjornsdottir, Anna;
    • Sveinsson, Olafur A.;
    • Vikingsson, Arnor;
    • Hansen, Thomas Folkmann;
    • Jacobsen, Rikke Louise;
    • Erikstrup, Christian;
    • Schwinn, Michael;
    • Brunak, Søren;
    • Banasik, Karina
    Publication type:
    Article

  • Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
    By:
    • Bjornsdottir, Gyda;
    • Stefansdottir, Lilja;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Norland, Kristjan;
    • Ferkingstad, Egil;
    • Oddsson, Asmundur;
    • Zink, Florian;
    • Lund, Sigrun H.;
    • Nawaz, Muhammad S.;
    • Bragi Walters, G.;
    • Skuladottir, Astros Th.;
    • Gudjonsson, Sigurjon A.;
    • Einarsson, Gudmundur;
    • Halldorsson, Gisli H.;
    • Bjarnadottir, Valgerdur;
    • Sveinbjornsson, Gardar;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Gudmundsson, Larus J.
    Publication type:
    Article

  • Thirty novel sequence variants impacting human intracranial volume.

    Published in:
    Brain Communications, 2022, v. 4, n. 6, p. 1, doi. 10.1093/braincomms/fcac271
    By:
    • Nawaz, Muhammad Sulaman;
    • Einarsson, Gudmundur;
    • Bustamante, Mariana;
    • Gisladottir, Rosa S.;
    • Walters, G. Bragi;
    • Jonsdottir, Gudrun A.;
    • Skuladottir, Astros Th.;
    • Bjornsdottir, Gyda;
    • Magnusson, Sigurdur H.;
    • Asbjornsdottir, Bergrun;
    • Unnsteinsdottir, Unnur;
    • Sigurdsson, Engilbert;
    • Jonsson, Palmi V.;
    • Palmadottir, Vala Kolbrun;
    • Gudjonsson, Sigurjon A.;
    • Halldorsson, Gisli H.;
    • Ferkingstad, Egil;
    • Jonsdottir, Ingileif;
    • Thorleifsson, Gudmar;
    • Holm, Hilma
    Publication type:
    Article

  • A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02673-2
    By:
    • Skuladottir, Astros Th.;
    • Bjornsdottir, Gyda;
    • Nawaz, Muhammad Sulaman;
    • Petersen, Hannes;
    • Rognvaldsson, Solvi;
    • Moore, Kristjan Helgi Swerford;
    • Olafsson, Pall I.;
    • Magnusson, Sigurður H.;
    • Bjornsdottir, Anna;
    • Sveinsson, Olafur A.;
    • Sigurdardottir, Gudrun R.;
    • Saevarsdottir, Saedis;
    • Ivarsdottir, Erna V.;
    • Stefansdottir, Lilja;
    • Gunnarsson, Bjarni;
    • Muhlestein, Joseph B.;
    • Knowlton, Kirk U.;
    • Jones, David A.;
    • Nadauld, Lincoln D.;
    • Hartmann, Annette M.
    Publication type:
    Article

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

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-82736-w
    By:
    • Skuladottir, Astros Th.;
    • Bjornsdottir, Gyda;
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Nawaz, Muhammad Sulaman;
    • Moore, Kristjan Helgi Swerford;
    • Olason, Pall I.;
    • Thorgeirsson, Thorgeir E.;
    • Sigurpalsdottir, Brynja;
    • Sveinbjornsson, Gardar;
    • Eggertsson, Hannes P.;
    • Magnusson, Sigurdur H.;
    • Oddsson, Asmundur;
    • Bjornsdottir, Anna;
    • Vikingsson, Arnor;
    • Sveinsson, Olafur A.;
    • Hrafnsdottir, Maria G.;
    • Sigurdardottir, Gudrun R.;
    • Halldorsson, Bjarni V.;
    • Hansen, Thomas Folkmann
    Publication type:
    Article

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

    Published in:
    NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00752-9
    By:
    • Skuladottir, Astros Th.;
    • Tragante, Vinicius;
    • Sveinbjornsson, Gardar;
    • Helgason, Hannes;
    • Sturluson, Arni;
    • Bjornsdottir, Anna;
    • Jonsson, Palmi;
    • Palmadottir, Vala;
    • Sveinsson, Olafur A.;
    • Jensson, Brynjar O.;
    • Gudjonsson, Sigurjon A.;
    • Ivarsdottir, Erna V.;
    • Gisladottir, Rosa S.;
    • Gunnarsson, Arni F.;
    • Walters, G. Bragi;
    • Jonsdottir, Gudrun A.;
    • Thorgeirsson, Thorgeir E.;
    • Bjornsdottir, Gyda;
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.
    Publication type:
    Article