Found: 5

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  • A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.

    Published in:
    European Heart Journal, 2017, v. 38, n. 1, p. 1, doi. 10.1093/eurheartj/ehw379
    By:
    • Gudbjartsson, Daniel F.;
    • Holm, Hilma;
    • Sulem, Patrick;
    • Masson, Gisli;
    • Oddsson, Asmundur;
    • Magnusson, Olafur Th.;
    • Saemundsdottir, Jona;
    • Helgadottir, Hafdis Th.;
    • Helgason, Hannes;
    • Johannsdottir, Hrefna;
    • Gretarsdottir, Solveig;
    • Gudjonsson, Sigurjon A.;
    • Njølstad, Inger;
    • Løchen, Maja-Lisa;
    • Baum, Larry;
    • Ma, Ronald C.W.;
    • Sigfusson, Gunnlaugur;
    • Kong, Augustine;
    • Thorgeirsson, Guðmundur;
    • Sverrisson, Jon Th.
    Publication type:
    Article

  • A common variant at 8q24.21 is associated with renal cell cancer.

    Published in:
    Nature Communications, 2013, v. 4, n. 11, p. 2776, doi. 10.1038/ncomms3776
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Masson, Gisli;
    • Petursdottir, Vigdis;
    • Hardarson, Sverrir;
    • Gudjonsson, Sigurjon A.;
    • Johannsdottir, Hrefna;
    • Helgadottir, Hafdis Th.;
    • Stacey, Simon N.;
    • Magnusson, Olafur Th.;
    • Helgason, Hannes;
    • Panadero, Angeles;
    • van der Zanden, Loes F.;
    • Aben, Katja K. H.;
    • Vermeulen, Sita H.;
    • Oosterwijk, Egbert;
    • Kong, Augustine;
    • Mayordomo, Jose I.;
    • Sverrisdottir, Asgerdur
    Publication type:
    Article

  • A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 12, p. 1326, doi. 10.1038/ng.2437
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F;
    • Masson, Gisli;
    • Agnarsson, Bjarni A;
    • Benediktsdottir, Kristrun R;
    • Sigurdsson, Asgeir;
    • Magnusson, Olafur Th;
    • Gudjonsson, Sigurjon A;
    • Magnusdottir, Droplaug N;
    • Johannsdottir, Hrefna;
    • Helgadottir, Hafdis Th;
    • Stacey, Simon N;
    • Jonasdottir, Adalbjorg;
    • Olafsdottir, Stefania B;
    • Thorleifsson, Gudmar;
    • Jonasson, Jon G;
    • Tryggvadottir, Laufey;
    • Navarrete, Sebastian;
    • Fuertes, Fernando
    Publication type:
    Article

  • Discovery of common variants associated with low TSH levels and thyroid cancer risk.

    Published in:
    Nature Genetics, 2012, v. 44, n. 3, p. 319, doi. 10.1038/ng.1046
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F;
    • Jonasson, Jon G;
    • Masson, Gisli;
    • He, Huiling;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Stacey, Simon N;
    • Johannsdottir, Hrefna;
    • Th Helgadottir, Hafdis;
    • Li, Wei;
    • Nagy, Rebecca;
    • Ringel, Matthew D;
    • Kloos, Richard T;
    • de Visser, Marieke C H;
    • Plantinga, Theo S;
    • den Heijer, Martin;
    • Aguillo, Esperanza;
    • Panadero, Angeles
    Publication type:
    Article

  • A rare variant in MYH6 is associated with high risk of sick sinus syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 316, doi. 10.1038/ng.781
    By:
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.;
    • Sulem, Patrick;
    • Masson, Gisli;
    • Helgadottir, Hafdis Th;
    • Zanon, Carlo;
    • Magnusson, Olafur Th;
    • Helgason, Agnar;
    • Saemundsdottir, Jona;
    • Gylfason, Arnaldur;
    • Stefansdottir, Hrafnhildur;
    • Gretarsdottir, Solveig;
    • Matthiasson, Stefan E.;
    • Thorgeirsson, Guðmundur;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Stefansson, Hreinn;
    • Werge, Thomas;
    • Rafnar, Thorunn;
    • Kiemeney, Lambertus A.
    Publication type:
    Article