Found: 12

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  • Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.

    Published in:
    Nature Communications, 2016, v. 7, n. 2, p. 10572, doi. 10.1038/ncomms10572
    By:
    • Kristjansson, Ragnar P.;
    • Oddsson, Asmundur;
    • Helgason, Hannes;
    • Sveinbjornsson, Gardar;
    • Arnadottir, Gudny A.;
    • Jensson, Brynjar O.;
    • Jonasdottir, Aslaug;
    • Jonasdottir, Adalbjorg;
    • Bragi Walters, G.;
    • Sulem, Gerald;
    • Oskarsdottir, Arna;
    • Benonisdottir, Stefania;
    • Davidsson, Olafur B.;
    • Masson, Gisli;
    • Th Magnusson, Olafur;
    • Holm, Hilma;
    • Sigurdardottir, Olof;
    • Jonsdottir, Ingileif;
    • Eyjolfsson, Gudmundur I.;
    • Olafsson, Isleifur
    Publication type:
    Article

  • Common and rare variants associated with kidney stones and biochemical traits.

    Published in:
    Nature Communications, 2015, v. 6, n. 8, p. 7975, doi. 10.1038/ncomms8975
    By:
    • Oddsson, Asmundur;
    • Sulem, Patrick;
    • Helgason, Hannes;
    • Edvardsson, Vidar O.;
    • Thorleifsson, Gudmar;
    • Sveinbjörnsson, Gardar;
    • Haraldsdottir, Eik;
    • Eyjolfsson, Gudmundur I.;
    • Sigurdardottir, Olof;
    • Olafsson, Isleifur;
    • Masson, Gisli;
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.;
    • Thorsteinsdottir, Unnur;
    • Indridason, Olafur S.;
    • Palsson, Runolfur;
    • Stefansson, Kari
    Publication type:
    Article

  • A rare missense variant in NR1H4 associates with lower cholesterol levels.

    Published in:
    Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0015-9
    By:
    • Deaton, Aimee M.;
    • Sulem, Patrick;
    • Nioi, Paul;
    • Benonisdottir, Stefania;
    • Ward, Lucas D.;
    • Davidsson, Olafur B.;
    • Lao, Socheata;
    • Helgadottir, Anna;
    • Fan, Fan;
    • Jensson, Brynjar O.;
    • Norddahl, Gudmundur L.;
    • Jonasdottir, Aslaug;
    • Jonasdottir, Adalbjorg;
    • Sigurdsson, Asgeir;
    • Kristjansson, Ragnar P.;
    • Oddsson, Asmundur;
    • Arnadottir, Gudny A.;
    • Jonsson, Hakon;
    • Olafsson, Isleifur;
    • Eyjolfsson, Gudmundur I.
    Publication type:
    Article

  • Large-scale whole-genome sequencing of the Icelandic population.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 435, doi. 10.1038/ng.3247
    By:
    • Gudbjartsson, Daniel F;
    • Helgason, Hannes;
    • Gudbjartsson, Hakon;
    • Kong, Augustine;
    • Bjornsson, Einar S;
    • Olafsson, Sigurdur;
    • Thorarinsdottir, Hildur;
    • Theodors, Asgeir;
    • Steingrimsdottir, Thora;
    • Gudmundsdottir, Thora S;
    • Jonasson, Jon G;
    • Jonsson, Jon J;
    • Thorarensen, Olafur;
    • Ludvigsson, Petur;
    • Eyjolfsson, Gudmundur I;
    • Sigurdardottir, Olof;
    • Olafsson, Isleifur;
    • Gudjonsson, Sigurjon A;
    • Zink, Florian;
    • Oddson, Asmundur
    Publication type:
    Article

  • Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones-Role of Age and Comorbid Diseases.

    Published in:
    PLoS Genetics, 2010, v. 6, n. 7, p. 1, doi. 10.1371/journal.pgen.1001039
    By:
    • Gudbjartsson, Daniel F.;
    • Holm, Hilma;
    • Indridason, Olafur S.;
    • Thorleifsson, Gudmar;
    • Edvardsson, Vidar;
    • Sulem, Patrick;
    • de Vegt, Femmie;
    • d'Ancona, Frank C. H.;
    • den Heijer, Martin;
    • Franzson, Leifur;
    • Rafnar, Thorunn;
    • Kristjansson, Kristleifur;
    • Bjornsdottir, Unnur S.;
    • Eyjolfsson, Gudmundur I.;
    • Kiemeney, Lambertus A.;
    • Kong, Augustine;
    • Palsson, Runolfur;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article

  • Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06920-9
    By:
    • Gudmundsson, Julius;
    • Sigurdsson, Jon K.;
    • Stefansdottir, Lilja;
    • Agnarsson, Bjarni A.;
    • Isaksson, Helgi J.;
    • Stefansson, Olafur A.;
    • Gudjonsson, Sigurjon A.;
    • Gudbjartsson, Daniel F.;
    • Masson, Gisli;
    • Frigge, Michael L.;
    • Stacey, Simon N.;
    • Sulem, Patrick;
    • Halldorsson, Gisli H.;
    • Tragante, Vinicius;
    • Holm, Hilma;
    • Eyjolfsson, Gudmundur I.;
    • Sigurdardottir, Olof;
    • Olafsson, Isleifur;
    • Jonsson, Thorvaldur;
    • Jonsson, Eirikur
    Publication type:
    Article

  • Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels.

    Published in:
    Science Translational Medicine, 2010, v. 2, n. 62, p. 1, doi. 10.1126/scitranslmed.3001513
    By:
    • Gudmundsson, Julius;
    • Besenbacher, Soren;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Olafsson, Isleifur;
    • Arinbjarnarson, Sturla;
    • Agnarsson, Bjarni A.;
    • Benediktsdottir, Kristrun R.;
    • Isaksson, Helgi J.;
    • Kostic, Jelena P.;
    • Gudjonsson, Sigurjon A.;
    • Stacey, Simon N.;
    • Gylfason, Arnaldur;
    • Sigurdsson, Asgeir;
    • Holm, Hilma;
    • Bjornsdottir, Unnur S.;
    • Eyjolfsson, Gudmundur I.;
    • Navarrete, Sebastian;
    • Fuertes, Fernando;
    • Garcia-Prats, Maria D.
    Publication type:
    Article

  • Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14144-8
    By:
    • Olafsdottir, Thorunn A.;
    • Theodors, Fannar;
    • Bjarnadottir, Kristbjorg;
    • Bjornsdottir, Unnur Steina;
    • Agustsdottir, Arna B.;
    • Stefansson, Olafur A.;
    • Ivarsdottir, Erna V.;
    • Sigurdsson, Jon K.;
    • Benonisdottir, Stefania;
    • Eyjolfsson, Gudmundur I.;
    • Gislason, David;
    • Gislason, Thorarinn;
    • Guðmundsdóttir, Steinunn;
    • Gylfason, Arnaldur;
    • Halldorsson, Bjarni V.;
    • Halldorsson, Gisli H.;
    • Juliusdottir, Thorhildur;
    • Kristinsdottir, Anna M.;
    • Ludviksdottir, Dora;
    • Ludviksson, Bjorn R.
    Publication type:
    Article

  • Sequence variants associating with urinary biomarkers.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 7, p. 1199, doi. 10.1093/hmg/ddy409
    By:
    • Benonisdottir, Stefania;
    • Kristjansson, Ragnar P;
    • Oddsson, Asmundur;
    • Steinthorsdottir, Valgerdur;
    • Mikaelsdottir, Evgenia;
    • Kehr, Birte;
    • Jensson, Brynjar O;
    • Arnadottir, Gudny A;
    • Sulem, Gerald;
    • Sveinbjornsson, Gardar;
    • Kristmundsdottir, Snaedis;
    • Ivarsdottir, Erna V;
    • Tragante, Vinicius;
    • Gunnarsson, Bjarni;
    • Runolfsdottir, Hrafnhildur Linnet;
    • Arthur, Joseph G;
    • Deaton, Aimee M;
    • Eyjolfsson, Gudmundur I;
    • Davidsson, Olafur B;
    • Asselbergs, Folkert W
    Publication type:
    Article

  • A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 12, p. 2364, doi. 10.1093/hmg/ddx123
    By:
    • Bjornsson, Eythor;
    • Helgason, Hannes;
    • Halldorsson, Gisli;
    • Helgadottir, Anna;
    • Gylfason, Arnaldur;
    • Kehr, Birte;
    • Jonasdottir, Adalbjorg;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Oddsson, Asmundur;
    • Thorleifsson, Gudmar;
    • Magnusson, Olafur Th.;
    • Gretarsdottir, Solveig;
    • Zink, Florian;
    • Kristjansson, Ragnar P.;
    • Asgeirsdottir, Margret;
    • Swinkels, Dorine W.;
    • Kiemeney, Lambertus A.;
    • Eyjolfsson, Gudmundur I.;
    • Sigurdardottir, Olof
    Publication type:
    Article

  • Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.

    Published in:
    European Heart Journal, 2018, v. 39, n. 23, p. 2172, doi. 10.1093/eurheartj/ehy169
    By:
    • Helgadottir, Anna;
    • Sulem, Patrick;
    • Thorgeirsson, Gudmundur;
    • Gretarsdottir, Solveig;
    • Thorleifsson, Gudmar;
    • Jensson, Brynjar Ö;
    • Arnadottir, Gudny A;
    • Olafsson, Isleifur;
    • Eyjolfsson, Gudmundur I;
    • Sigurdardottir, Olof
    Publication type:
    Article

  • A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.

    Published in:
    PLoS Genetics, 2017, v. 13, n. 3, p. 1, doi. 10.1371/journal.pgen.1006659
    By:
    • Smith, Dirk;
    • Helgason, Hannes;
    • Sulem, Patrick;
    • Bjornsdottir, Unnur Steina;
    • Lim, Ai Ching;
    • Sveinbjornsson, Gardar;
    • Hasegawa, Haruki;
    • Brown, Michael;
    • Ketchem, Randal R.;
    • Gavala, Monica;
    • Garrett, Logan;
    • Jonasdottir, Adalbjorg;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Magnusson, Olafur T.;
    • Eyjolfsson, Gudmundur I.;
    • Olafsson, Isleifur;
    • Onundarson, Pall Torfi;
    • Sigurdardottir, Olof;
    • Gislason, David
    Publication type:
    Article