Found: 31

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  • Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

    Published in:
    2022
    By:
    • Ajore, Ram;
    • Niroula, Abhishek;
    • Pertesi, Maroulio;
    • Cafaro, Caterina;
    • Thodberg, Malte;
    • Went, Molly;
    • Bao, Erik L.;
    • Duran-Lozano, Laura;
    • Lopez de Lapuente Portilla, Aitzkoa;
    • Olafsdottir, Thorunn;
    • Ugidos-Damboriena, Nerea;
    • Magnusson, Olafur;
    • Samur, Mehmet;
    • Lareau, Caleb A.;
    • Halldorsson, Gisli H.;
    • Thorleifsson, Gudmar;
    • Norddahl, Gudmundur L.;
    • Gunnarsdottir, Kristbjorg;
    • Försti, Asta;
    • Goldschmidt, Hartmut
    Publication type:
    Correction Notice
  • 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
  • Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33076-4
    By:
    • Norddahl, Gudmundur L.;
    • Melsted, Pall;
    • Gunnarsdottir, Kristbjorg;
    • Halldorsson, Gisli H.;
    • Olafsdottir, Thorunn A.;
    • Gylfason, Arnaldur;
    • Kristjansson, Mar;
    • Magnusson, Olafur T.;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Thorsteinsdottir, Unnur;
    • Jonsdottir, Ingileif;
    • Stefansson, Kari
    Publication type:
    Article
  • Genetic architecture of band neutrophil fraction in Iceland.

    Published in:
    Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03462-1
    By:
    • Oskarsson, Gudjon R.;
    • Magnusson, Magnus K.;
    • Oddsson, Asmundur;
    • Jensson, Brynjar O.;
    • Fridriksdottir, Run;
    • Arnadottir, Gudny A.;
    • Katrinardottir, Hildigunnur;
    • Rognvaldsson, Solvi;
    • Halldorsson, Gisli H.;
    • Sveinbjornsson, Gardar;
    • Ivarsdottir, Erna V.;
    • Stefansdottir, Lilja;
    • Ferkingstad, Egil;
    • Norland, Kristjan;
    • Tragante, Vinicius;
    • Saemundsdottir, Jona;
    • Jonasdottir, Aslaug;
    • Jonasdottir, Adalbjorg;
    • Sigurjonsdottir, Svanhvit;
    • Petursdottir, Karen O.
    Publication type:
    Article
  • The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02224-9
    By:
    • Ivarsdottir, Erna V.;
    • Holm, Hilma;
    • Benonisdottir, Stefania;
    • Olafsdottir, Thorhildur;
    • Sveinbjornsson, Gardar;
    • Thorleifsson, Gudmar;
    • Eggertsson, Hannes P.;
    • Halldorsson, Gisli H.;
    • Hjorleifsson, Kristjan E.;
    • Melsted, Pall;
    • Gylfason, Arnaldur;
    • Arnadottir, Gudny A.;
    • Oddsson, Asmundur;
    • Jensson, Brynjar O.;
    • Jonasdottir, Aslaug;
    • Jonasdottir, Adalbjorg;
    • Juliusdottir, Thorhildur;
    • Stefansdottir, Lilja;
    • Tragante, Vinicius;
    • Halldorsson, Bjarni V.
    Publication type:
    Article
  • Comparing migraine with and without aura to healthy controls using RNA sequencing.

    Published in:
    2019
    By:
    • Kogelman, Lisette JA;
    • Falkenberg, Katrine;
    • Halldorsson, Gisli H;
    • Poulsen, Lau U;
    • Worm, Jacob;
    • Ingason, Andres;
    • Stefansson, Hreinn;
    • Stefansson, Kari;
    • Hansen, Thomas F;
    • Olesen, Jes
    Publication type:
    journal 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
  • 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
  • Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27666-x
    By:
    • Ajore, Ram;
    • Niroula, Abhishek;
    • Pertesi, Maroulio;
    • Cafaro, Caterina;
    • Thodberg, Malte;
    • Went, Molly;
    • Bao, Erik L.;
    • Duran-Lozano, Laura;
    • Lopez de Lapuente Portilla, Aitzkoa;
    • Olafsdottir, Thorunn;
    • Ugidos-Damboriena, Nerea;
    • Magnusson, Olafur;
    • Samur, Mehmet;
    • Lareau, Caleb A.;
    • Halldorsson, Gisli H.;
    • Thorleifsson, Gudmar;
    • Norddahl, Gudmundur L.;
    • Gunnarsdottir, Kristbjorg;
    • Försti, Asta;
    • Goldschmidt, Hartmut
    Publication type:
    Article
  • Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

    Published in:
    2023
    By:
    • Oddsson, Asmundur;
    • Sulem, Patrick;
    • Sveinbjornsson, Gardar;
    • Arnadottir, Gudny A.;
    • Steinthorsdottir, Valgerdur;
    • Halldorsson, Gisli H.;
    • Atlason, Bjarni A.;
    • Oskarsson, Gudjon R.;
    • Helgason, Hannes;
    • Nielsen, Henriette Svarre;
    • Westergaard, David;
    • Karjalainen, Juha M.;
    • Katrinardottir, Hildigunnur;
    • Fridriksdottir, Run;
    • Jensson, Brynjar O.;
    • Tragante, Vinicius;
    • Ferkingstad, Egil;
    • Jonsson, Hakon;
    • Gudjonsson, Sigurjon A.;
    • Beyter, Doruk
    Publication type:
    Correction Notice
  • Sequence variants affecting the genome-wide rate of germline microsatellite mutations.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39547-6
    By:
    • Kristmundsdottir, Snaedis;
    • Jonsson, Hakon;
    • Hardarson, Marteinn T.;
    • Palsson, Gunnar;
    • Beyter, Doruk;
    • Eggertsson, Hannes P.;
    • Gylfason, Arnaldur;
    • Sveinbjornsson, Gardar;
    • Holley, Guillaume;
    • Stefansson, Olafur A.;
    • Halldorsson, Gisli H.;
    • Olafsson, Sigurgeir;
    • Arnadottir, Gudny. A.;
    • Olason, Pall I.;
    • Eiriksson, Ogmundur;
    • Masson, Gisli;
    • Thorsteinsdottir, Unnur;
    • Rafnar, Thorunn;
    • Sulem, Patrick;
    • Helgason, Agnar
    Publication type:
    Article
  • Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38951-2
    By:
    • Oddsson, Asmundur;
    • Sulem, Patrick;
    • Sveinbjornsson, Gardar;
    • Arnadottir, Gudny A.;
    • Steinthorsdottir, Valgerdur;
    • Halldorsson, Gisli H.;
    • Atlason, Bjarni A.;
    • Oskarsson, Gudjon R.;
    • Helgason, Hannes;
    • Nielsen, Henriette Svarre;
    • Westergaard, David;
    • Karjalainen, Juha M.;
    • Katrinardottir, Hildigunnur;
    • Fridriksdottir, Run;
    • Jensson, Brynjar O.;
    • Tragante, Vinicius;
    • Ferkingstad, Egil;
    • Jonsson, Hakon;
    • Gudjonsson, Sigurjon A.;
    • Beyter, Doruk
    Publication type:
    Article
  • Genetic insight into sick sinus syndrome.

    Published in:
    European Heart Journal, 2021, v. 42, n. 20, p. 1959, doi. 10.1093/eurheartj/ehaa1108
    By:
    • Thorolfsdottir, Rosa B;
    • Sveinbjornsson, Gardar;
    • Aegisdottir, Hildur M;
    • Benonisdottir, Stefania;
    • Stefansdottir, Lilja;
    • Ivarsdottir, Erna V;
    • Halldorsson, Gisli H;
    • Sigurdsson, Jon K;
    • Torp-Pedersen, Christian;
    • Weeke, Peter E;
    • Brunak, Søren;
    • Westergaard, David;
    • Pedersen, Ole B;
    • Sorensen, Erik;
    • Nielsen, Kaspar R;
    • Burgdorf, Kristoffer S;
    • Banasik, Karina;
    • Brumpton, Ben;
    • Zhou, Wei;
    • Oddsson, Asmundur
    Publication type:
    Article
  • GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09860-0
    By:
    • Styrkarsdottir, Unnur;
    • Stefansson, Olafur A.;
    • Gunnarsdottir, Kristbjorg;
    • Thorleifsson, Gudmar;
    • Lund, Sigrun H.;
    • Stefansdottir, Lilja;
    • Juliusson, Kristinn;
    • Agustsdottir, Arna B.;
    • Zink, Florian;
    • Halldorsson, Gisli H.;
    • Ivarsdottir, Erna V.;
    • Benonisdottir, Stefania;
    • Jonsson, Hakon;
    • Gylfason, Arnaldur;
    • Norland, Kristjan;
    • Trajanoska, Katerina;
    • Boer, Cindy G.;
    • Southam, Lorraine;
    • Leung, Jason C. S.;
    • Tang, Nelson L. S.
    Publication type:
    Article
  • Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07460-y
    By:
    • Ferkingstad, Egil;
    • Oddsson, Asmundur;
    • Gretarsdottir, Solveig;
    • Benonisdottir, Stefania;
    • Thorleifsson, Gudmar;
    • Deaton, Aimee M.;
    • Jonsson, Stefan;
    • Stefansson, Olafur A.;
    • Norddahl, Gudmundur L.;
    • Zink, Florian;
    • Arnadottir, Gudny A.;
    • Gunnarsson, Bjarni;
    • Halldorsson, Gisli H.;
    • Helgadottir, Anna;
    • Jensson, Brynjar O.;
    • Kristjansson, Ragnar P.;
    • Sveinbjornsson, Gardar;
    • Sverrisson, David A.;
    • Masson, Gisli;
    • Olafsson, Isleifur
    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
  • A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-020-01575-z
    By:
    • Bell, Steven;
    • Rigas, Andreas S.;
    • Magnusson, Magnus K.;
    • Ferkingstad, Egil;
    • Allara, Elias;
    • Bjornsdottir, Gyda;
    • Ramond, Anna;
    • Sørensen, Erik;
    • Halldorsson, Gisli H.;
    • Paul, Dirk S.;
    • Burgdorf, Kristoffer S.;
    • Eggertsson, Hannes P.;
    • Howson, Joanna M. M.;
    • Thørner, Lise W.;
    • Kristmundsdottir, Snaedis;
    • Astle, William J.;
    • Erikstrup, Christian;
    • Sigurdsson, Jon K.;
    • Vuckovic, Dragana;
    • Dinh, Khoa M.
    Publication type:
    Article
  • Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.

    Published in:
    Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0921-5
    By:
    • Oskarsson, Gudjon R.;
    • Oddsson, Asmundur;
    • Magnusson, Magnus K.;
    • Kristjansson, Ragnar P.;
    • Halldorsson, Gisli H.;
    • Ferkingstad, Egil;
    • Zink, Florian;
    • Helgadottir, Anna;
    • Ivarsdottir, Erna V.;
    • Arnadottir, Gudny A.;
    • Jensson, Brynjar O.;
    • Katrinardottir, Hildigunnur;
    • Sveinbjornsson, Gardar;
    • Kristinsdottir, Anna M.;
    • Lee, Amy L.;
    • Saemundsdottir, Jona;
    • Stefansdottir, Lilja;
    • Sigurdsson, Jon K.;
    • Davidsson, Olafur B.;
    • Benonisdottir, Stefania
    Publication type:
    Article
  • Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.

    Published in:
    Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0857-9
    By:
    • Olafsdottir, Thorhildur;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Stefansson, Olafur A.;
    • Medek, Helga;
    • Olafsson, Karl;
    • Ingthorsson, Orri;
    • Gudmundsson, Valur;
    • Jonsdottir, Ingileif;
    • Halldorsson, Gisli H.;
    • Kristjansson, Ragnar P.;
    • Frigge, Michael L.;
    • Stefansdottir, Lilja;
    • Sigurdsson, Jon K.;
    • Oddsson, Asmundur;
    • Sigurdsson, Asgeir;
    • Eggertsson, Hannes P.;
    • Melsted, Pall;
    • Halldorsson, Bjarni V.;
    • Lund, Sigrun H.
    Publication type:
    Article
  • Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.

    Published in:
    Nature Communications, 2017, v. 8, n. 6, p. 15789, doi. 10.1038/ncomms15789
    By:
    • Sigurdsson, Snaevar;
    • Alexandersson, Kristjan F.;
    • Sulem, Patrick;
    • Feenstra, Bjarke;
    • Gudmundsdottir, Steinunn;
    • Halldorsson, Gisli H.;
    • Olafsson, Sigurgeir;
    • Sigurdsson, Asgeir;
    • Rafnar, Thorunn;
    • Thorgeirsson, Thorgeir;
    • Sørensen, Erik;
    • Nordholm-Carstensen, Andreas;
    • Burcharth, Jakob;
    • Andersen, Jens;
    • Jørgensen, Henrik Stig;
    • Possfelt-Møller, Emma;
    • Ullum, Henrik;
    • Thorleifsson, Gudmar;
    • Masson, Gisli;
    • Thorsteinsdottir, Unnur
    Publication type:
    Article
  • A genome-wide association study yields five novel thyroid cancer risk loci.

    Published in:
    Nature Communications, 2017, v. 8, n. 2, p. 14517, doi. 10.1038/ncomms14517
    By:
    • Gudmundsson, Julius;
    • Thorleifsson, Gudmar;
    • Sigurdsson, Jon K.;
    • Stefansdottir, Lilja;
    • Jonasson, Jon G.;
    • Gudjonsson, Sigurjon A.;
    • Gudbjartsson, Daniel F.;
    • Masson, Gisli;
    • Johannsdottir, Hrefna;
    • Halldorsson, Gisli H.;
    • Stacey, Simon N.;
    • Helgason, Hannes;
    • Sulem, Patrick;
    • Senter, Leigha;
    • He, Huiling;
    • Liyanarachchi, Sandya;
    • Ringel, Matthew D.;
    • Aguillo, Esperanza;
    • Panadero, Angeles;
    • Prats, Enrique
    Publication type:
    Article
  • Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.

    Published in:
    Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
    By:
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Aradottir, Kristrun;
    • Feenstra, Bjarke;
    • Sigurdsson, Asgeir;
    • Stefansdottir, Lilja;
    • Kristinsdottir, Anna M.;
    • Zink, Florian;
    • Halldorsson, Gisli H.;
    • Munk Nielsen, Nete;
    • Geller, Frank;
    • Melbye, Mads;
    • Gudbjartsson, Daniel F.;
    • Geirsson, Reynir T.;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    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
  • Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk.

    Published in:
    2021
    By:
    • Duran-Lozano, Laura;
    • Thorleifsson, Gudmar;
    • Lopez de Lapuente Portilla, Aitzkoa;
    • Niroula, Abhishek;
    • Went, Molly;
    • Thodberg, Malte;
    • Pertesi, Maroulio;
    • Ajore, Ram;
    • Cafaro, Caterina;
    • Olason, Pall I.;
    • Stefansdottir, Lilja;
    • Bragi Walters, G.;
    • Halldorsson, Gisli H.;
    • Turesson, Ingemar;
    • Kaiser, Martin F.;
    • Weinhold, Niels;
    • Abildgaard, Niels;
    • Andersen, Niels Frost;
    • Mellqvist, Ulf-Henrik;
    • Waage, Anders
    Publication type:
    Correction Notice
  • Germline variants at SOHLH2 influence multiple myeloma risk.

    Published in:
    Blood Cancer Journal, 2021, v. 11, n. 4, p. 1, doi. 10.1038/s41408-021-00468-6
    By:
    • Duran-Lozano, Laura;
    • Thorleifsson, Gudmar;
    • Lopez de Lapuente Portilla, Aitzkoa;
    • Niroula, Abhishek;
    • Went, Molly;
    • Thodberg, Malte;
    • Pertesi, Maroulio;
    • Ajore, Ram;
    • Cafaro, Caterina;
    • Olason, Pall I.;
    • Stefansdottir, Lilja;
    • Bragi Walters, G.;
    • Halldorsson, Gisli H.;
    • Turesson, Ingemar;
    • Kaiser, Martin F.;
    • Weinhold, Niels;
    • Abildgaard, Niels;
    • Andersen, Niels Frost;
    • Mellqvist, Ulf-Henrik;
    • Waage, Anders
    Publication type:
    Article
  • Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.

    Published in:
    Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0068-9
    By:
    • Thorolfsdottir, Rosa B.;
    • Sveinbjornsson, Gardar;
    • Sulem, Patrick;
    • Nielsen, Jonas B.;
    • Jonsson, Stefan;
    • Halldorsson, Gisli H.;
    • Melsted, Pall;
    • Ivarsdottir, Erna V.;
    • Davidsson, Olafur B.;
    • Kristjansson, Ragnar P.;
    • Thorleifsson, Gudmar;
    • Helgadottir, Anna;
    • Gretarsdottir, Solveig;
    • Norddahl, Gudmundur;
    • Rajamani, Sridharan;
    • Torfason, Bjarni;
    • Valgardsson, Atli S.;
    • Sverrisson, Jon T.;
    • Tragante, Vinicius;
    • Holmen, Oddgeir L.
    Publication type:
    Article
  • A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin.

    Published in:
    Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0053-3
    By:
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