Found: 36

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  • Genetic insights into resting heart rate and its role in cardiovascular disease.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39521-2
    By:
    • van de Vegte, Yordi J.;
    • Eppinga, Ruben N.;
    • van der Ende, M. Yldau;
    • Hagemeijer, Yanick P.;
    • Mahendran, Yuvaraj;
    • Salfati, Elias;
    • Smith, Albert V.;
    • Tan, Vanessa Y.;
    • Arking, Dan E.;
    • Ntalla, Ioanna;
    • Appel, Emil V.;
    • Schurmann, Claudia;
    • Brody, Jennifer A.;
    • Rueedi, Rico;
    • Polasek, Ozren;
    • Sveinbjornsson, Gardar;
    • Lecoeur, Cecile;
    • Ladenvall, Claes;
    • Zhao, Jing Hua;
    • Isaacs, Aaron
    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

  • Rare mutations associating with serum creatinine and chronic kidney disease.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 25, p. 6935, doi. 10.1093/hmg/ddu399
    By:
    • Sveinbjornsson, Gardar;
    • Mikaelsdottir, Evgenia;
    • Palsson, Runolfur;
    • Indridason, Olafur S.;
    • Holm, Hilma;
    • Jonasdottir, Aslaug;
    • Helgason, Agnar;
    • Sigurdsson, Snaevar;
    • Jonasdottir, Adalbjorg;
    • Sigurdsson, Asgeir;
    • Eyjolfsson, Gudmundur Ingi;
    • Sigurdardottir, Olof;
    • Magnusson, Olafur Th.;
    • Kong, Augustine;
    • Masson, Gisli;
    • Sulem, Patrick;
    • Olafsson, Isleifur;
    • Thorsteinsdottir, Unnur;
    • Gudbjartsson, Daniel F.;
    • Stefansson, Kari
    Publication type:
    Article

  • Rare mutations associating with serum creatinine and chronic kidney disease.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu399
    By:
    • Sveinbjornsson, Gardar;
    • Mikaelsdottir, Evgenia;
    • Palsson, Runolfur;
    • Indridason, Olafur S.;
    • Holm, Hilma;
    • Jonasdottir, Aslaug;
    • Helgason, Agnar;
    • Sigurdsson, Snaevar;
    • Jonasdottir, Adalbjorg;
    • Sigurdsson, Asgeir;
    • Eyjolfsson, Gudmundur Ingi;
    • Sigurdardottir, Olof;
    • Magnusson, Olafur Th.;
    • Kong, Augustine;
    • Masson, Gisli;
    • Sulem, Patrick;
    • Olafsson, Isleifur;
    • Thorsteinsdottir, Unnur;
    • Gudbjartsson, Daniel F.;
    • Stefansson, Kari
    Publication type:
    Article

  • Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.

    Published in:
    Nature Communications, 2017, v. 8, n. 2, p. 14265, doi. 10.1038/ncomms14265
    By:
    • Bjornsdottir, Gyda;
    • Benonisdottir, Stefania;
    • Sveinbjornsson, Gardar;
    • Styrkarsdottir, Unnur;
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Bjornsson, Aron;
    • Olafsson, Ingvar H.;
    • Ulfarsson, Elfar;
    • Vikingsson, Arnor;
    • Hansdottir, Ragnheidur;
    • Karlsson, Karl O.;
    • Rafnar, Thorunn;
    • Jonsdottir, Ingileif;
    • Frigge, Michael L.;
    • Kong, Augustine;
    • Oddsson, Asmundur;
    • Masson, Gisli;
    • Magnusson, Olafur T.;
    • Gudbjartsson, Tomas
    Publication type:
    Article

  • Epigenetic and genetic components of height regulation.

    Published in:
    Nature Communications, 2016, v. 7, n. 11, p. 13490, doi. 10.1038/ncomms13490
    By:
    • Benonisdottir, Stefania;
    • Oddsson, Asmundur;
    • Helgason, Agnar;
    • Kristjansson, Ragnar P.;
    • Sveinbjornsson, Gardar;
    • Oskarsdottir, Arna;
    • Thorleifsson, Gudmar;
    • Davidsson, Olafur B.;
    • Arnadottir, Gudny A.;
    • Sulem, Gerald;
    • Jensson, Brynjar O.;
    • Holm, Hilma;
    • Alexandersson, Kristjan F.;
    • Tryggvadottir, Laufey;
    • Walters, G. Bragi;
    • Gudjonsson, Sigurjon A.;
    • Ward, Lucas D.;
    • Sigurdsson, Jon K.;
    • Iordache, Paul D.;
    • Frigge, Michael L.
    Publication type:
    Article

  • 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

  • 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:
    • Oskarsson, Gudjon R.;
    • Kristjansson, Ragnar P.;
    • Lee, Amy L.;
    • Sveinbjornsson, Gardar;
    • Magnusson, Magnus K.;
    • Ivarsdottir, Erna V.;
    • Benonisdottir, Stefania;
    • Oddsson, Asmundur;
    • Davidsson, Olafur B.;
    • Saemundsdottir, Jona;
    • Halldorsson, Gisli H.;
    • Arthur, Joseph;
    • Arnadottir, Gudny A.;
    • Masson, Gisli;
    • Jensson, Brynjar O.;
    • Holm, Hilma;
    • Olafsson, Isleifur;
    • Onundarson, Pall T.;
    • Gudbjartsson, Daniel F.;
    • Norddahl, Gudmundur L.
    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

  • 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

  • Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05428-6
    By:
    • Rafnar, Thorunn;
    • Gunnarsson, Bjarni;
    • Stefansson, Olafur A.;
    • Sulem, Patrick;
    • Ingason, Andres;
    • Frigge, Michael L.;
    • Stefansdottir, Lilja;
    • Sigurdsson, Jon K.;
    • Tragante, Vinicius;
    • Steinthorsdottir, Valgerdur;
    • Styrkarsdottir, Unnur;
    • Stacey, Simon N.;
    • Gudmundsson, Julius;
    • Arnadottir, Gudny A.;
    • Oddsson, Asmundur;
    • Zink, Florian;
    • Halldorsson, Gisli;
    • Sveinbjornsson, Gardar;
    • Kristjansson, Ragnar P.;
    • Davidsson, Olafur B.
    Publication type:
    Article

  • MAP1B mutations cause intellectual disability and extensive white matter deficit.

    Published in:
    Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-05595-6
    By:
    • Walters, G. Bragi;
    • Gustafsson, Omar;
    • Sveinbjornsson, Gardar;
    • Eiriksdottir, Valgerdur K.;
    • Agustsdottir, Arna B.;
    • Jonsdottir, Gudrun A.;
    • Steinberg, Stacy;
    • Gunnarsson, Arni F.;
    • Magnusson, Magnus I.;
    • Unnsteinsdottir, Unnur;
    • Lee, Amy L.;
    • Jonasdottir, Adalbjorg;
    • Sigurdsson, Asgeir;
    • Jonasdottir, Aslaug;
    • Skuladottir, Astros;
    • Jonsson, Lina;
    • Nawaz, Muhammad S.;
    • Sulem, Patrick;
    • Frigge, Mike;
    • Ingason, Andres
    Publication type:
    Article

  • Genetic variants associated with syncope implicate neural and autonomic processes.

    Published in:
    European Heart Journal, 2023, v. 44, n. 12, p. 1070, doi. 10.1093/eurheartj/ehad016
    By:
    • Aegisdottir, Hildur M;
    • Thorolfsdottir, Rosa B;
    • Sveinbjornsson, Gardar;
    • Stefansson, Olafur A;
    • Gunnarsson, Bjarni;
    • Tragante, Vinicius;
    • Thorleifsson, Gudmar;
    • Stefansdottir, Lilja;
    • Thorgeirsson, Thorgeir E;
    • Ferkingstad, Egil;
    • Sulem, Patrick;
    • Norddahl, Gudmundur;
    • Rutsdottir, Gudrun;
    • Banasik, Karina;
    • Christensen, Alex Hoerby;
    • Mikkelsen, Christina;
    • Pedersen, Ole Birger;
    • Brunak, Søren;
    • Bruun, Mie Topholm;
    • Erikstrup, Christian
    Publication type:
    Article

  • Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.

    Published in:
    Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1457-6
    By:
    • Prins, Bram P.;
    • Mead, Timothy J.;
    • Brody, Jennifer A.;
    • Sveinbjornsson, Gardar;
    • Ntalla, Ioanna;
    • Bihlmeyer, Nathan A.;
    • van den Berg, Marten;
    • Bork-Jensen, Jette;
    • Cappellani, Stefania;
    • Van Duijvenboden, Stefan;
    • Klena, Nikolai T.;
    • Gabriel, George C.;
    • Liu, Xiaoqin;
    • Gulec, Cagri;
    • Grarup, Niels;
    • Haessler, Jeffrey;
    • Hall, Leanne M.;
    • Iorio, Annamaria;
    • Isaacs, Aaron;
    • Li-Gao, Ruifang
    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

  • 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

  • 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

  • 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

  • Age and Influenza-Specific Pre-Vaccination Antibodies Strongly Affect Influenza Vaccine Responses in the Icelandic Population whereas Disease and Medication Have Small Effects.

    Published in:
    Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2017.01872
    By:
    • Olafsdottir, Thorunn A.;
    • Alexandersson, Kristjan F.;
    • Sveinbjornsson, Gardar;
    • Lapini, Giulia;
    • Palladino, Laura;
    • Montomoli, Emanuele;
    • Del Giudice, Giuseppe;
    • Gudbjartsson, Daniel F.;
    • Jonsdottir, Ingileif
    Publication type:
    Article

  • Causal stability ranking.

    Published in:
    Bioinformatics, 2012, v. 28, n. 21, p. 2819, doi. 10.1093/bioinformatics/bts523
    By:
    • Stekhoven, Daniel J.;
    • Moraes, Izabel;
    • Sveinbjörnsson, Gardar;
    • Hennig, Lars;
    • Maathuis, Marloes H.;
    • Bühlmann, Peter
    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

  • Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15706-x
    By:
    • Ntalla, Ioanna;
    • Weng, Lu-Chen;
    • Cartwright, James H.;
    • Hall, Amelia Weber;
    • Sveinbjornsson, Gardar;
    • Tucker, Nathan R.;
    • Choi, Seung Hoan;
    • Chaffin, Mark D.;
    • Roselli, Carolina;
    • Barnes, Michael R.;
    • Mifsud, Borbala;
    • Warren, Helen R.;
    • Hayward, Caroline;
    • Marten, Jonathan;
    • Cranley, James J.;
    • Concas, Maria Pina;
    • Gasparini, Paolo;
    • Boutin, Thibaud;
    • Kolcic, Ivana;
    • Polasek, Ozren
    Publication type:
    Article

  • Sequence variants with large effects on cardiac electrophysiology and disease.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12682-9
    By:
    • Norland, Kristjan;
    • Sveinbjornsson, Gardar;
    • Thorolfsdottir, Rosa B.;
    • Davidsson, Olafur B.;
    • Tragante, Vinicius;
    • Rajamani, Sridharan;
    • Helgadottir, Anna;
    • Gretarsdottir, Solveig;
    • van Setten, Jessica;
    • Asselbergs, Folkert W.;
    • Sverrisson, Jon Th.;
    • Stephensen, Sigurdur S.;
    • Oskarsson, Gylfi;
    • Sigurdsson, Emil L.;
    • Andersen, Karl;
    • Danielsen, Ragnar;
    • Thorgeirsson, Gudmundur;
    • Thorsteinsdottir, Unnur;
    • Arnar, David O.;
    • Sulem, Patrick
    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

  • Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.

    Published in:
    Journal of the American Heart Association, 2023, v. 12, n. 14, p. 1, doi. 10.1161/JAHA.123.029845
    By:
    • Sveinbjornsson, Gardar;
    • Benediktsdottir, Bara D.;
    • Sigfusson, Gunnlaugur;
    • Norland, Kristjan;
    • Davidsson, Olafur B.;
    • Thorolfsdottir, Rosa B.;
    • Tragante, Vinicius;
    • Arnadottir, Gudny A.;
    • Jensson, Brynjar O.;
    • Katrinardottir, Hildigunnur;
    • Fridriksdottir, Run;
    • Gudmundsdottir, Hallbera;
    • Aegisdottir, Hildur M.;
    • Fridriksson, Brynjar;
    • Thorgeirsson, Gudmundur;
    • Magnusson, Vidar;
    • Oddsson, Asmundur;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Holm, Hilma
    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

  • 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

  • Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.

    Published in:
    European Heart Journal, 2020, v. 41, n. 28, p. 2618, doi. 10.1093/eurheartj/ehaa531
    By:
    • Helgadottir, Anna;
    • Thorleifsson, Gudmar;
    • Alexandersson, Kristjan F;
    • Tragante, Vinicius;
    • Thorsteinsdottir, Margret;
    • Eiriksson, Finnur F;
    • Gretarsdottir, Solveig;
    • Björnsson, Eythór;
    • Magnusson, Olafur;
    • Sveinbjornsson, Gardar;
    • Jonsdottir, Ingileif;
    • Steinthorsdottir, Valgerdur;
    • Ferkingstad, Egil;
    • Jensson, Brynjar Ö;
    • Stefansson, Hreinn;
    • Olafsson, Isleifur;
    • Christensen, Alex H;
    • Torp-Pedersen, Christian;
    • Køber, Lars;
    • Pedersen, Ole B
    Publication type:
    Article

  • A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.

    Published in:
    European Heart Journal, 2018, v. 39, n. 34, p. 3243, doi. 10.1093/eurheartj/ehy142
    By:
    • Bjornsson, Thorsteinn;
    • Thorolfsdottir, Rosa B;
    • Sveinbjornsson, Gardar;
    • Sulem, Patrick;
    • Norddahl, Gudmundur L;
    • Helgadottir, Anna;
    • Gretarsdottir, Solveig;
    • Magnusdottir, Audur;
    • Danielsen, Ragnar;
    • Sigurdsson, Emil L
    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

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

    Published in:
    Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-05079-4
    By:
    • Kristjansson, Ragnar P.;
    • Oskarsson, Gudjon R.;
    • Skuladottir, Astros;
    • Oddsson, Asmundur;
    • Rognvaldsson, Solvi;
    • Sveinbjornsson, Gardar;
    • Lund, Sigrun H.;
    • Jensson, Brynjar O.;
    • Styrmisdottir, Edda L.;
    • Halldorsson, Gisli H.;
    • Ferkingstad, Egil;
    • Eldjarn, Grimur Hjorleifsson;
    • Beyter, Doruk;
    • Kristmundsdottir, Snædis;
    • Juliusson, Kristinn;
    • Fridriksdottir, Run;
    • Arnadottir, Gudny A.;
    • Katrinardottir, Hildigunnur;
    • Snorradottir, Margret H.;
    • Tragante, Vinicius
    Publication type:
    Article