Found: 34

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  • Effects of a 5-Lipoxygenase–Activating Protein Inhibitor on Biomarkers Associated With Risk of Myocardial Infarction: A Randomized Trial.

    Published in:
    JAMA: Journal of the American Medical Association, 2005, v. 293, n. 18, p. 2245, doi. 10.1001/jama.293.18.2245
    By:
    • Hakonarson, Hakon;
    • Thorvaldsson, Sverrir;
    • Helgadottir, Anna;
    • Gudbjartsson, Daniel;
    • Zink, Florian;
    • Andresdottir, Margret;
    • Manolescu, Andrei;
    • Arnar, David O.;
    • Andersen, Karl;
    • Sigurdsson, Axel;
    • Thorgeirsson, Gestur;
    • Jonsson, Asgeir;
    • Agnarsson, Uggi;
    • Bjornsdottir, Halldora;
    • Gottskalksson, Gizur;
    • Einarsson, Atli;
    • Gudmundsdottir, Hrefna;
    • Adalsteinsdottir, Asdis E.;
    • Gudmundsson, Kolbeinn;
    • Kristjansson, Kristleifur
    Publication type:
    Article

  • Time course analysis of gene expression identifies multiple genes with differential expression in patients with in-stent restenosis.

    Published in:
    BMC Medical Genomics, 2011, v. 4, n. 1, p. 20, doi. 10.1186/1755-8794-4-20
    By:
    • Ganesh, Santhi K.;
    • Jungnam Joo;
    • Skelding, Kimberly;
    • Mehta, Laxmi;
    • Gang Zheng;
    • O'Neill, Kathleen;
    • Billings, Eric M.;
    • Helgadottir, Anna;
    • Andersen, Karl;
    • Thorgeirsson, Gudmundur;
    • Gudnason, Thorarinn;
    • Geller, Nancy L.;
    • Simari, Robert D.;
    • Holmes, David R.;
    • O'Neill, William W.;
    • Nabel, Elizabeth G.
    Publication type:
    Article

  • A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2941, doi. 10.1093/hmg/ddt141
    By:
    • Jones, Gregory T.;
    • Bown, Matthew J.;
    • Gretarsdottir, Solveig;
    • Romaine, Simon P.R.;
    • Helgadottir, Anna;
    • Yu, Grace;
    • Tromp, Gerard;
    • Norman, Paul E.;
    • Jin, Cao;
    • Baas, Annette F.;
    • Blankensteijn, Jan D.;
    • Kullo, Iftikhar J.;
    • Phillips, L. Victoria;
    • Williams, Michael J.A.;
    • Topless, Ruth;
    • Merriman, Tony R.;
    • Vasudevan, Thodor M.;
    • Lewis, David R.;
    • Blair, Ross D.;
    • Hill, Andrew A.
    Publication type:
    Article

  • Genome-wide analysis yields new loci associating with aortic valve stenosis.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03252-6
    By:
    • Helgadottir, Anna
    Publication type:
    Article

  • Genetics of gene expression and its effect on disease.

    Published in:
    Nature, 2008, v. 452, n. 7186, p. 423, doi. 10.1038/nature06758
    By:
    • Emilsson, Valur;
    • Thorleifsson, Gudmar;
    • Bin Zhang;
    • Leonardson, Amy S.;
    • Zink, Florian;
    • Zhu, Jun;
    • Carlson, Sonia;
    • Helgason, Agnar;
    • Walters, G. Bragi;
    • Gunnarsdottir, Steinunn;
    • Mouy, Magali;
    • Steinthorsdottir, Valgerdur;
    • Eiriksdottir, Gudrun H.;
    • Bjornsdottir, Gyda;
    • Reynisdottir, Inga;
    • Gudbjartsson, Daniel;
    • Helgadottir, Anna;
    • Jonasdottir, Aslaug;
    • Jonasdottir, Adalbjorg;
    • Styrkarsdottir, Unnur
    Publication type:
    Article

  • Variants conferring risk of atrial fibrillation on chromosome 4q25.

    Published in:
    Nature, 2007, v. 448, n. 7151, p. 353, doi. 10.1038/nature06007
    By:
    • Gudbjartsson, Daniel F.;
    • Arnar, David O.;
    • Helgadottir, Anna;
    • Gretarsdottir, Solveig;
    • Holm, Hilma;
    • Sigurdsson, Asgeir;
    • Jonasdottir, Adalbjorg;
    • Baker, Adam;
    • Thorleifsson, Gudmar;
    • Kristjansson, Kristleifur;
    • Palsson, Arnar;
    • Blondal, Thorarinn;
    • Sulem, Patrick;
    • Backman, Valgerdur M.;
    • Hardarson, Gudmundur A.;
    • Palsdottir, Ebba;
    • Helgason, Agnar;
    • Sigurjonsdottir, Runa;
    • Sverrisson, Jon T.;
    • Kostulas, Konstantinos
    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 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

  • Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.

    Published in:
    Nature Genetics, 2009, v. 41, n. 3, p. 342, doi. 10.1038/ng.323
    By:
    • Gudbjartsson, DanielF.;
    • Bjornsdottir, Unnur S.;
    • Halapi, Eva;
    • Helgadottir, Anna;
    • Sulem, Patrick;
    • Jonsdottir, Gudrun M.;
    • Thorleifsson, Gudmar;
    • Helgadottir, Hafdis;
    • Steinthorsdottir, Valgerdur;
    • Stefansson, Hreinn;
    • Williams, Carolyn;
    • Hui, Jennie;
    • Beilby, John;
    • Warrington, Nicole M.;
    • James, Alan;
    • Palmer, Lyle J.;
    • Koppelman, Gerard H.;
    • Heinzmann, Andrea;
    • Krueger, Marcus;
    • Boezen, H. Marike
    Publication type:
    Article

  • Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
    By:
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Gudbjartsson, Daniel F.;
    • Steinthorsdottir, Valgerdur;
    • Sulem, Patrick;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Gretarsdottir, Solveig;
    • Thorlacius, Steinunn;
    • Jonsdottir, Ingileif;
    • Jonsdottir, Thorbjorg;
    • Olafsdottir, Elinborg J.;
    • Olafsdottir, Gudridur H.;
    • Jonsson, Thorvaldur;
    • Jonsson, Frosti;
    • Borch-Johnsen, Knut;
    • Hansen, Torben;
    • Andersen, Gitte;
    • Jorgensen, Torben;
    • Lauritzen, Torsten
    Publication type:
    Article

  • Many sequence variants affecting diversity of adult human height.

    Published in:
    Nature Genetics, 2008, v. 40, n. 5, p. 609, doi. 10.1038/ng.122
    By:
    • Gudbjartsson, Daniel F.;
    • Walters, G. Bragi;
    • Thorleifsson, Gudmar;
    • Stefansson, Hreinn;
    • Halldorsson, Bjarni V.;
    • Zusmanovich, Pasha;
    • Sulem, Patrick;
    • Thorlacius, Steinunn;
    • Gylfason, Arnaldur;
    • Steinberg, Stacy;
    • Helgadottir, Anna;
    • Ingason, Andres;
    • Steinthorsdottir, Valgerdur;
    • Olafsdottir, Elinborg J.;
    • Olafsdottir, Gudridur H.;
    • Jonsson, Thorvaldur;
    • Borch-Johnsen, Knut;
    • Hansen, Torben;
    • Andersen, Gitte;
    • Jorgensen, Torben
    Publication type:
    Article

  • The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.

    Published in:
    Nature Genetics, 2008, v. 40, n. 2, p. 217, doi. 10.1038/ng.72
    By:
    • Helgadottir, Anna;
    • Thorleifsson, Gudmar;
    • Magnusson, Kristinn P.;
    • Grétarsdottir, Solveig;
    • Steinthorsdottir, Valgerdur;
    • Manolescu, Andrei;
    • Jones, Gregory T.;
    • Rinkel, Gabriel J. E.;
    • Blankensteijn, Jan D.;
    • Ronkainen, Antti;
    • Jääskeläinen, Juha E.;
    • Kyo, Yoshiki;
    • Lenk, Guy M.;
    • Sakalihasan, Natzi;
    • Kostulas, Konstantinos;
    • Gottsäter, Anders;
    • Flex, Andrea;
    • Stefansson, Hreinn;
    • Hansen, Torben;
    • Andersen, Gitte
    Publication type:
    Article

  • Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 320, doi. 10.1038/ng1732
    By:
    • Grant, Struan F. A.;
    • Thorleifsson, Gudmar;
    • Reynisdottir, Inga;
    • Benediktsson, Rafn;
    • Manolescu, Andrei;
    • Sainz, Jesus;
    • Helgason, Agnar;
    • Stefansson, Hreinn;
    • Emilsson, Valur;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Magnusson, Kristinn P.;
    • Walters, G. Bragi;
    • Palsdottir, Ebba;
    • Jonsdottir, Thorbjorg;
    • Gudmundsdottir, Thorunn;
    • Gylfason, Arnaldur;
    • Saemundsdottir, Jona;
    • Wilensky, Robert L.;
    • Reilly, Muredach P.
    Publication type:
    Article

  • A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.

    Published in:
    Nature Genetics, 2006, v. 38, n. 1, p. 68, doi. 10.1038/ng1692
    By:
    • Helgadottir, Anna;
    • Manolescu, Andrei;
    • Helgason, Agnar;
    • Thorleifsson, Gudmar;
    • Thorsteinsdottir, Unnur;
    • Gudbjartsson, Daniel F;
    • Gretarsdottir, Solveig;
    • Magnusson, Kristinn P;
    • Gudmundsson, Gudmundur;
    • Hicks, Andrew;
    • Jonsson, Thorlakur;
    • Grant, Struan F A;
    • Sainz, Jesus;
    • O'Brien, Stephen J;
    • Sveinbjornsdottir, Sigurlaug;
    • Valdimarsson, Einar M;
    • Matthiasson, Stefan E;
    • Levey, Allan I;
    • Abramson, Jerome L;
    • Reilly, Murdach P
    Publication type:
    Article

  • The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.

    Published in:
    Nature Genetics, 2004, v. 36, n. 3, p. 233, doi. 10.1038/ng1311
    By:
    • Helgadottir, Anna;
    • Manolescu, Andrei;
    • Thorleifsson, Gudmar;
    • Gretarsdottir, Solveig;
    • Jonsdottir, Helga;
    • Thorsteinsdottir, Unnur;
    • Samani, Nilesh J.;
    • Gudmundsson, Gudmundur;
    • A. Grant, Struan F.;
    • Thorgeirsson, Gudmundur;
    • Sveinbjornsdottir, Sigurlaug;
    • Valdimarsson, Einar M.;
    • Matthiasson, Stefan E.;
    • Johannsson, Halldor;
    • Gudmundsdottir, Olof;
    • Gurney, Mark E.;
    • Sainz, Jesus;
    • Thorhallsdottir, Margret;
    • Andresdottir, Margret;
    • Frigge, Michael L.
    Publication type:
    Article

  • A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 9, p. 1, doi. 10.1371/journal.pgen.1005379
    By:
    • Gretarsdottir, Solveig;
    • Helgason, Hannes;
    • Helgadottir, Anna;
    • Sigurdsson, Asgeir;
    • Thorleifsson, Gudmar;
    • Magnusdottir, Audur;
    • Oddsson, Asmundur;
    • Steinthorsdottir, Valgerdur;
    • Rafnar, Thorunn;
    • de Graaf, Jacqueline;
    • Daneshpour, Maryam S.;
    • Hedayati, Mehdi;
    • Azizi, Fereidoun;
    • Grarup, Niels;
    • Jørgensen, Torben;
    • Vestergaard, Henrik;
    • Hansen, Torben;
    • Eyjolfsson, Gudmundur;
    • Sigurdardottir, Olof;
    • Olafsson, Isleifur
    Publication type:
    Article

  • A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09719-4
    By:
    • Bjornsdottir, Gyda;
    • Ivarsdottir, Erna V.;
    • Bjarnadottir, Kristbjorg;
    • Benonisdottir, Stefania;
    • Gylfadottir, Sandra Sif;
    • Arnadottir, Gudny A.;
    • Benediktsson, Rafn;
    • Halldorsson, Gisli Hreinn;
    • Helgadottir, Anna;
    • Jonasdottir, Adalbjorg;
    • Jonasdottir, Aslaug;
    • Jonsdottir, Ingileif;
    • Kristinsdottir, Anna Margret;
    • Magnusson, Olafur Th.;
    • Masson, Gisli;
    • Melsted, Pall;
    • Rafnar, Thorunn;
    • Sigurdsson, Asgeir;
    • Sigurdsson, Gunnar;
    • Skuladottir, Astros
    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

  • Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.

    Published in:
    European Heart Journal, 2023, v. 44, n. 21, p. 1927, doi. 10.1093/eurheartj/ehad142
    By:
    • Chen, Hao Yu;
    • Dina, Christian;
    • Small, Aeron M;
    • Shaffer, Christian M;
    • Levinson, Rebecca T;
    • Helgadóttir, Anna;
    • Capoulade, Romain;
    • Munter, Hans Markus;
    • Martinsson, Andreas;
    • Cairns, Benjamin J;
    • Trudsø, Linea C;
    • Hoekstra, Mary;
    • Burr, Hannah A;
    • Marsh, Thomas W;
    • Damrauer, Scott M;
    • Dufresne, Line;
    • Scouarnec, Solena Le;
    • Messika-Zeitoun, David;
    • Ranatunga, Dilrini K;
    • Whitmer, Rachel A
    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

  • Thiopurine Enhanced ALL Maintenance (TEAM): study protocol for a randomized study to evaluate the improvement in disease-free survival by adding very low dose 6-thioguanine to 6-mercaptopurine/methotrexate-based maintenance therapy in pediatric and adult patients (0-45 years) with newly diagnosed B-cell precursor or T-cell acute lymphoblastic leukemia treated according to the intermediate risk-high group of the ALLTogether1 protocol.

    Published in:
    2022
    By:
    • Toksvang, Linea Natalie;
    • Als-Nielsen, Bodil;
    • Bacon, Christopher;
    • Bertasiute, Ruta;
    • Duarte, Ximo;
    • Escherich, Gabriele;
    • Helgadottir, Elín Anna;
    • Johannsdottir, Inga Rinvoll;
    • Jónsson, Ólafur G.;
    • Kozlowski, Piotr;
    • Langenskjöld, Cecilia;
    • Lepik, Kristi;
    • Niinimäki, Riitta;
    • Overgaard, Ulrik Malthe;
    • Punab, Mari;
    • Räty, Riikka;
    • Segers, Heidi;
    • van der Sluis, Inge;
    • Smith, Owen Patrick;
    • Strullu, Marion
    Publication type:
    journal article

  • Genetic variants associated with platelet count are predictive of human disease and physiological markers.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02642-9
    By:
    • Mikaelsdottir, Evgenia;
    • Thorleifsson, Gudmar;
    • Stefansdottir, Lilja;
    • Halldorsson, Gisli;
    • Sigurdsson, Jon K.;
    • Lund, Sigrun H.;
    • Tragante, Vinicius;
    • Melsted, Pall;
    • Rognvaldsson, Solvi;
    • Norland, Kristjan;
    • Helgadottir, Anna;
    • Magnusson, Magnus K.;
    • Ragnarsson, Gunnar B.;
    • Kristinsson, Sigurdur Y.;
    • Reykdal, Sigrun;
    • Vidarsson, Brynjar;
    • Gudmundsdottir, Ingibjorg J.;
    • Olafsson, Isleifur;
    • Onundarson, Pall T.;
    • Sigurdardottir, Olof
    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 and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-13690-5
    By:
    • Shah, Sonia;
    • Henry, Albert;
    • Roselli, Carolina;
    • Lin, Honghuang;
    • Sveinbjörnsson, Garðar;
    • Fatemifar, Ghazaleh;
    • Hedman, Åsa K.;
    • Wilk, Jemma B.;
    • Morley, Michael P.;
    • Chaffin, Mark D.;
    • Helgadottir, Anna;
    • Verweij, Niek;
    • Dehghan, Abbas;
    • Almgren, Peter;
    • Andersson, Charlotte;
    • Aragam, Krishna G.;
    • Ärnlöv, Johan;
    • Backman, Joshua D.;
    • Biggs, Mary L.;
    • Bloom, Heather L.
    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:
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    • Stephensen, Sigurdur S.;
    • Oskarsson, Gylfi;
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    • Andersen, Karl;
    • Danielsen, Ragnar;
    • Thorgeirsson, Gudmundur;
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  • A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

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    By:
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    • Jonasdottir, Adalbjorg;
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    • Thorleifsson, Gudmar;
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    • Zink, Florian;
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    • Asgeirsdottir, Margret;
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    • Kiemeney, Lambertus A.;
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    Published in:
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    By:
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  • 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;
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    • 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;
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  • 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;
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    • Sveinbjornsson, Gardar;
    • Sulem, Patrick;
    • Norddahl, Gudmundur L;
    • Helgadottir, Anna;
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    • Magnusdottir, Audur;
    • Danielsen, Ragnar;
    • Sigurdsson, Emil L
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  • 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;
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    • Thorleifsson, Gudmar;
    • Jensson, Brynjar Ö;
    • Arnadottir, Gudny A;
    • Olafsson, Isleifur;
    • Eyjolfsson, Gudmundur I;
    • Sigurdardottir, Olof
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  • Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.

    Published in:
    Annals of Neurology, 2008, v. 64, n. 4, p. 402, doi. 10.1002/ana.21480
    By:
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    • Manolescu, Andrei;
    • Styrkarsdottir, Unnur;
    • Helgadottir, Anna;
    • Gschwendtner, Andreas;
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    • Bevan, Steve;
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    • Valdimarsson, Einar Mar;
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  • The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.

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    By:
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    • Holm, Hilma;
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    • Stefansson, Kari;
    • Waddy, Salina;
    • Vaccarino, Viola;
    • Zafari, A. Maziar;
    • Quyyumi, Arshed A.
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