Works by Steinthorsdottir, Valgerdur

Results: 42
    1

    Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-024-55761-2
    By:
    • Kentistou, Katherine A.;
    • Lim, Brandon E. M.;
    • Kaisinger, Lena R.;
    • Steinthorsdottir, Valgerdur;
    • Sharp, Luke N.;
    • Patel, Kashyap A.;
    • Tragante, Vinicius;
    • Hawkes, Gareth;
    • Gardner, Eugene J.;
    • Olafsdottir, Thorhildur;
    • Wood, Andrew R.;
    • Zhao, Yajie;
    • Thorleifsson, Gudmar;
    • Day, Felix R.;
    • Ozanne, Susan E.;
    • Hattersley, Andrew T.;
    • O'Rahilly, Stephen;
    • Stefansson, Kari;
    • Ong, Ken K.;
    • Beaumont, Robin N.
    Publication type:
    Article
    2

    Sequence variants associated with BMI affect disease risk through BMI itself.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-53568-9
    By:
    • Einarsson, Gudmundur;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Zink, Florian;
    • Helgason, Hannes;
    • Olafsdottir, Thorhildur;
    • Rognvaldsson, Solvi;
    • Tragante, Vinicius;
    • Ulfarsson, Magnus O.;
    • Sveinbjornsson, Gardar;
    • Snaebjarnarson, Audunn S.;
    • Einarsson, Hafsteinn;
    • Aegisdottir, Hildur M.;
    • Jonsdottir, Gudrun A.;
    • Helgadottir, Anna;
    • Gretarsdottir, Solveig;
    • Styrkarsdottir, Unnur;
    • Arnason, Hannes K.;
    • Bjarnason, Ragnar;
    • Sigurdsson, Emil
    Publication type:
    Article
    3

    InterPregGen: genetic studies of pre-eclampsia in three continents.

    Published in:
    Norsk Epidemiologi, 2014, v. 24, n. 1/2, p. 141, doi. 10.5324/nje.v24i1-2.1815
    By:
    • Morgan, Linda;
    • McGinnis, Ralph;
    • Steinthorsdottir, Valgerdur;
    • Svyatova, Gulnara;
    • Zakhidova, Nodira;
    • Wai Kwong Lee;
    • Iversen, Ann-Charlotte;
    • Magnus, Per;
    • Walker, James;
    • Casas, Juan Pablo;
    • Sultanov, Saidazim;
    • Laivuori, Hannele
    Publication type:
    Article
    4

    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
    5

    Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.

    Published in:
    Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1081741
    By:
    • Uglebjerg, Nicoline;
    • Ahmadizar, Fariba;
    • Aly, Dina M.;
    • Cañadas-Garre, Marisa;
    • Hill, Claire;
    • Naber, Annemieke;
    • Oddsson, Asmundur;
    • Singh, Sunny S.;
    • Smyth, Laura;
    • Tre´gouët, David-Alexandre;
    • Chaker, Layal;
    • Ghanbari, Mohsen;
    • Steinthorsdottir, Valgerdur;
    • Ahlqvist, Emma;
    • Hadjadj, Samy;
    • Hoek, Mandy Van;
    • Kavousi, Maryam;
    • McKnight, Amy Jayne;
    • Sijbrands, Eric J.;
    • Stefansson, Kari
    Publication type:
    Article
    6

    Evaluating differences in linkage disequilibrium between populations.

    Published in:
    Annals of Human Genetics, 2010, v. 74, n. 3, p. 233, doi. 10.1111/j.1469-1809.2010.00571.x
    By:
    • Hrafnkelsson, Birgir;
    • Helgason, Agnar;
    • Jonsson, Gudbjorn F.;
    • Gudbjartsson, Daniel F.;
    • Jonsson, Thorlakur;
    • Thorvaldsson, Sverrir;
    • Stefansson, Hreinn;
    • Steinthorsdottir, Valgerdur;
    • Vidarsdottir, Nanna;
    • Middleton, Derek;
    • Petersen, Henning S.;
    • Martinez, Conrado;
    • Snaedal, Jon;
    • Jonsson, Palmi V.;
    • Bjornsson, Sigurbjorn;
    • Gulcher, Jeffrey R.;
    • Stefansson, Kari
    Publication type:
    Article
    7

    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 981, doi. 10.1038/ng.2383
    By:
    • Morris, Andrew P;
    • Voight, Benjamin F;
    • Teslovich, Tanya M;
    • Ferreira, Teresa;
    • Segrè, Ayellet V;
    • Steinthorsdottir, Valgerdur;
    • Strawbridge, Rona J;
    • Khan, Hassan;
    • Grallert, Harald;
    • Mahajan, Anubha;
    • Prokopenko, Inga;
    • Kang, Hyun Min;
    • Dina, Christian;
    • Esko, Tonu;
    • Fraser, Ross M;
    • Kanoni, Stavroula;
    • Kumar, Ashish;
    • Lagou, Vasiliki;
    • Langenberg, Claudia;
    • Luan, Jian'an
    Publication type:
    Article
    8

    Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

    Published in:
    2011
    By:
    • Heid, Iris M;
    • Jackson, Anne U;
    • Randall, Joshua C;
    • Winkler, Thomas W;
    • Qi, Lu;
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Zillikens, M Carola;
    • Speliotes, Elizabeth K;
    • Mägi, Reedik;
    • Workalemahu, Tsegaselassie;
    • White, Charles C;
    • Bouatia-Naji, Nabila;
    • Harris, Tamara B;
    • Berndt, Sonja I;
    • Ingelsson, Erik;
    • Willer, Cristen J;
    • Weedon, Michael N;
    • Luan, Jian'an;
    • Vedantam, Sailaja
    Publication type:
    Correction Notice
    9

    Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

    Published in:
    2011
    By:
    • Voight, Benjamin F.;
    • Scott, Laura J.;
    • Steinthorsdottir, Valgerdur;
    • Morris, Andrew P.;
    • Dina, Christian;
    • Welch, Ryan P.;
    • Zeggini, Eleftheria;
    • Huth, Cornelia;
    • Aulchenko, Yurii S.;
    • Thorleifsson, Gudmar;
    • McCulloch, Laura J.;
    • Ferreira, Teresa;
    • Grallert, Harald;
    • Amin, Najaf;
    • Wu, Guanming;
    • Willer, Cristen J.;
    • Raychaudhuri, Soumya;
    • McCarroll, Steve A.;
    • Langenberg, Claudia;
    • Hofmann, Oliver M.
    Publication type:
    Correction Notice
    10

    Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

    Published in:
    Nature Genetics, 2010, v. 42, n. 11, p. 937, doi. 10.1038/ng.686
    By:
    • Speliotes, Elizabeth K.;
    • Willer, Cristen J.;
    • Berndt, Sonja I.;
    • Monda, Keri L.;
    • Thorleifsson, Gudmar;
    • Jackson, Anne U.;
    • Allen, Hana Lango;
    • Lindgren, Cecilia M.;
    • Luan, Jian'an;
    • Mägi, Reedik;
    • Randall, Joshua C.;
    • Vedantam, Sailaja;
    • Winkler, Thomas W.;
    • Lu Qi;
    • Workalemahu, Tsegaselassie;
    • Heid, Iris M.;
    • Steinthorsdottir, Valgerdur;
    • Stringham, Heather M.;
    • Weedon, Michael N.;
    • Wheeler, Eleanor
    Publication type:
    Article
    11

    Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

    Published in:
    Nature Genetics, 2010, v. 42, n. 11, p. 949, doi. 10.1038/ng.685
    By:
    • Heid, Iris M.;
    • Jackson, Anne U.;
    • Randall, Joshua C.;
    • Winkler, Thomas W.;
    • Lu Qi;
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Zillikens, M. Carola;
    • Speliotes, Elizabeth K.;
    • Mägi, Reedik;
    • Workalemahu, Tsegaselassie;
    • White, Charles C.;
    • Bouatia-Naji, Nabila;
    • Harris, Tamara B.;
    • Berndt, Sonja I.;
    • Ingelsson, Erik;
    • Willer, Cristen J.;
    • Weedon, Michael N.;
    • Luan, Jian'an;
    • Vedantam, Sailaja
    Publication type:
    Article
    12

    Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

    Published in:
    Nature Genetics, 2010, v. 42, n. 7, p. 579, doi. 10.1038/ng.609
    By:
    • Voight, Benjamin F;
    • Scott, Laura J;
    • Steinthorsdottir, Valgerdur;
    • Morris, Andrew P;
    • Dina, Christian;
    • Welch, Ryan P;
    • Zeggini, Eleftheria;
    • Huth, Cornelia;
    • Aulchenko, Yurii S;
    • Thorleifsson, Gudmar;
    • McCulloch, Laura J;
    • Ferreira, Teresa;
    • Grallert, Harald;
    • Amin, Najaf;
    • Wu, Guanming;
    • Willer, Cristen J;
    • Raychaudhuri, Soumya;
    • McCarroll, Steve A;
    • Langenberg, Claudia;
    • Hofmann, Oliver M
    Publication type:
    Article
    13

    Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

    Published in:
    2010
    By:
    • Dupuis, Josée;
    • Langenberg, Claudia;
    • Prokopenko, Inga;
    • Saxena, Richa;
    • Soranzo, Nicole;
    • Jackson, Anne U;
    • Wheeler, Eleanor;
    • Glazer, Nicole L;
    • Bouatia-Naji, Nabila;
    • Gloyn, Anna L;
    • Lindgren, Cecilia M;
    • Mägi, Reedik;
    • Morris, Andrew P;
    • Randall, Joshua;
    • Johnson, Toby;
    • Elliott, Paul;
    • Rybin, Denis;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Henneman, Peter
    Publication type:
    Correction Notice
    14

    New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 105, doi. 10.1038/ng.520
    By:
    • Dupuis, Josée;
    • Langenberg, Claudia;
    • Prokopenko, Inga;
    • Saxena, Richa;
    • Soranzo, Nicole;
    • Jackson, Anne U.;
    • Wheeler, Eleanor;
    • Glazer, Nicole L.;
    • Bouatia-Naji, Nabila;
    • Gloyn, Anna L.;
    • Lindgren, Cecilia M.;
    • Mägi, Reedik;
    • Morris, Andrew P.;
    • Randall, Joshua;
    • Johnson, Toby;
    • Elliott, Paul;
    • Rybin, Denis;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Henneman, Peter
    Publication type:
    Article
    15

    Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.

    Published in:
    Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
    By:
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F.;
    • Rafnar, Thorunn;
    • Holm, Hilma;
    • Olafsdottir, Elinborg J.;
    • Olafsdottir, Gudridur H.;
    • Jonsson, Thorvaldur;
    • Alexandersen, Peter;
    • Feenstra, Bjarke;
    • Boyd, Heather A.;
    • Aben, Katja K.;
    • Verbeek, Andre L. M.;
    • Roeleveld, Nel;
    • Jonasdottir, Aslaug;
    • Styrkarsdottir, Unnur;
    • Steinthorsdottir, Valgerdur;
    • Karason, Ari;
    • Stacey, Simon N.;
    • Gudmundsson, Julius;
    • Jakobsdottir, Margret
    Publication type:
    Article
    16

    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
    17

    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
    18

    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
    19

    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
    20

    Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 977, doi. 10.1038/ng2062
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Steinthorsdottir, Valgerdur;
    • Bergthorsson, Jon T.;
    • Thorleifsson, Gudmar;
    • Manolescu, Andrei;
    • Rafnar, Thorunn;
    • Gudbjartsson, Daniel;
    • Agnarsson, Bjarni A.;
    • Baker, Adam;
    • Sigurdsson, Asgeir;
    • Benediktsdottir, Kristrun R.;
    • Jakobsdottir, Margret;
    • Thorarinn Blondal1,;
    • Stacey, Simon N.;
    • Helgason, Agnar;
    • Gunnarsdottir, Steinunn;
    • Olafsdottir, Adalheidur;
    • Kristinsson, Kari T.;
    • Birgisdottir, Birgitta
    Publication type:
    Article
    21

    A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.

    Published in:
    Nature Genetics, 2007, v. 39, n. 6, p. 770, doi. 10.1038/ng2043
    By:
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Reynisdottir, Inga;
    • Benediktsson, Rafn;
    • Jonsdottir, Thorbjorg;
    • Walters, G. Bragi;
    • Styrkarsdottir, Unnur;
    • Gretarsdottir, Solveig;
    • Emilsson, Valur;
    • Ghosh, Shyamali;
    • Baker, Adam;
    • Snorradottir, Steinunn;
    • Bjarnason, Hjordis;
    • Ng, Maggie C. Y.;
    • Hansen, Torben;
    • Bagger, Yu;
    • Wilensky, Robert L.;
    • Reilly, Muredach P.;
    • Adeyemo, Adebowale;
    • Yuanxiu Chen
    Publication type:
    Article
    22

    A common inversion under selection in Europeans.

    Published in:
    Nature Genetics, 2005, v. 37, n. 2, p. 129, doi. 10.1038/ng1508
    By:
    • Stefansson, Hreinn;
    • Helgason, Agnar;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Masson, Gisli;
    • Barnard, John;
    • Baker, Adam;
    • Jonasdottir, Aslaug;
    • Ingason, Andres;
    • Gudnadottir, Vala G.;
    • Desnica, Natasa;
    • Hicks, Andrew;
    • Gylfason, Arnaldur;
    • Gudbjartsson, Daniel F.;
    • Jonsdottir, Gudrun M.;
    • Sainz, Jesus;
    • Agnarsson, Kari;
    • Birgisdottir, Birgitta;
    • Ghosh, Shyamali;
    • Olafsdottir, Adalheidur
    Publication type:
    Article
    23

    Genetic Architecture of Vitamin B<sub>12</sub> and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003530
    By:
    • Grarup, Niels;
    • Sulem, Patrick;
    • Sandholt, Camilla H.;
    • Thorleifsson, Gudmar;
    • Ahluwalia, Tarunveer S.;
    • Steinthorsdottir, Valgerdur;
    • Bjarnason, Helgi;
    • Gudbjartsson, Daniel F.;
    • Magnusson, Olafur T.;
    • Sparsø, Thomas;
    • Albrechtsen, Anders;
    • Kong, Augustine;
    • Masson, Gisli;
    • Tian, Geng;
    • Cao, Hongzhi;
    • Nie, Chao;
    • Kristiansen, Karsten;
    • Husemoen, Lise Lotte;
    • Thuesen, Betina;
    • Li, Yingrui
    Publication type:
    Article
    24

    Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002741
    By:
    • Perry, John R. B.;
    • Voight, Benjamin F.;
    • Yengo, Loïc;
    • Amin, Najaf;
    • Dupuis, Josée;
    • Ganser, Martha;
    • Grallert, Harald;
    • Navarro, Pau;
    • Man Li;
    • Lu Qi;
    • Steinthorsdottir, Valgerdur;
    • Scott, Robert A.;
    • Almgren, Peter;
    • Arking, Dan E.;
    • Aulchenko, Yurii;
    • Balkau, Beverley;
    • Benediktsson, Rafn;
    • Bergman, Richard N.;
    • Boerwinkle, Eric;
    • Bonnycastle, Lori
    Publication type:
    Article
    25

    Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.

    Published in:
    Nature Genetics, 2014, v. 46, n. 3, p. 294, doi. 10.1038/ng.2882
    By:
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Helgason, Hannes;
    • Grarup, Niels;
    • Sigurdsson, Asgeir;
    • Helgadottir, Hafdis T;
    • Johannsdottir, Hrefna;
    • Magnusson, Olafur T;
    • Gudjonsson, Sigurjon A;
    • Justesen, Johanne M;
    • Harder, Marie N;
    • Jørgensen, Marit E;
    • Christensen, Cramer;
    • Brandslund, Ivan;
    • Sandbæk, Annelli;
    • Lauritzen, Torsten;
    • Vestergaard, Henrik;
    • Linneberg, Allan;
    • Jørgensen, Torben
    Publication type:
    Article
    26

    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
    27

    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;
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    • Tragante, Vinicius;
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    Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

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    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38951-2
    By:
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    • 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
    29

    Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.

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    Nature Communications, 2017, v. 8, n. 5, p. 15539, doi. 10.1038/ncomms15539
    By:
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    • Morris, Andrew P.;
    • Fassbender, Amelie;
    • Rahmioglu, Nilufer;
    • De Vivo, Immaculata;
    • Buring, Julie E.;
    • Zhang, Futao;
    • Edwards, Todd L.;
    • Jones, Sarah;
    • O, Dorien;
    • Peterse, Daniëlle;
    • Rexrode, Kathryn M.;
    • Ridker, Paul M.;
    • Schork, Andrew J.;
    • MacGregor, Stuart;
    • Martin, Nicholas G.;
    • Becker, Christian M.;
    • Adachi, Sosuke;
    • Yoshihara, Kosuke
    Publication type:
    Article
    30

    Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.

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    Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
    By:
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    • Thorleifsson, Gudmar;
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    • Feenstra, Bjarke;
    • Sigurdsson, Asgeir;
    • Stefansdottir, Lilja;
    • Kristinsdottir, Anna M.;
    • Zink, Florian;
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    • Munk Nielsen, Nete;
    • Geller, Frank;
    • Melbye, Mads;
    • Gudbjartsson, Daniel F.;
    • Geirsson, Reynir T.;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article
    31
    32

    Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.

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    Human Genetics, 2021, v. 140, n. 3, p. 529, doi. 10.1007/s00439-020-02223-6
    By:
    • Adewuyi, Emmanuel O.;
    • Mehta, Divya;
    • Sapkota, Yadav;
    • International Endogene Consortium;
    • Yoshihara, Kosuke;
    • Nyegaard, Mette;
    • Steinthorsdottir, Valgerdur;
    • Morris, Andrew P.;
    • Fassbender, Amelie;
    • Rahmioglu, Nilufer;
    • De Vivo, Immaculata;
    • Buring, Julie E.;
    • Zhang, Futao;
    • Edwards, Todd L.;
    • Jones, Sarah;
    • Dorien;
    • Peterse, Daniëlle;
    • Rexrode, Kathryn M.;
    • Ridker, Paul M.;
    • Schork, Andrew J.
    Publication type:
    Article
    33
    34

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

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    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05428-6
    By:
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    • 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;
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    • Davidsson, Olafur B.
    Publication type:
    Article
    35

    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.

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    • Scott, Laura J.;
    • Mägi, Reedik;
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    • Johnson, Andrew D.;
    • Eicher, John D.;
    • Jackson, Anne U.;
    • Ferreira, Teresa;
    • Yeji Lee;
    • Ma, Clement;
    • Steinthorsdottir, Valgerdur;
    • Thorleifsson, Gudmar;
    • Lu Qi;
    • Van Zuydam, Natalie R.;
    • Mahajan, Anubha;
    • Chen, Han
    Publication type:
    journal article
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    Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion.

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    Diabetes, 2015, v. 64, n. 6, p. 2279, doi. 10.2337/db14-1456
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    • Vangipurapu, Jagadish;
    • Weedon, Michael N.;
    • Weijia Xie;
    • Wood, Andrew R.;
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    • Mari, Andrea;
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    • Lawlor, Debbie A.;
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    • Steinthorsdottir, Valgerdur;
    • Guðbjartsson, Daniel F.;
    • Thorleifsson, Gudmar;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
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    37

    Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.

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    Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19733-6
    By:
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    • McGinnis, Ralph;
    • Williams, Nicholas O.;
    • Stefansdottir, Lilja;
    • Thorleifsson, Gudmar;
    • Shooter, Scott;
    • Fadista, João;
    • Sigurdsson, Jon K.;
    • Auro, Kirsi M.;
    • Berezina, Galina;
    • Borges, Maria-Carolina;
    • Bumpstead, Suzannah;
    • Bybjerg-Grauholm, Jonas;
    • Colgiu, Irina;
    • Dolby, Vivien A.;
    • Dudbridge, Frank;
    • Engel, Stephanie M.;
    • Franklin, Christopher S.;
    • Frigge, Michael L.;
    • Frisbaek, Yr
    Publication type:
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    38

    FTO genotype is associated with phenotypic variability of body mass index.

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    Nature, 2012, v. 490, n. 7419, p. 267, doi. 10.1038/nature11401
    By:
    • Yang, Jian;
    • Loos, Ruth J. F.;
    • Powell, Joseph E.;
    • Medland, Sarah E.;
    • Speliotes, Elizabeth K.;
    • Chasman, Daniel I.;
    • Rose, Lynda M.;
    • Thorleifsson, Gudmar;
    • Steinthorsdottir, Valgerdur;
    • Mägi, Reedik;
    • Waite, Lindsay;
    • Vernon Smith, Albert;
    • Yerges-Armstrong, Laura M.;
    • Monda, Keri L.;
    • Hadley, David;
    • Mahajan, Anubha;
    • Li, Guo;
    • Kapur, Karen;
    • Vitart, Veronique;
    • Huffman, Jennifer E.
    Publication type:
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    39

    Parental origin of sequence variants associated with complex diseases.

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    Nature, 2009, v. 462, n. 7275, p. 868, doi. 10.1038/nature08625
    By:
    • Kong, Augustine;
    • Steinthorsdottir, Valgerdur;
    • Masson, Gisli;
    • Thorleifsson, Gudmar;
    • Sulem, Patrick;
    • Besenbacher, Soren;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Kristinsson, Kari Th.;
    • Jonasdottir, Adalbjorg;
    • Frigge, Michael L.;
    • Gylfason, Arnaldur;
    • Olason, Pall I.;
    • Gudjonsson, Sigurjon A.;
    • Sverrisson, Sverrir;
    • Stacey, Simon N.;
    • Sigurgeirsson, Bardur;
    • Benediktsdottir, Kristrun R.;
    • Sigurdsson, Helgi;
    • Jonsson, Thorvaldur
    Publication type:
    Article
    40

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

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    European Heart Journal, 2020, v. 41, n. 28, p. 2618, doi. 10.1093/eurheartj/ehaa531
    By:
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    • 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;
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    • Pedersen, Ole B
    Publication type:
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    Sequence variants associating with urinary biomarkers.

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    Human Molecular Genetics, 2019, v. 28, n. 7, p. 1199, doi. 10.1093/hmg/ddy409
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    • 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;
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    • Asselbergs, Folkert W
    Publication type:
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    42

    Neuregulin 1 and schizophrenia.

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    Annals of Medicine, 2004, v. 36, n. 1, p. 62, doi. 10.1080/07853890310017585
    By:
    • Stefansson, Hreinn;
    • Steinthorsdottir, Valgerdur;
    • Thorgeirsson, Thorgeir E.;
    • Gulcher, Jeffrey R.;
    • Stefansson, Kari
    Publication type:
    Article