Found: 59

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  • Addictions and their familiality in Iceland.

    Published in:
    Annals of the New York Academy of Sciences, 2010, v. 1187, n. 1, p. 208, doi. 10.1111/j.1749-6632.2009.05151.x
    By:
    • Tyrfingsson, Thorarinn;
    • Thorgeirsson, Thorgeir E.;
    • Geller, Frank;
    • Runarsdóttir, Valgerdur;
    • Hansdóttir, Ingunn;
    • Bjornsdottir, Gyda;
    • Wiste, Anna K.;
    • Jonsdottir, Gudrun A.;
    • Stefansson, Hreinn;
    • Gulcher, Jeffrey R.;
    • Oskarsson, Hogni;
    • Gudbjartsson, Daniel;
    • Stefansson, Kari
    Publication type:
    Article

  • A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 2, p. 562
    By:
    • Holmans, Peter;
    • Moskvina, Valentina;
    • Jones, Lesley;
    • Sharma, Manu;
    • Vedernikov, Alexey;
    • Buchel, Finja;
    • Saad, Mohamad;
    • Bras, Jose M.;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Durr, Alexandra;
    • Guerreiro, Rita;
    • Hernandez, Dena;
    • Brice, Alexis;
    • Stefánsson, Hreinn;
    • Majamaa, Kari
    Publication type:
    Article

  • Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2973
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • chel, Finja Bü;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article

  • Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 8, p. 1696
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Büchel, Finja;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article

  • A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 5, p. 1039
    By:
    • Holmans, Peter;
    • Moskvina, Valentina;
    • Jones, Lesley;
    • Sharma, Manu;
    • Vedernikov, Alexey;
    • Buchel, Finja;
    • Sadd, Mohamad;
    • Bras, Jose M.;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Durr, Alexandra;
    • Guerreiro, Rita;
    • Hernandez, Dena;
    • Brice, Alexis;
    • Stefánsson, Hreinn;
    • Majamaa, Kari
    Publication type:
    Article

  • Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 22, p. 4996
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Büchel, Finja;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article

  • A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration).

    Published in:
    Human Molecular Genetics, 2004, v. 13, n. 9, p. 975, doi. 10.1093/hmg/ddh106
    By:
    • Fossdal, Ragnheidur;
    • Jonasson, Fridbert;
    • Kristjansdottir, Gudlaug T.;
    • Kong, Augustine;
    • Stefansson, Hreinn;
    • Gosh, Shyamali;
    • Gulcher, Jeffrey R.;
    • Stefansson, Kari
    Publication type:
    Article

  • Reproductive fitness and genetic risk of psychiatric disorders in the general population.

    Published in:
    Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15833
    By:
    • Mullins, Niamh;
    • Ingason, Andrés;
    • Porter, Heather;
    • Euesden, Jack;
    • Gillett, Alexandra;
    • Ólafsson, Sigurgeir;
    • Gudbjartsson, Daniel F.;
    • Lewis, Cathryn M.;
    • Sigurdsson, Engilbert;
    • Saemundsen, Evald;
    • Gudmundsson, Ólafur Ó.;
    • Frigge, Michael L.;
    • Kong, Augustine;
    • Helgason, Agnar;
    • Walters, G. Bragi;
    • Gustafsson, Omar;
    • Stefansson, Hreinn;
    • Stefansson, Kari
    Publication type:
    Article

  • A mutation in APP protects against Alzheimer's disease and age-related cognitive decline.

    Published in:
    Nature, 2012, v. 488, n. 7409, p. 96, doi. 10.1038/nature11283
    By:
    • Jonsson, Thorlakur;
    • Atwal, Jasvinder K.;
    • Steinberg, Stacy;
    • Snaedal, Jon;
    • Jonsson, Palmi V.;
    • Bjornsson, Sigurbjorn;
    • Stefansson, Hreinn;
    • Sulem, Patrick;
    • Gudbjartsson, Daniel;
    • Maloney, Janice;
    • Hoyte, Kwame;
    • Gustafson, Amy;
    • Liu, Yichin;
    • Lu, Yanmei;
    • Bhangale, Tushar;
    • Graham, Robert R.;
    • Huttenlocher, Johanna;
    • Bjornsdottir, Gyda;
    • Andreassen, Ole A.;
    • Jönsson, Erik G.
    Publication type:
    Article

  • Common variants conferring risk of schizophrenia.

    Published in:
    Nature, 2009, v. 460, n. 7256, p. 744, doi. 10.1038/nature08186
    By:
    • Stefansson, Hreinn;
    • Ophoff, Roel A.;
    • Steinberg, Stacy;
    • Andreassen, Ole A.;
    • Cichon, Sven;
    • Rujescu, Dan;
    • Werge, Thomas;
    • Pietiläinen, Olli P. H.;
    • Mors, Ole;
    • Mortensen, Preben B.;
    • Sigurdsson, Engilbert;
    • Gustafsson, Omar;
    • Nyegaard, Mette;
    • Tuulio-Henriksson, Annamari;
    • Ingason, Andres;
    • Hansen, Thomas;
    • Suvisaari, Jaana;
    • Lonnqvist, Jouko;
    • Paunio, Tiina;
    • Børglum, Anders D.
    Publication type:
    Article

  • Large recurrent microdeletions associated with schizophrenia.

    Published in:
    Nature, 2008, v. 455, n. 7210, p. 232, doi. 10.1038/nature07229
    By:
    • Stefansson, Hreinn;
    • Rujescu, Dan;
    • Cichon, Sven;
    • Pietiläinen, Olli P. H.;
    • Ingason, Andres;
    • Steinberg, Stacy;
    • Fossdal, Ragnheidur;
    • Sigurdsson, Engilbert;
    • Sigmundsson, Thordur;
    • Buizer-Voskamp, Jacobine E.;
    • Hansen, Thomas;
    • Jakobsen, Klaus D.;
    • Muglia, Pierandrea;
    • Francks, Clyde;
    • Matthews, Paul M.;
    • Gylfason, Arnaldur;
    • Halldorsson, Bjarni V.;
    • Gudbjartsson, Daniel;
    • Thorgeirsson, Thorgeir E.;
    • Sigurdsson, Asgeir
    Publication type:
    Article

  • A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.

    Published in:
    Nature, 2008, v. 452, n. 7187, p. 638, doi. 10.1038/nature06846
    By:
    • Thorgeirsson, Thorgeir E.;
    • Geller, Frank;
    • Sulem, Patrick;
    • Rafnar, Thorunn;
    • Wiste, Anna;
    • Magnusson, Kristinn P.;
    • Manolescu, Andrei;
    • Thorleifsson, Gudmar;
    • Stefansson, Hreinn;
    • Ingason, Andres;
    • Stacey, Simon N.;
    • Bergthorsson, Jon T.;
    • Thorlacius, Steinunn;
    • Gudmundsson, Julius;
    • Jonsson, Thorlakur;
    • Jakobsdottir, Margret;
    • Saemundsdottir, Jona;
    • Olafsdottir, Olof;
    • Gudmundsson, Larus J.;
    • Bjornsdottir, Gyda
    Publication type:
    Article

  • DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.

    Published in:
    BMC Genomic Data, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12863-023-01132-7
    By:
    • Banasik, Karina;
    • Møller, Peter L.;
    • Techlo, Tanya R.;
    • Holm, Peter C.;
    • Walters, G. Bragi;
    • Ingason, Andrés;
    • Rosengren, Anders;
    • Rohde, Palle D.;
    • Kogelman, Lisette J. A.;
    • Westergaard, David;
    • Siggaard, Troels;
    • Chmura, Piotr J.;
    • Chalmer, Mona A.;
    • Magnússon, Ólafur Þ.;
    • Þórisson, Guðmundur Á.;
    • Stefánsson, Hreinn;
    • Guðbjartsson, Daníel F.;
    • Stefánsson, Kári;
    • Olesen, Jes;
    • Winther, Simon
    Publication type:
    Article

  • Support for involvement of the AHI1 locus in schizophrenia.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 9, p. 988, doi. 10.1038/sj.ejhg.5201848
    By:
    • Ingason, Andres;
    • Sigmundsson, Thordur;
    • Steinberg, Stacy;
    • Sigurdsson, Engilbert;
    • Haraldsson, Magnus;
    • Magnusdottir, Brynja B.;
    • Frigge, Michael L.;
    • Kong, Augustine;
    • Gulcher, Jeffrey;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari;
    • Petursson, Hannes;
    • Stefansson, Hreinn
    Publication type:
    Article

  • A genome-wide scan for preeclampsia in the Netherlands.

    Published in:
    European Journal of Human Genetics, 2001, v. 9, n. 10, p. 758, doi. 10.1038/sj.ejhg.5200706
    By:
    • Lachmeijer, Augusta MA;
    • Arngrímsson, Reynir;
    • Bastiaans, Esther J;
    • Frigge, Michael L;
    • Pals, Gerald;
    • Sigurdardóttir, Sigrun;
    • Stéfansson, Hreinn;
    • Pálsson, Birgir;
    • Nicolae, Dan;
    • Kong, Augustin;
    • Aarnoudse, Jan G;
    • Gulcher, Jeff R;
    • Dekker, Guustaaf A;
    • ten Kate, Leo P;
    • Stéfansson, Kári
    Publication type:
    Article

  • Identification of a large set of rare complete human knockouts.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 448, doi. 10.1038/ng.3243
    By:
    • Sulem, Patrick;
    • Oddson, Asmundur;
    • Stefansson, Hreinn;
    • Gudjonsson, Sigurjon A;
    • Zink, Florian;
    • Hjartarson, Eirikur;
    • Sigurdsson, Gunnar Th;
    • Jonasdottir, Adalbjorg;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Magnusson, Olafur Th;
    • Masson, Gisli;
    • Helgason, Hannes;
    • Kong, Augustine;
    • Gudbjartsson, Daniel F;
    • Helgason, Agnar;
    • Holm, Hilma;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari
    Publication type:
    Article

  • Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 445, doi. 10.1038/ng.3246
    By:
    • Steinberg, Stacy;
    • Stefansson, Hreinn;
    • Jonsson, Thorlakur;
    • Johannsdottir, Hrefna;
    • Ingason, Andres;
    • Helgason, Hannes;
    • Sulem, Patrick;
    • Magnusson, Olafur Th;
    • Gudjonsson, Sigurjon A;
    • Unnsteinsdottir, Unnur;
    • Kong, Augustine;
    • Westlye, Lars T;
    • Selbæk, Geir;
    • Giegling, Ina;
    • Rujescu, Dan;
    • Hampel, Harald;
    • Hiltunen, Mikko;
    • Andreassen, Ole A;
    • Jonsson, Palmi V;
    • Bjornsson, Sigurbjorn
    Publication type:
    Article

  • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043
    By:
    • Nalls, Mike A;
    • Pankratz, Nathan;
    • Lill, Christina M;
    • Do, Chuong B;
    • Hernandez, Dena G;
    • Saad, Mohamad;
    • DeStefano, Anita L;
    • Kara, Eleanna;
    • Bras, Jose;
    • Sharma, Manu;
    • Schulte, Claudia;
    • Keller, Margaux F;
    • Arepalli, Sampath;
    • Letson, Christopher;
    • Edsall, Connor;
    • Stefansson, Hreinn;
    • Liu, Xinmin;
    • Pliner, Hannah;
    • Lee, Joseph H;
    • Cheng, Rong
    Publication type:
    Article

  • A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1371, doi. 10.1038/ng.2740
    By:
    • Helgason, Hannes;
    • Sulem, Patrick;
    • Duvvari, Maheswara R;
    • Luo, Hongrong;
    • Thorleifsson, Gudmar;
    • Stefansson, Hreinn;
    • Jonsdottir, Ingileif;
    • Masson, Gisli;
    • Gudbjartsson, Daniel F;
    • Walters, G Bragi;
    • Magnusson, Olafur Th;
    • Kong, Augustine;
    • Rafnar, Thorunn;
    • Kiemeney, Lambertus A;
    • Schoenmaker-Koller, Frederieke E;
    • Zhao, Ling;
    • Boon, Camiel J F;
    • Song, Yaojun;
    • Fauser, Sascha;
    • Pei, Michelle
    Publication type:
    Article

  • Identification of low-frequency variants associated with gout and serum uric acid levels.

    Published in:
    Nature Genetics, 2011, v. 43, n. 11, p. 1127, doi. 10.1038/ng.972
    By:
    • Sulem, Patrick;
    • Gudbjartsson, Daniel F;
    • Walters, G Bragi;
    • Helgadottir, Hafdis T;
    • Helgason, Agnar;
    • Gudjonsson, Sigurjon A;
    • Zanon, Carlo;
    • Besenbacher, Soren;
    • Bjornsdottir, Gyda;
    • Magnusson, Olafur T;
    • Magnusson, Gisli;
    • Hjartarson, Eirikur;
    • Saemundsdottir, Jona;
    • Gylfason, Arnaldur;
    • Jonasdottir, Adalbjorg;
    • Holm, Hilma;
    • Karason, Ari;
    • Rafnar, Thorunn;
    • Stefansson, Hreinn;
    • Andreassen, Ole A
    Publication type:
    Article

  • A rare variant in MYH6 is associated with high risk of sick sinus syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 316, doi. 10.1038/ng.781
    By:
    • Holm, Hilma;
    • Gudbjartsson, Daniel F.;
    • Sulem, Patrick;
    • Masson, Gisli;
    • Helgadottir, Hafdis Th;
    • Zanon, Carlo;
    • Magnusson, Olafur Th;
    • Helgason, Agnar;
    • Saemundsdottir, Jona;
    • Gylfason, Arnaldur;
    • Stefansdottir, Hrafnhildur;
    • Gretarsdottir, Solveig;
    • Matthiasson, Stefan E.;
    • Thorgeirsson, Guðmundur;
    • Jonasdottir, Aslaug;
    • Sigurdsson, Asgeir;
    • Stefansson, Hreinn;
    • Werge, Thomas;
    • Rafnar, Thorunn;
    • Kiemeney, Lambertus A.
    Publication type:
    Article

  • Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 906, doi. 10.1038/ng.661
    By:
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Hewitt, Alex W.;
    • Masson, Gisli;
    • Helgason, Agnar;
    • DeWan, Andrew;
    • Sigurdsson, Asgeir;
    • Jonasdottir, Adalbjorg;
    • Gudjonsson, Sigurjon A.;
    • Magnusson, Kristinn P.;
    • Stefansson, Hreinn;
    • Lam, Dennis S. C.;
    • Tam, Pancy O. S.;
    • Gudmundsdottir, Gudrun J.;
    • Southgate, Laura;
    • Burdon, Kathryn P.;
    • Gottfredsdottir, Maria Soffia;
    • Aldred, Micheala A.;
    • Mitchell, Paul;
    • Clair, David St.
    Publication type:
    Article

  • Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 869, doi. 10.1038/ng.652
    By:
    • Anttila, Verneri;
    • Stefansson, Hreinn;
    • Kallela, Mikko;
    • Todt, Unda;
    • Terwindt, Gisela M.;
    • Calafato, M. Stella;
    • Nyholt, Dale R.;
    • Dimas, Antigone S.;
    • Freilinger, Tobias;
    • Müller-Myhsok, Bertram;
    • Artto, Ville;
    • Inouye, Michael;
    • Alakurtti, Kirsi;
    • Kaunisto, Mari A.;
    • Hämäläinen, Eija;
    • de Vries, Boukje;
    • Stam, Anine H.;
    • Weller, Claudia M.;
    • Heinze, Axel;
    • Heinze-Kuhn, Katja
    Publication type:
    Article

  • Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior.

    Published in:
    Nature Genetics, 2010, v. 42, n. 5, p. 448, doi. 10.1038/ng.573
    By:
    • Thorgeirsson, Thorgeir E.;
    • Gudbjartsson, Daniel F.;
    • Surakka, Ida;
    • Vink, Jacqueline M.;
    • Amin, Najaf;
    • Geller, Frank;
    • Sulem, Patrick;
    • Rafnar, Thorunn;
    • Esko, Tõnu;
    • Walter, Stefan;
    • Gieger, Christian;
    • Rawal, Rajesh;
    • Mangino, Massimo;
    • Prokopenko, Inga;
    • Mägi, Reedik;
    • Keskitalo, Kaisu;
    • Gudjonsdottir, Iris H.;
    • Gretarsdottir, Solveig;
    • Stefansson, Hreinn;
    • Thompson, John R.
    Publication type:
    Article

  • Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor.

    Published in:
    2009
    By:
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Petursson, Hjorvar;
    • Gustafsson, Omar;
    • Gudjonsdottir, Iris H;
    • Jonsdottir, Gudrun A;
    • Palsson, Stefan T;
    • Jonsson, Thorlakur;
    • Saemundsdottir, Jona;
    • Bjornsdottir, Gyda;
    • Böttcher, Yvonne;
    • Thorlacius, Theodora;
    • Haubenberger, Dietrich;
    • Zimprich, Alexander;
    • Auff, Eduard;
    • Hotzy, Christoph;
    • Testa, Claudia M;
    • Miyatake, Lisa A;
    • Rosen, Ami R;
    • Kristleifsson, Kristleifur
    Publication type:
    Correction notice

  • Variant in the sequence of the LINGO1 gene confers risk of essential tremor.

    Published in:
    Nature Genetics, 2009, v. 41, n. 3, p. 277, doi. 10.1038/ng.299
    By:
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Petursson, Hjorvar;
    • Gustafsson, Omar;
    • Gudjonsdottir, Iris H.;
    • Jonsdottir, Gudrun A.;
    • Palsson, Stefan T.;
    • Jonsson, Thorlakur;
    • Saemundsdottir, Jona;
    • Bjornsdottir1, Gyda;
    • Böttcher, Yvonne;
    • Thorlacius, Theodora;
    • Haubenberger, Dietrich;
    • Zimprich, Alexander;
    • Auff, Eduard;
    • Hotzy, Christoph;
    • Testa, Claudia M.;
    • Miyatake, Lisa A.;
    • Rosen, Ami R.;
    • Kristleifsson, Kristleifur
    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

  • Male-pattern baldness susceptibility locus at 20p11.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1282, doi. 10.1038/ng.255
    By:
    • Richards, J Brent;
    • Yuan, Xin;
    • Geller, Frank;
    • Waterworth, Dawn;
    • Bataille, Veronique;
    • Glass, Daniel;
    • Song, Kijoung;
    • Waeber, Gerard;
    • Vollenweider, Peter;
    • Aben, Katja K H;
    • Kiemeney, Lambertus A;
    • Walters, Bragi;
    • Soranzo, Nicole;
    • Thorsteinsdottir, Unnur;
    • Kong, Augustine;
    • Rafnar, Thorunn;
    • Deloukas, Panos;
    • Sulem, Patrick;
    • Stefansson, Hreinn;
    • Stefansson, Kari
    Publication type:
    Article

  • Detection of sharing by descent, long-range phasing and haplotype imputation.

    Published in:
    Nature Genetics, 2008, v. 40, n. 9, p. 1068, doi. 10.1038/ng.216
    By:
    • Kong, Augustine;
    • Masson, Gisli;
    • Frigge, Michael L.;
    • Gylfason, Arnaldur;
    • Zusmanovich, Pasha;
    • Thorleifsson, Gudmar;
    • Olason, Pall I.;
    • Ingason, Andres;
    • Steinberg, Stacy;
    • Rafnar, Thorunn;
    • Sulem, Patrick;
    • Mouy, Magali;
    • Jonsson, Frosti;
    • Thorsteinsdottir, Unmur;
    • Gudbjartsson, Daniel F.;
    • Stefansson, Hreinn;
    • Stefansson, Kari
    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 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

  • Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002746
    By:
    • Rui Li;
    • Brockschmidt, Felix F.;
    • Kiefer, Amy K.;
    • Stefansson, Hreinn;
    • Nyholt, Dale R.;
    • Song, Kijoung;
    • Vermeulen, Sita H.;
    • Kanoni, Stavroula;
    • Glass, Daniel;
    • Medland, Sarah E.;
    • Dimitriou, Maria;
    • Waterworth, Dawn;
    • Tung, Joyce Y.;
    • Geller, Frank;
    • Heilmann, Stefanie;
    • Hillmer, Axel M.;
    • Bataille, Veronique;
    • Eigelshoven, Sibylle;
    • Hanneken, Sandra;
    • Moebus, Susanne
    Publication type:
    Article

  • The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland.

    Published in:
    PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000505
    By:
    • Price, Alkes L.;
    • Helgason, Agnar;
    • Palsson, Snaebjorn;
    • Stefansson, Hreinn;
    • St. Clair, David;
    • Andreassen, Ole A.;
    • Reich, David;
    • Kong, Augustine;
    • Stefansson, Kari
    Publication type:
    Article

  • Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2024, v. 195, n. 4, p. 1, doi. 10.1002/ajmg.b.32967
    By:
    • Patel, Kejal H. S.;
    • Walters, G. Bragi;
    • Stefánsson, Hreinn;
    • Stefánsson, Kári;
    • Degenhardt, Franziska;
    • Nothen, Markus;
    • Van Der Veen, Tracey;
    • Demontis, Ditte;
    • Borglum, Anders;
    • Kristiansen, Mark;
    • Bass, Nicholas J.;
    • McQuillin, Andrew
    Publication type:
    Article

  • TCF4 (e2-2; ITF2): A Schizophrenia-Associated Gene With Pleiotropic Effects on Human Disease.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 1, p. 1, doi. 10.1002/ajmg.b.32109
    By:
    • Navarrete, Katherinne;
    • Pedroso, Inti;
    • De Jong, Simone;
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Stefansson, Kari;
    • Ophoff, Roel A.;
    • Schalkwyk, Leonard C.;
    • Collier, David A.
    Publication type:
    Article

  • 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

  • Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction.

    Published in:
    2018
    By:
    • Reginsson, Gunnar W.;
    • Ingason, Andres;
    • Euesden, Jack;
    • Bjornsdottir, Gyda;
    • Olafsson, Sigurgeir;
    • Sigurdsson, Engilbert;
    • Oskarsson, Hogni;
    • Tyrfingsson, Thorarinn;
    • Runarsdottir, Valgerdur;
    • Hansdottir, Ingunn;
    • Steinberg, Stacy;
    • Stefansson, Hreinn;
    • Gudbjartsson, Daniel F.;
    • Thorgeirsson, Thorgeir E.;
    • Stefansson, Kari
    Publication type:
    journal article

  • CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD.

    Published in:
    2006
    By:
    • Magnusson, Kristinn P.;
    • Duan, Shan;
    • Sigurdsson, Haraldur;
    • Petursson, Hjorvar;
    • Zhenglin Yang;
    • Yu Zhao;
    • Bernstein, Paul S.;
    • Ge, Jian;
    • Jonasson, Fridbert;
    • Stefansson, Einar;
    • Helgadottir, Gudleif;
    • Zabriskie, Norman A.;
    • Jonsson, Thorlakur;
    • Björnsson, Asgeir;
    • Thorlacius, Theodora;
    • Jonsson, Palmi V.;
    • Thorleifsson, Gudmar;
    • Kong, Augustine;
    • Stefansson, Hreinn;
    • Kang Zhang
    Publication type:
    journal article

  • CNVs conferring risk of autism or schizophrenia affect cognition in controls.

    Published in:
    Nature, 2014, v. 505, n. 7483, p. 361, doi. 10.1038/nature12818
    By:
    • Stefansson, Hreinn;
    • Meyer-Lindenberg, Andreas;
    • Steinberg, Stacy;
    • Magnusdottir, Brynja;
    • Morgen, Katrin;
    • Arnarsdottir, Sunna;
    • Bjornsdottir, Gyda;
    • Walters, G. Bragi;
    • Jonsdottir, Gudrun A.;
    • Doyle, Orla M.;
    • Tost, Heike;
    • Grimm, Oliver;
    • Kristjansdottir, Solveig;
    • Snorrason, Heimir;
    • Davidsdottir, Solveig R.;
    • Gudmundsson, Larus J.;
    • Jonsson, Gudbjorn F.;
    • Stefansdottir, Berglind;
    • Helgadottir, Isafold;
    • Haraldsson, Magnus
    Publication type:
    Article

  • Early treatment response as predictor of long-term outcome in a clinical cohort of children with ADHD.

    Published in:
    European Child & Adolescent Psychiatry, 2024, v. 33, n. 2, p. 357, doi. 10.1007/s00787-023-02158-z
    By:
    • Houmann, Tine Bodil;
    • Kaalund-Brok, Kristine;
    • Clemmensen, Lars;
    • Petersen, Morten Aagaard;
    • Plessen, Kerstin Jessica;
    • Bilenberg, Niels;
    • Verhulst, Frank;
    • Jeppesen, Pia;
    • Rasmussen, Henrik Berg;
    • Bjerre, Ditte;
    • Madsen, Majbritt Busk;
    • Ferrero, Laura;
    • Linnet, Kristian;
    • Thomsen, Ragnar;
    • Jürgens, Gesche;
    • Stage, Claus;
    • Stefansson, Hreinn;
    • Hankemeier, Thomas;
    • Kaddurah-Daouk, Rima;
    • Brunak, Søren
    Publication type:
    Article

  • The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia.

    Published in:
    Journal of Clinical Investigation, 2015, v. 125, n. 9, p. 3714, doi. 10.1172/JCI82636
    By:
    • Doyle, Orla M.;
    • Bois, Catherine;
    • Thomson, Pippa;
    • Romaniuk, Liana;
    • Whitcher, Brandon;
    • Williams, Steven C. R.;
    • Turkheimer, Federico E.;
    • Stefansson, Hreinn;
    • McIntosh, Andrew M.;
    • Mehta, Mitul A.;
    • Lawrie, Stephen M.
    Publication type:
    Article

  • Predicting the probability of death using proteomics.

    Published in:
    Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02289-6
    By:
    • Eiriksdottir, Thjodbjorg;
    • Ardal, Steinthor;
    • Jonsson, Benedikt A.;
    • Lund, Sigrun H.;
    • Ivarsdottir, Erna V.;
    • Norland, Kristjan;
    • Ferkingstad, Egil;
    • Stefansson, Hreinn;
    • Jonsdottir, Ingileif;
    • Holm, Hilma;
    • Rafnar, Thorunn;
    • Saemundsdottir, Jona;
    • Norddahl, Gudmundur L.;
    • Thorgeirsson, Gudmundur;
    • Gudbjartsson, Daniel F.;
    • Sulem, Patrick;
    • Thorsteinsdottir, Unnur;
    • Stefansson, Kari;
    • Ulfarsson, Magnus O.
    Publication type:
    Article

  • Neuregulin1 (NRG1) Signaling through Fyn Modulates NMDA Receptor Phosphorylation: Differential Synaptic Function in NRG1<sup>+/-</sup> Knock-Outs Compared with Wild-Type Mice.

    Published in:
    Journal of Neuroscience, 2007, v. 27, n. 17, p. 4519, doi. 10.1523/JNEUROSCI.4314-06.2007
    By:
    • Bjarnadottir, Maria;
    • Misner, Dinah L.;
    • Haverfield-Gross, Sascha;
    • Bruun, Silas;
    • Helgason, Vignir G.;
    • Stefansson, Hreinn;
    • Sigmundsson, Arnar;
    • Firth, David R.;
    • Nielsen, Berit;
    • Stefansdottir, Ragnheidur;
    • Novak, Thomas J.;
    • Stefansson, Kari;
    • Gurney, Mark E.;
    • Andresson, Thorkell
    Publication type:
    Article

  • Data Resource Profile: The Copenhagen Hospital Biobank (CHB).

    Published in:
    2021
    By:
    • Sørensen, Erik;
    • Christiansen, Lene;
    • Wilkowski, Bartlomiej;
    • Larsen, Margit H;
    • Burgdorf, Kristoffer S;
    • Thørner, Lise W;
    • Nissen, Janna;
    • Pedersen, Ole B;
    • Banasik, Karina;
    • Brunak, Søren;
    • Bundgaard, Henning;
    • Stefánsson, Hreinn;
    • Stefánsson, Kari;
    • Melbye, Mads;
    • Ullum, Henrik
    Publication type:
    journal article

  • A genome‐wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 1, p. 102, doi. 10.1002/epi4.12297
    By:
    • Berghuis, Bianca;
    • Stapleton, Caragh;
    • Sonsma, Anja C. M.;
    • Hulst, Janic;
    • Haan, Gerrit‐Jan;
    • Lindhout, Dick;
    • Demurtas, Rita;
    • Krause, Roland;
    • Depondt, Chantal;
    • Kunz, Wolfram S.;
    • Zara, Federico;
    • Striano, Pasquale;
    • Craig, John;
    • Auce, Pauls;
    • Marson, Anthony G.;
    • Stefansson, Hreinn;
    • O'Brien, Terence J.;
    • Johnson, Michael R.;
    • Sills, Graeme J.;
    • Wolking, Stefan
    Publication type:
    Article

  • Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 19, p. 5637, doi. 10.1093/hmg/ddv277
    By:
    • Huttenlocher, Johanna;
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Helgadottir, Hafdis T.;
    • Sveinbjörnsdóttir, Sigurlaug;
    • Riess, Olaf;
    • Bauer, Peter;
    • Stefansson, Kari
    Publication type:
    Article

  • Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

    Published in:
    Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1156362
    By:
    • Boothman, Isabelle;
    • Clayton, Lisa M.;
    • McCormack, Mark;
    • McKibben Driscoll, Alexandra;
    • Stevelink, Remi;
    • Moloney, Patrick;
    • Krause, Roland;
    • Kunz, Wolfram S.;
    • Diehl, Sarah;
    • O'Brien, Terence J.;
    • Sills, Graeme J.;
    • de Haan, Gerrit-Jan;
    • Zara, Federico;
    • Koeleman, Bobby P.;
    • Depondt, Chantal;
    • Marson, Anthony G.;
    • Stefansson, Hreinn;
    • Stefansson, Kari;
    • Craig, John;
    • Johnson, Michael R.
    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