Search Results

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

by Gudbjartsson, Daniel F, Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Ng, Maggie C Y, Baum, Larry, So, Wing Yee, Wong, Ka Sing, Chan, Juliana C N, Gieger, Christian, Wichmann, H-Erich, Gschwendtner, Andreas, Dichgans, Martin, Kuhlenbäumer, Gregor, Berger, Klaus, Ringelstein, E Bernd, Bevan, Steve, Markus, Hugh S, Kostulas, Konstantinos, Hillert, Jan, Sveinbjörnsdóttir, Sigurlaug, Valdimarsson, Einar M, Løchen, Maja-Lisa, Ma, Ronald C W, Darbar, Dawood, Kong, Augustine, Arnar, David O, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2009)

Linkage of essential hypertension to chromosome 18q

by Kristjansson, Kristleifur, Manolescu, Andrei, Kristinsson, Arni, Hardarson, Thordur, Knudsen, Helga, Ingason, Sigurdur, Thorleifsson, Gudmar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefansson, Kari
Published 2008

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

by Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A., Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H., Kristjansson, Ragnar P., Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P., Melsted, Pall, Halldorsson, Bjarni V., Lund, Sigrun H., Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Published in Communications Biology (2020)

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

by Gretarsdottir, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J, Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Urbonavicius, Sigitas, Lindblad, Bengt, Gottsäter, Anders, Gaetani, Eleonora, Pola, Roberto, Wells, Philip, Rodger, Marc, Forgie, Melissa, Langlois, Nicole, Corral, Javier, Vicente, Vicente, Fontcuberta, Jordi, España, Francisco, Grarup, Niels, Jørgensen, Torben, Witte, Daniel R, Hansen, Torben, Pedersen, Oluf, Aben, Katja K, de Graaf, Jacqueline, Holewijn, Suzanne, Folkersen, Lasse, Franco-Cereceda, Anders, Eriksson, Per, Collier, David A, Stefansson, Hreinn, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, Valdimarsson, Einar M, Magnadottir, Hulda B, Sveinbjornsdottir, Sigurlaug, Olafsson, Isleifur, Magnusson, Magnus Karl, Palmason, Robert, Haraldsdottir, Vilhelmina, Andersen, Karl, Onundarson, Pall T, Thorgeirsson, Gudmundur, Kiemeney, Lambertus A, Powell, Janet T, Carey, David J, Kuivaniemi, Helena, Lindholt, Jes S., Jones, Gregory T, Kong, Augustine, Blankensteijn, Jan D, Matthiasson, Stefan E, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

by Gretarsdottir, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J
Published in Nature Genetics (2011)

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.

by Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A, Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H, Kristjansson, Ragnar P, Frigge, Michael L, Stefansdottir, Lilja, Sigurdsson, Jon K, Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P, Melsted, Pall, Halldorsson, Bjarni V, Lund, Sigrun H, Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Published in Communications Biology (2020)

Abstract 2921: Genome-wide Association Reveals Sequence Variants on 4q25 that Affect the Risk of Atrial Fibrillation and Stroke

by Gulcher, Jeffrey, Gudbjartsson, Daniel, Helgadottir, Anna, Gretarsdottir, Solveig, Arnar, David, Thorleifsson, Gudmar, Thorgeirsson, Gudmundur, Hillert, Jan, Ma, Ronald, Rosand, Jonathan, Ellinor, Patrick, Holm, Hilma, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari
Published in Circulation (2007)

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

by Zeggini, Eleftheria, Panoutsopoulou, Kalliope, Southam, Lorraine, Rayner, Nigel W., Day-Williams, Aaron G., Lopes, Margarida C., Boraska, Vesna, Esko, Tonu, Evangelou, Evangelos, Hofman, Albert, Houwing-Duistermaat, Jeanine J., Ingvarsson, Thorvaldur, Jonsdottir, Ingileif, Jonsson, Helgi, Kerkhof, Hanneke J. M., Kloppenburg, Margreet, Bos, Steffan D., Mangino, Massimo, Metrustry, Sarah, Slagboom, P. Eline, Thorleifsson, Gudmar, Raine, Emma V. A., Ratnayake, Madhushika, Ricketts, Michelle, Beazley, Claude, Blackburn, Hannah, Bumpstead, Suzannah, Elliott, Katherine S., Hunt, Sarah E., Potter, Simon C., Shin, So-Youn, Yadav, Vijay K., Zhai, Guangju, Sherburn, Kate, Dixon, Kate, Arden, Elizabeth, Aslam, Nadim, Battley, Phillippa-Kate, Carluke, Ian, Doherty, Sally, Gordon, Andrew, Joseph, John, Keen, Richard, Koller, Nicola C., Mitchell, Sheryl, O'Neill, Fiona, Paling, Ellen, Reed, Mike R., Valdes, Ana M., Spector, Tim D.
Published in The Lancet (2012)

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.

by Nioi, Paul, Sigurdsson, Asgeir, Thorleifsson, Gudmar, Helgason, Hannes, Agustsdottir, Arna B, Norddahl, Gudmundur L, Helgadottir, Anna, Magnusdottir, Audur, Jonasdottir, Aslaug, Gretarsdottir, Solveig, Jonsdottir, Ingileif, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, Swinkels, Dorine W, Galesloot, Tessel E, Grarup, Niels, Jørgensen, Torben, Vestergaard, Henrik, Hansen, Torben, Lauritzen, Torsten, Linneberg, Allan, Friedrich, Nele, Krarup, Nikolaj T, Fenger, Mogens, Abildgaard, Ulrik, Hansen, Peter R, Galløe, Anders M, Braund, Peter S, Nelson, Christopher P, Hall, Alistair S, Williams, Michael J A, van Rij, Andre M, Jones, Gregory T, Patel, Riyaz S, Levey, Allan I, Hayek, Salim, Shah, Svati H, Reilly, Muredach, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Kiemeney, Lambertus A, Quyyumi, Arshed A, Rader, Daniel J, Kraus, William E, Samani, Nilesh J, Pedersen, Oluf, Thorgeirsson, Gudmundur, Masson, Gisli, Holm, Hilma
Published in New England Journal of Medicine (2016)

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

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, Erikstrup, Christian, Sørensen, Erik, Brunak, Søren, Banasik, Karina, Hansen, Thomas F, Nyegaard, Mette, Eyjolfssson, Gudmundur I, Sigurdardottir, Olof, Thorarinsson, Bjorn L, Matthiasson, Stefan E, Steingrimsdottir, Thora, Bjornsson, Einar S, Danielsen, Ragnar, Asselbergs, Folkert W, Arnar, David O, Ullum, Henrik, Bundgaard, Henning, Sulem, Patrick, Thorsteinsdottir, Unnur, Thorgeirsson, Gudmundur, Holm, Hilma, Gudbjartsson, Daniel F, Stefansson, Kari
Published in European Heart Journal (2020)

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

by Rafnar, Thorunn, Vermeulen, Sita H, Sulem, Patrick, Thorleifsson, Gudmar, Aben, Katja K, Witjes, J Alfred, Grotenhuis, Anne J, Verhaegh, Gerald W, Hulsbergen-van de Kaa, Christina A, Besenbacher, Soren, Gudbjartsson, Daniel, Stacey, Simon N, Gudmundsson, Julius, Johannsdottir, Hrefna, Bjarnason, Hjordis, Zanon, Carlo, Helgadottir, Hafdis, Jonasson, Jon Gunnlaugur, Tryggvadottir, Laufey, Jonsson, Eirikur, Geirsson, Gudmundur, Nikulasson, Sigfus, Petursdottir, Vigdis, Bishop, D Timothy, Chung-Sak, Sei, Choudhury, Ananya, Elliott, Faye, Barrett, Jennifer H, Knowles, Margaret A, de Verdier, Petra J, Ryk, Charlotta, Lindblom, Annika, Rudnai, Peter, Gurzau, Eugene, Koppova, Kvetoslava, Vineis, Paolo, Polidoro, Silvia, Guarrera, Simonetta, Sacerdote, Carlotta, Panadero, Angeles, Sanz-Velez, José I, Sanchez, Manuel, Valdivia, Gabriel, Garcia-Prats, Maria D, Hengstler, Jan G, Selinski, Silvia, Gerullis, Holger, Ovsiannikov, Daniel, Khezri, Abdolaziz, Aminsharifi, Alireza
Published in Human Molecular Genetics (2012)

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.

by Zeggini, Eleftheria, Panoutsopoulou, Kalliope, Southam, Lorraine, Rayner, Nigel W, Day-Williams, Aaron G, Lopes, Margarida C, Boraska, Vesna, Esko, Tonu, Evangelou, Evangelos, Hoffman, Albert, Houwing-Duistermaat, Jeanine J, Ingvarsson, Thorvaldur, Jonsdottir, Ingileif, Jonnson, Helgi, Kerkhof, Hanneke J, Kloppenburg, Margreet, Bos, Steffan D, Mangino, Massimo, Metrustry, Sarah, Slagboom, P Eline, Thorleifsson, Gudmar, Raine, Emma V A, Ratnayake, Madhushika, Ricketts, Michelle, Beazley, Claude, Blackburn, Hannah, Bumpstead, Suzannah, Elliott, Katherine S, Hunt, Sarah E, Potter, Simon C, Shin, So-Youn, Yadav, Vijay K, Zhai, Guangju, Sherburn, Kate, Dixon, Kate, Arden, Elizabeth, Aslam, Nadim, Battley, Phillippa-kate, Carluke, Ian, Doherty, Sally, Gordon, Andrew, Joseph, John, Keen, Richard, Koller, Nicola C, Mitchell, Sheryl, O'Neill, Fiona, Paling, Ellen, Reed, Mike R, Rivadeneira, Fernando, Swift, Diane
Published in The Lancet (2013)

Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

by Helgadottir, Anna, Sulem, Patrick, Thorgeirsson, Gudmundur, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Jensson, Brynjar Ö, Arnadottir, Gudny A, Olafsson, Isleifur, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari
Published in European Heart Journal (2018)

Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

by Helgadottir, Anna, sulem, patrick, Thorgeirsson, Gudmundur, Grétarsdóttir, Sólveig, Thorleifsson, Gudmar, Jensson, Brynjar Örn, Arnadottir, Gudny, Olafsson, Isleifur, Eyjólfsson, Guðmundur I., Sigurdardottir, Olof, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Holm, Hilma, Stefansson, Kari
Published in European Heart Journal (2018)

Two newly identified genetic determinants of pigmentation in Europeans.

by Sulem, Patrick, Gudbjartsson, Daniel F, Stacey, Simon N, Helgason, Agnar, Rafnar, Thorunn, Jakobsdottir, Margret, Steinberg, Stacy, Gudjonsson, Sigurjon A, Palsson, Arnar, Thorleifsson, Gudmar, Pálsson, Snaebjörn, Sigurgeirsson, Bardur, Thorisdottir, Kristin, Ragnarsson, Rafn, Benediktsdottir, Kristrun R, Aben, Katja K, Vermeulen, Sita H, Goldstein, Alisa M, Tucker, Margaret A, Kiemeney, Lambertus A, Olafsson, Jon H, Gulcher, Jeffrey, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2008)

Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland.

by Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Eiriksdottir, Berglind, Gudjonsson, Sigurjon A, Ingvarsson, Thorvaldur, Center, Jacqueline R, Nguyen, Tuan V, Eisman, John A, Christiansen, Claus, Thorsteinsdottir, Unnur, Sigurdsson, Gunnar, Stefansson, Kari
Published in Journal of Bone and Mineral Research (2016)

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

by Ólafsdóttir, Thorhildur, Thorleifsson, Gudmar, sulem, patrick, Stefánsson, Ólafur A., Medek, Helga, Olafsson, Karl, Ingþórsson, Orri, Guðmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli, Kristjansson, Ragnar, Frigge, Michael L., Stefánsdóttir, Lilja, Sigurðsson, Jón K., Oddsson, Asmundur, Sigurðsson, Ásgeir, Eggertsson, Hannes P., Melsted, Páll, Halldórsson, Bjarni, Lund, Sigrún Helga, Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante do O, Vinicius, Asselbergs, Folkert, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Jónsdóttir, Kristín, Rafnar, Thorunn, Stefansson, Kari
Published in Communications Biology (2020)

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.

by Kiemeney, Lambertus A, Thorlacius, Steinunn, Sulem, Patrick, Geller, Frank, Aben, Katja KH, Stacey, Simon N, Gudmundsson, Julius, Jakobsdottir, Margret, Bergthorsson, Jon T, Sigurdsson, Asgeir, Blondal, Thorarinn, Witjes, J Alfred, Vermeulen, Sita H, Hulsbergen-van de Kaa, Christina A, Swinkels, Dorine W, Ploeg, Martine, Cornel, Erik B, Vergunst, Henk, Thorgeirsson, Thorgeir E, Gudbjartsson, Daniel, Gudjonsson, Sigurjon A, Thorleifsson, Gudmar, Kristinsson, Kari T, Mouy, Magali, Snorradottir, Steinunn, Placidi, Donatella, Campagna, Marcello, Arici, Cecilia, Koppova, Kvetoslava, Gurzau, Eugene, Rudnai, Peter, Kellen, Eliane, Polidoro, Silvia, Guarrera, Simonetta, Sacerdote, Carlotta, Sanchez, Manuel, Saez, Berta, Valdivia, Gabriel, Ryk, Charlotta, de Verdier, Petra, Lindblom, Annika, Golka, Klaus, Bishop, D Timothy, Knowles, Margaret A, Nikulasson, Sigfus, Petursdottir, Vigdis, Jonsson, Eirikur, Geirsson, Gudmundur, Kristjansson, Baldvin, Mayordomo, Jose I, Steineck, Gunnar, Porru, Stefano, Buntinx, Frank, Zeegers, Maurice P, Fletcher, Tony, Kumar, Rajiv, Matullo, Giuseppe, Vineis, Paolo, Kiltie, Anne E, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Rafnar, Thorunn, Stefansson, Kari
Published in Nature Genetics (2008)

Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

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 Lingaas, Asselbergs, Folkert W, Roden, Dan M, Darbar, Dawood, Pedersen, Terje Rolf, Sabatine, Marc S., Willer, Cristen J., Løchen, Maja-Lisa, Halldorsson, Bjarni V, Jonsdottir, Ingileif, Hveem, Kristian, Arnar, David O, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Kari
Published in Communications Biology (2018)

Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis.

by Styrkarsdottir, Unnur, Lund, Sigrun H, Thorleifsson, Gudmar, Zink, Florian, Stefansson, Olafur A, Sigurdsson, Jon K, Juliusson, Kristinn, Bjarnadottir, Kristbjörg, Sigurbjornsdottir, Sara, Jonsson, Stefan, Norland, Kristjan, Stefansdottir, Lilja, Sigurdsson, Asgeir, Sveinbjornsson, Gardar, Oddsson, Asmundur, Bjornsdottir, Gyda, Gudmundsson, Reynir L, Halldorsson, Gisli H, Rafnar, Thorunn, Jonsdottir, Ingileif, Steingrimsson, Eirikur, Norddahl, Gudmundur L, Masson, Gisli, Sulem, Patrick, Jonsson, Helgi, Ingvarsson, Thorvaldur, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2019)