Search Results

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency

by Runolfsdottir, Hrafnhildur L., Sayer, John A., Indridason, Olafur S., Edvardsson, Vidar O., Jensson, Brynjar O., Arnadottir, Gudny A., Gudjonsson, Sigurjon A., Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur
Published in European Journal of Human Genetics (2021)

Abstract 4405: Sequence Variant for Atrial Fibrillation on Chromosome 4q25 near the PITX2 Gene Increases Risk for Recurrent AF

by Gulcher, Jeffrey, Holm, Hilma, Gudbjartsson, Daniel, Arnar, David, Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Circulation (2008)

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)

Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial

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, Hardarson, Thordur, Kristinsson, Arni, Topol, Eric J, Gulcher, Jeffrey, Kong, Augustine, Gurney, Mark, Thorgeirsson, Gudmundur, Stefansson, Kari
Published in JAMA (2009)

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)

The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in Iceland.

by Styrkarsdottir, Unnur, Lund, Sigrun H, Saevarsdottir, Saedis, Magnusson, Magnus I, Gunnarsdottir, Kristbjorg, Norddahl, Gudmundur L, Frigge, Michael L, Ivarsdottir, Erna V, Bjornsdottir, Gyda, Holm, Hilma, Thorgeirsson, Gudmundur, Rafnar, Thorunn, Jonsdottir, Ingileif, Ingvarsson, Thorvaldur, Jonsson, Helgi, Sulem, Patrick, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Stefansson, Kari
Published in Arthritis & Rheumatology (2022)

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)

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency.

by Runolfsdottir, Hrafnhildur L, Sayer, John A, Indridason, Olafur S, Edvardsson, Vidar O, Jensson, Brynjar O, Arnadottir, Gudny A, Gudjonsson, Sigurjon A, Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur
Published in European Journal of Human Genetics (2021)

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)

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

by Björnsson, Þorsteinn, Þórólfsdóttir, Rósa B., Sveinbjornsson, Gardar, sulem, patrick, Norðdahl, Guðmundur L., Helgadóttir, Anna, Grétarsdóttir, Sólveig, Magnusdóttir, Auður, Danielsen, Ragnar, Sigurðsson, Emil Lárus, Adalsteinsdottir, Berglind, Gunnarsson, Sverrir I, Jonsdottir, Ingileif, Arnar, Davíð O., Helgason, Hróðmar, Gudbjartsson, Tomas, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Holm, Hilma, Stefansson, Kari
Published in European Heart Journal (2018)

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.

by Gudmundsson, Julius, Sulem, Patrick, Rafnar, Thorunn, Bergthorsson, Jon T, Manolescu, Andrei, Gudbjartsson, Daniel, Agnarsson, Bjarni A, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Blondal, Thorarinn, Jakobsdottir, Margret, Stacey, Simon N, Kostic, Jelena, Kristinsson, Kari T, Birgisdottir, Birgitta, Ghosh, Shyamali, Magnusdottir, Droplaug N, Thorlacius, Steinunn, Thorleifsson, Gudmar, Zheng, S Lilly, Sun, Jielin, Chang, Bao-Li, Elmore, J Bradford, Breyer, Joan P, McReynolds, Kate M, Bradley, Kevin M, Yaspan, Brian L, Wiklund, Fredrik, Stattin, Par, Lindström, Sara, Adami, Hans-Olov, McDonnell, Shannon K, Schaid, Daniel J, Cunningham, Julie M, Wang, Liang, Cerhan, James R, St Sauver, Jennifer L, Isaacs, Sara D, Wiley, Kathleen E, Partin, Alan W, Walsh, Patrick C, Polo, Sonia, Ruiz-Echarri, Manuel, Navarrete, Sebastian, Fuertes, Fernando, Saez, Berta, Godino, Javier, Weijerman, Philip C, Swinkels, Dorine W, Aben, Katja K
Published in Nature Genetics (2009)

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

by Kiemeney, Lambertus A, Thorlacius, Steinunn, Sulem, Patrick, Geller, Frank, Aben, Katja K. H, 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 2008

The CRTAC1 protein in plasma associates with osteoarthritis and predicts progression to joint replacements : A Large-Scale Proteomics Scan in Iceland

by Styrkarsdottir, Unnur, Lund, Sigrun H., Sævarsdóttir, Sædís, Magnusson, Magnus I., Gunnarsdottir, Kristbjorg, Norddahl, Gudmundur L., Frigge, Michael L., Ivarsdottir, Erna V., Bjornsdottir, Gyda, Holm, Hilma, Thorgeirsson, Gudmundur, Rafnar, Thorunn, Jónsdóttir, Ingileif, Ingvarsson, Þorvaldur, Jónsson, Helgi, Sulem, Patrick, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Stefansson, Kari
Published in Arthritis & Rheumatology (2021)

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

by Kiemeney, Lambertus A, Thorlacius, Steinunn, Sulem, Patrick, Geller, Frank, Aben, Katja K H, 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
Published in Nature Genetics (2008)

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

by Ferkingstad, Egil, Oddsson, Asmundur, Gretarsdottir, Solveig, Benonisdottir, Stefania, Thorleifsson, Gudmar, Deaton, Aimee M., Jónsson, Stefán, Stefánsson, Ólafur A., Norðdahl, Guðmundur L., Zink, Florian, Arnadottir, Gudny, Gunnarsson, Bjarni, Halldorsson, Gisli, Helgadottir, Anna, Jensson, Brynjar Örn, Kristjánsson, Ragnar P., Sveinbjornsson, Gardar, Sverrisson, Davíð A., Másson, Gísli, Olafsson, Isleifur, Eyjólfsson, Guðmundur I., Sigurðardóttir, Ólöf, Holm, Hilma, Jonsdottir, Ingileif, Ólafsson, Sigurður, Steingrimsdottir, Thora, Rafnar, Thorunn, Björnsson, Einar Stefán, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, sulem, patrick, Stefansson, Kari
Published in Nature Communications (2018)

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, Søren, 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, Malekzadeh, Mahyar, van den Berg, Leonard H, Ophoff, Roel A, Veldink, Jan H, Zeegers, Maurice P, Kellen, Eliane, Fostinelli, Jacopo, Andreoli, Daniele, Arici, Cecilia, Porru, Stefano, Buntinx, Frank, Ghaderi, Abbas, Golka, Klaus, Mayordomo, José I, Matullo, Giuseppe, Kumar, Rajiv, Steineck, Gunnar, Kiltie, Anne E, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari, Kiemeney, Lambertus A
Published in Human Molecular Genetics (2011)

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

by Gudmundsson, Julius, Sigurðsson, Jón K., Stefánsdóttir, Lilja, Agnarsson, Bjarni A., Ísaksson, Helgi J., Stefánsson, Ólafur A., Guðjónsson, Sigurjón Axel, Gudbjartsson, Daniel, Másson, Gísli, Frigge, Michael L., Stacey, Simon N., sulem, patrick, Halldorsson, Gisli, Tragante, Vinicius, Holm, Hilma, Eyjólfsson, Guðmundur I., Sigurðardóttir, Ólöf, Olafsson, Isleifur, Jónsson, Þorvaldur, Jónsson, Eirikur, Barkardottir, Rosa Bjork, Hilmarsson, Rafn, Asselbergs, Folkert W., Geirsson, Guðmundur, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, Stefansson, Kari
Published in Nature Communications (2018)

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

by Óskarsson, Guðjón R., Oddsson, Asmundur, Magnusson, Magnus Karl, Kristjansson, Ragnar, Halldorsson, Gisli, Ferkingstad, Egil, Zink, Florian, Helgadottir, Anna, Ívarsdóttir, Erna V., Arnadottir, Gudny, Jensson, Brynjar Örn, Katrinardottir, Hildigunnur, Sveinbjornsson, Gardar, Kristinsdóttir, Anna Margrét, Lee, Amy L., Sæmundsdóttir, Jóna, Stefánsdóttir, Lilja, Sigurðsson, Jón K., Davíðsson, Ólafur B., Benonisdottir, Stefania, Jónasdóttir, Áslaug, Jónasdóttir, Aðalbjörg, Jonsson, Stefan, Guðmundsson, Reynir L., Asselbergs, Folkert W., Tragante, Vinicius, Gunnarsson, Bjarni, Másson, Gísli, Thorleifsson, Gudmar, Rafnar, Thorunn, Holm, Hilma, Olafsson, Isleifur, Önundarson, Páll Torfi, Gudbjartsson, Daniel, Norðdahl, Guðmundur L., Thorsteinsdottir, Unnur, sulem, patrick, Stefansson, Kari
Published in Communications Biology (2020)

A common variant associated with prostate cancer in European and African populations

by Amundadottir, Laufey T, Sulem, Patrick, Gudmundsson, Julius, Helgason, Agnar, Baker, Adam, Agnarsson, Bjarni A, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Cazier, Jean-Baptiste, Sainz, Jesus, Jakobsdottir, Margret, Kostic, Jelena, Magnusdottir, Droplaug N, Ghosh, Shyamali, Agnarsson, Kari, Birgisdottir, Birgitta, Le Roux, Louise, Olafsdottir, Adalheidur, Blondal, Thorarinn, Andresdottir, Margret, Gretarsdottir, Olafia Svandis, Bergthorsson, Jon T, Gudbjartsson, Daniel, Gylfason, Arnaldur, Thorleifsson, Gudmar, Manolescu, Andrei, Kristjansson, Kristleifur, Geirsson, Gudmundur, Isaksson, Helgi, Douglas, Julie, Johansson, Jan-Erik, Bälter, Katarina, Wiklund, Fredrik, Montie, James E, Yu, Xiaoying, Suarez, Brian K, Ober, Carole, Cooney, Kathleen A, Gronberg, Henrik, Catalona, William J, Einarsson, Gudmundur V, Barkardottir, Rosa B, Gulcher, Jeffrey R, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2006)