Search Results

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

by Helgadottir, Anna, Manolescu, Andrei, Helgason, Agnar, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Gretarsdottir, Solveig, Magnusson, Kristinn P, Gudmundsson, Gudmundur, Hicks, Andrew, Jonsson, Thorlakur, Grant, Struan F A, Sainz, Jesus, O'Brien, Stephen J, Sveinbjornsdottir, Sigurlaug, Valdimarsson, Einar M, Matthiasson, Stefan E, Levey, Allan I, Abramson, Jerome L, Reilly, Murdach P, Vaccarino, Viola, Wolfe, Megan L, Gudnason, Vilmundur, Quyyumi, Arshed A, Topol, Eric J, Rader, Daniel J, Thorgeirsson, Gudmundur, Gulcher, Jeffrey R, Hakonarson, Hakon, Kong, Augustine, Stefansson, Kari
Published in Nature Genetics (2007)

Discovery of common variants associated with low TSH levels and thyroid cancer risk.

by Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Jonasson, Jon G, Masson, Gisli, He, Huiling, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Stacey, Simon N, Johannsdottir, Hrefna, Helgadottir, Hafdis Th, Li, Wei, Nagy, Rebecca, Ringel, Matthew D, Kloos, Richard T, de Visser, Marieke C H, Plantinga, Theo S, den Heijer, Martin, Aguillo, Esperanza, Panadero, Angeles, Prats, Enrique, Garcia-Castaño, Almudena, De Juan, Ana, Rivera, Fernando, Walters, G Bragi, Bjarnason, Hjordis, Tryggvadottir, Laufey, Eyjolfsson, Gudmundur I, Bjornsdottir, Unnur S, Holm, Hilma, Olafsson, Isleifur, Kristjansson, Kristleifur, Kristvinsson, Hoskuldur, Magnusson, Olafur T, Thorleifsson, Gudmar, Gulcher, Jeffrey R, Kong, Augustine, Kiemeney, Lambertus A L M, Jonsson, Thorvaldur, Hjartarson, Hannes, Mayordomo, Jose I, Netea-Maier, Romana T, de la Chapelle, Albert, Hrafnkelsson, Jon, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Published in Nature Genetics (2013)

Physical and neuro-behavioural determinants of reproductive onset and success

by Day, Felix R., Helgason, Hannes, Chasman, Daniel I., Rose, Lynda M., Loh, Po-Ru, Scott, Robert A., Helgason, Agnar, Kong, Augustine, Masson, Gisli, Magnusson, Olafur Th., Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Buring, Julie E., Ridker, Paul M., Sulem, Patrick, Stefansson, Kari, Ong, Ken K., Perry, John R.B.
Published in Nature Genetics (2016)

Parental origin of sequence variants associated with complex diseases

by Kong, Augustine, Steinthorsdottir, Valgerdur, Masson, Gisli, Thorleifsson, Gudmar, Sulem, Patrick, Besenbacher, Søren, 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, Benediktsson, Rafn, Olafsson, Jon H, Johannsson, Oskar Th, Hreidarsson, Astradur B, Sigurdsson, Gunnar, Ferguson-Smith, Anne C, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Stefansson, Kari, Lauritzen, Torsten
Published in Nature (2009)

Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland

by Thorgeirsson, Thorgeir E., Oskarsson, Högni, Desnica, Natasa, Kostic, Jelena Pop, Stefansson, Jon G., Kolbeinsson, Halldor, Lindal, Eirikur, Gagunashvili, Nikolai, Frigge, Michael L., Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R.
Published 2003

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)

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)

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

by Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Blondal, Thorarinn, Gylfason, Arnaldur, Agnarsson, Bjarni A, Benediktsdottir, Kristrun R, Magnusdottir, Droplaug N, Orlygsdottir, Gudbjorg, Jakobsdottir, Margret, Stacey, Simon N, Sigurdsson, Asgeir, Wahlfors, Tiina, Tammela, Teuvo, Breyer, Joan P, McReynolds, Kate M, Bradley, Kevin M, Saez, Berta, Godino, Javier, Navarrete, Sebastian, Fuertes, Fernando, Murillo, Laura, Polo, Eduardo, Aben, Katja K, van Oort, Inge M, Suarez, Brian K, Helfand, Brian T, Kan, Donghui, Zanon, Carlo, Frigge, Michael L, Kristjansson, Kristleifur, Gulcher, Jeffrey R, Einarsson, Gudmundur V, Jonsson, Eirikur, Catalona, William J, Mayordomo, Jose I, Kiemeney, Lambertus A, Smith, Jeffrey R, Schleutker, Johanna, Barkardottir, Rosa B, Kong, Augustine, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Published in Nature Genetics (2009)

Several common variants modulate heart rate, PR interval and QRS duration

by Holm, Hilma, Gudbjartsson, Daniel F, Arnar, David O, Thorleifsson, Gudmar, Thorgeirsson, Gudmundur, Stefansdottir, Hrafnhildur, Gudjonsson, Sigurjon A, Jonasdottir, Aslaug, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Løchen, Maja-Lisa, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

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

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, Pedersen, Jesper H, Pack, Allan I, de Visser, Marieke C H, Kiemeney, Lambertus A, Geirsson, Arni J, Eyjolfsson, Gudmundur I, Olafsson, Isleifur, Kong, Augustine, Masson, Gisli, Jonsson, Helgi, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Stefansson, Kari
Published in Nature Genetics (2012)

A common variant at 8q24.21 is associated with renal cell cancer.

by Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Masson, Gisli, Petursdottir, Vigdis, Hardarson, Sverrir, Gudjonsson, Sigurjon A, Johannsdottir, Hrefna, Helgadottir, Hafdis Th, Stacey, Simon N, Magnusson, Olafur Th, Helgason, Hannes, Panadero, Angeles, van der Zanden, Loes F, Aben, Katja K H, Vermeulen, Sita H, Oosterwijk, Egbert, Kong, Augustine, Mayordomo, Jose I, Sverrisdottir, Asgerdur, Jonsson, Eirikur, Gudbjartsson, Tomas, Einarsson, Gudmundur V, Kiemeney, Lambertus A, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Published in Nature Communications (2014)

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.

by Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Helgadottir, Hafdis T, Bomer, Nils, Metrustry, Sarah, Bierma-Zeinstra, S, Strijbosch, Annelieke M, Evangelou, Evangelos, Hart, Deborah, Beekman, Marian, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Eiriksson, Finnur F, Thorsteinsdottir, Margret, Frigge, Michael L, Kong, Augustine, Gudjonsson, Sigurjon A, Magnusson, Olafur T, Masson, Gisli, Hofman, Albert, Arden, Nigel K, Ingvarsson, Thorvaldur, Lohmander, Stefan, Kloppenburg, Margreet, Rivadeneira, Fernando, Nelissen, Rob G H H, Spector, Tim, Uitterlinden, Andre, Slagboom, P Eline, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Valdes, Ana M, Meulenbelt, Ingrid, van Meurs, Joyce, Jonsson, Helgi, Stefansson, Kari
Published in Nature Genetics (2014)

Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population

by Stefansson, Hreinn, Sarginson, Jane, Kong, Augustine, Yates, Phil, Steinthorsdottir, Valgerdur, Gudfinnsson, Einar, Gunnarsdottir, Steinunn, Walker, Nicholas, Petursson, Hannes, Crombie, Caroline, Ingason, Andres, Gulcher, Jeffrey R., Stefansson, Kari, Clair, David St
Published 2003

Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.

by Grarup, Niels, Sulem, Patrick, Sandholt, Camilla, Thorleifsson, Gudmar, Ahluwalia, Tarunveer, Steinthorsdottir, Valgerdur, Bjarnason, Helgi, Gudbjartsson, Daniel, Magnusson, Olafur, Sparsø, Thomas, Albrechtsen, Anders, Kong, Augustine, Masson, Gisli, Tian, Geng, Cao, Hongzhi, Nie, Chao, Kristiansen, Karsten, Husemoen, Lise, Thuesen, Betina, Li, Yingrui, Nielsen, Rasmus, Linneberg, Allan, Olafsson, Isleifur, Eyjolfsson, Gudmundur, Jørgensen, Torben, Wang, Jun, Hansen, Torben, Thorsteinsdottir, Unnur, Stefánsson, Kari, Pedersen, Oluf
Published 2013

Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases

by Gudbjartsson, Daniel F, Holm, Hilma, Indridason, Olafur S, Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C H, den Heijer, Martin, Wetzels, Jack F M, Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S, Eyjolfsson, Gudmundur I, Kiemeney, Lambertus A, Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in PLoS Genetics (2011)

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.

by Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Masson, Gisli, Agnarsson, Bjarni A, Benediktsdottir, Kristrun R, Sigurdsson, Asgeir, Magnusson, Olafur Th, Gudjonsson, Sigurjon A, Magnusdottir, Droplaug N, Johannsdottir, Hrefna, Helgadottir, Hafdis Th, Stacey, Simon N, Jonasdottir, Adalbjorg, Olafsdottir, Stefania B, Thorleifsson, Gudmar, Jonasson, Jon G, Tryggvadottir, Laufey, Navarrete, Sebastian, Fuertes, Fernando, Helfand, Brian T, Hu, Qiaoyan, Csiki, Irma E, Mates, Ioan N, Jinga, Viorel, Aben, Katja K H, van Oort, Inge M, Vermeulen, Sita H, Donovan, Jenny L, Hamdy, Freddy C, Ng, Chi-Fai, Chiu, Peter K F, Lau, Kin-Mang, Ng, Maggie C Y, Gulcher, Jeffrey R, Kong, Augustine, Catalona, William J, Mayordomo, Jose I, Einarsson, Gudmundur V, Barkardottir, Rosa B, Jonsson, Eirikur, Mates, Dana, Neal, David E, Kiemeney, Lambertus A, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Published in Nature Genetics (2013)

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

by Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, 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, Zhang, Kang, Stefansson, Kari, Gulcher, Jeffrey R
Published in PLoS Medicine (2009)

Genetic correction of PSA values using sequence variants associated with PSA levels

by Gudmundsson, Julius, Besenbacher, Soren, Sulem, Patrick, Gudbjartsson, Daniel F., Olafsson, Isleifur, Arinbjarnarson, Sturla, Agnarsson, Bjarni A., Benediktsdottir, Kristrun R., Isaksson, Helgi J., Kostic, Jelena P., Gudjonsson, Sigurjon A., Stacey, Simon N., Gylfason, Arnaldur, Sigurdsson, Asgeir, Holm, Hilma, Bjornsdottir, Unnur S., Eyjolfsson, Gudmundur I., Navarrete, Sebastian, Fuertes, Fernando, Garcia-Prats, Maria D., Polo, Eduardo, Checherita, Ionel A., Jinga, Mariana, Badea, Paula, Aben, Katja K., Schalken, Jack A., van Oort, Inge M., Sweep, Fred C., Helfand, Brian T., Davis, Michael, Donovan, Jenny L., Hamdy, Freddie C., Kristjansson, Kristleifur, Gulcher, Jeffrey R., Masson, Gisli, Kong, Augustine, Catalona, William J., Mayordomo, Jose I., Geirsson, Gudmundur, Einarsson, Gudmundur V., Barkardottir, Rosa B., Jonsson, Eirikur, Jinga, Viorel, Mates, Dana, Kiemeney, Lambertus A., Neal, David E., Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Published in Science Translational Medicine (2010)

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk

by Rafnar, Thorunn, Sulem, Patrick, Besenbacher, Soren, Gudbjartsson, Daniel F., Zanon, Carlo, Gudmundsson, Julius, Stacey, Simon N., Kostic, Jelena P., Thorgeirsson, Thorgeir E., Thorleifsson, Gudmar, Bjarnason, Hjordis, Skuladottir, Halla, Gudbjartsson, Tomas, Isaksson, Helgi J., Isla, Dolores, Murillo, Laura, García-Prats, Maria D., Panadero, Angeles, Aben, Katja K.H., Vermeulen, Sita H., van der Heijden, Henricus F.M., Feser, William, Miller, York E., Bunn, Paul A., Kong, Augustine, Wolf, Holly J., Franklin, Wilbur A., Mayordomo, Jose I, Kiemeney, Lambertus A., Jonsson, Steinn, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Cancer Research (2011)

Neuregulin 1 and susceptibility to schizophrenia

by Stefansson, Hreinn, Sigurdsson, Engilbert, Steinthorsdottir, Valgerdur, Bjornsdottir, Soley, Sigmundsson, Thordur, Ghosh, Shyamali, Brynjolfsson, Jon, Gunnarsdottir, Steinunn, Ivarsson, Omar, Chou, Thomas T, Hjaltason, Omar, Birgisdottir, Birgitta, Jonsson, Helgi, Gudnadottir, Vala G, Gudmundsdottir, Elsa, Bjornsson, Asgeir, Ingvarsson, Brynjolfur, Ingason, Andres, Sigfusson, Sigmundur, Hardardottir, Hronn, Harvey, Richard P, Lai, Donna, Zhou, Mingdong, Brunner, Daniela, Mutel, Vincent, Gonzalo, Acuna, Lemke, Greg, Sainz, Jesus, Johannesson, Gardar, Andresson, Thorkell, Gudbjartsson, Daniel, Manolescu, Andrei, Frigge, Michael L, Gurney, Mark E, Kong, Augustine, Gulcher, Jeffrey R, Petursson, Hannes, Stefansson, Kari
Published in The American Journal of Human Genetics (2008)