Search Results

Weighting sequence variants based on their annotation increases power of whole-genome association studies.

by Sveinbjornsson, Gardar, Albrechtsen, Anders, Zink, Florian, Gudjonsson, Sigurjón A, Oddson, Asmundur, Másson, Gísli, Holm, Hilma, Kong, Augustine, Thorsteinsdottir, Unnur, Sulem, Patrick, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Nature Genetics (2016)

Large-scale whole-genome sequencing of the Icelandic population

by Gudbjartsson, Daniel F, Helgason, Hannes, Gudjonsson, Sigurjon A, Zink, Florian, Oddson, Asmundur, Gylfason, Arnaldur, Besenbacher, Soren, Magnusson, Gisli, Halldorsson, Bjarni V, Hjartarson, Eirikur, Sigurdsson, Gunnar Th, Stacey, Simon N, Frigge, Michael L, Holm, Hilma, Saemundsdottir, Jona, Helgadottir, Hafdis Th, Johannsdottir, Hrefna, Sigfusson, Gunnlaugur, Thorgeirsson, Gudmundur, Sverrisson, Jon Th, Gretarsdottir, Solveig, Walters, G Bragi, Rafnar, Thorunn, Thjodleifsson, Bjarni, Bjornsson, Einar S, Olafsson, Sigurdur, Thorarinsdottir, Hildur, Steingrimsdottir, Thora, Gudmundsdottir, Thora S, Theodors, Asgeir, Jonasson, Jon G, Sigurdsson, Asgeir, Bjornsdottir, Gyda, Jonsson, Jon J, Thorarensen, Olafur, Ludvigsson, Petur, Gudbjartsson, Hakon, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Arnar, David O, Magnusson, Olafur Th, Kong, Augustine, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Sulem, Patrick, Stefansson, Kari
Published in Nature Genetics (2015)

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)

Large-scale whole-genome sequencing of the Icelandic population.

by Gudbjartsson, Daniel F, Helgason, Hannes, Gudjonsson, Sigurjon A, Zink, Florian, Oddson, Asmundur, Gylfason, Arnaldur, Besenbacher, Soren, Magnusson, Gisli, Halldorsson, Bjarni V, Hjartarson, Eirikur, Sigurdsson, Gunnar Th, Stacey, Simon N, Frigge, Michael L, Holm, Hilma, Saemundsdottir, Jona, Helgadottir, Hafdis Th, Johannsdottir, Hrefna, Sigfusson, Gunnlaugur, Thorgeirsson, Gudmundur, Sverrisson, Jon Th, Gretarsdottir, Solveig, Walters, G Bragi, Rafnar, Thorunn, Thjodleifsson, Bjarni, Bjornsson, Einar S, Olafsson, Sigurdur, Thorarinsdottir, Hildur, Steingrimsdottir, Thora, Gudmundsdottir, Thora S, Theodors, Asgeir, Jonasson, Jon G, Sigurdsson, Asgeir, Bjornsdottir, Gyda, Jonsson, Jon J, Thorarensen, Olafur, Ludvigsson, Petur, Gudbjartsson, Hakon, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Arnar, David O, Magnusson, Olafur Th, Kong, Augustine, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Sulem, Patrick, Stefansson, Kari
Published in Nature Genetics (2015)

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 J, 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)

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

by Thorleifsson, Gudmar, Magnusson, Kristinn P, Sulem, Patrick, Walters, G Bragi, Gudbjartsson, Daniel F, Stefansson, Hreinn, Jonsson, Thorlakur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Stefansdottir, Gerdur, Masson, Gisli, Hardarson, Gudmundur A, Petursson, Hjorvar, Arnarsson, Arsaell, Motallebipour, Mehdi, Wallerman, Ola, Wadelius, Claes, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Jonasson, Fridbert, Stefansson, Kari
Published in Science (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)

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)

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)

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)

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)

Parental origin of sequence variants associated with complex diseases

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, Benediktsson, Rafn, Olafsson, Jon H, Johannsson, Oskar Th, Hreidarsson, Astradur B, Sigurdsson, Gunnar, Ferguson-Smith, Anne C, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature (2011)

Rate of de novo mutations and the importance of father's age to disease risk.

by Kong, Augustine, Frigge, Michael L, Masson, Gisli, Besenbacher, Soren, Sulem, Patrick, Magnusson, Gisli, Gudjonsson, Sigurjon A, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Wong, Wendy S W, Sigurdsson, Gunnar, Walters, G Bragi, Steinberg, Stacy, Helgason, Hannes, Thorleifsson, Gudmar, Gudbjartsson, Daniel F, Helgason, Agnar, Magnusson, Olafur Th, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature (2013)

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

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, Ristau, Tina, Patel, Shirrina, Liakopoulos, Sandra, van de Ven, Johannes P H, Hoyng, Carel B, Ferreyra, Henry, Duan, Yaou, Bernstein, Paul S, Geirsdottir, Asbjorg, Helgadottir, Gudleif, Stefansson, Einar, den Hollander, Anneke I, Zhang, Kang, Jonasson, Fridbert, Sigurdsson, Haraldur, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2013)

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

by Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Sulem, Patrick, Gudbjartsson, Daniel F, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Oddsson, Asmundur, Helgason, Agnar, Magnusson, Olafur T, Walters, G Bragi, Frigge, Michael L, Helgadottir, Hafdis T, Johannsdottir, Hrefna, Bergsteinsdottir, Kristin, Ogmundsdottir, Margret H, Center, Jacqueline R, Nguyen, Tuan V, Eisman, John A, Christiansen, Claus, Steingrimsson, Erikur, Jonasson, Jon G, Tryggvadottir, Laufey, Eyjolfsson, Gudmundur I, Theodors, Asgeir, Jonsson, Thorvaldur, Ingvarsson, Thorvaldur, Olafsson, Isleifur, Rafnar, Thorunn, Kong, Augustine, Sigurdsson, Gunnar, Masson, Gisli, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature (2014)

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

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, Hansen, Torben, Daneshpour, Maryam S, Fallah, Mohammad-Sadegh, Hreidarsson, Astradur B, Sigurdsson, Gunnar, Azizi, Fereidoun, Benediktsson, Rafn, Masson, Gisli, Helgason, Agnar, Kong, Augustine, Gudbjartsson, Daniel F, Pedersen, Oluf, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2014)

Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets

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, Nielsen, Rasmus, Linneberg, Allan, Olafsson, Isleifur, Eyjolfsson, Gudmundur I, Jørgensen, Torben, Wang, Jun, Hansen, Torben, Thorsteinsdottir, Unnur, Stefánsson, Kari, Pedersen, Oluf
Published 2013

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

by Gudbjartsson, Daniel F, 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, Wheatley, Amanda, Altmuller, Janine, Shin, Hyoung Doo, Uh, Soo-Taek, Cheong, Hyun Sub, Jonsdottir, Brynja, Gislason, David, Park, Choon-Sik, Rasmussen, Linda M, Porsbjerg, Celeste, Hansen, Jakob W, Backer, Vibeke, Werge, Thomas, Janson, Christer, Jönsson, Ulla-Britt, Ng, Maggie C Y, Chan, Juliana, So, Wing Yee, Ma, Ronald, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Levey, Allan I, Vaccarino, Viola, Reilly, Muredach P, Rader, Daniel J, Williams, Michael J A, van Rij, Andre M, Jones, Gregory T, Trabetti, Elisabetta, Malerba, Giovanni, Pignatti, Pier Franco, Boner, Attilio, Pescollderungg, Lydia, Girelli, Domenico, Olivieri, Oliviero, Martinelli, Nicola, Ludviksson, Bjorn R, Ludviksdottir, Dora, Eyjolfsson, Gudmundur I, Arnar, David, Thorgeirsson, Gudmundur, Deichmann, Klaus, Thompson, Philip J, Wjst, Matthias, Hall, Ian P, Postma, Dirkje S, Gislason, Thorarinn, Gulcher, Jeffrey, Kong, Augustine, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2009)