Search Results

Sequence variants associating with urinary biomarkers

by Benonisdottir, Stefania, Kristjansson, Ragnar P, Oddsson, Asmundur, Steinthorsdottir, Valgerdur, Mikaelsdottir, Evgenia, Kehr, Birte, Jensson, Brynjar O, Arnadottir, Gudny A, Sulem, Gerald, Sveinbjornsson, Gardar, Kristmundsdottir, Snaedis, Ivarsdottir, Erna V, Vogel, Lotte K, Tragante, Vinicius, Gunnarsson, Bjarni, Runolfsdottir, Hrafnhildur Linnet, Arthur, Joseph G, Deaton, Aimee M, Eyjolfsson, Gudmundur I, Davidsson, Olafur B, Asselbergs, Folkert W, Hreidarsson, Astradur B, Rafnar, Thorunn, Thorleifsson, Gudmar, Edvardsson, Vidar, Sigurdsson, Gunnar, Helgadottir, Anna, Halldorsson, Bjarni V, Masson, Gisli, Holm, Hilma, Onundarson, Pall T, Indridason, Olafur S, Benediktsson, Rafn, Palsson, Runolfur, Gudbjartsson, Daniel F, Olafsson, Isleifur, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari
Published 2019

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Published in Nature Communications (2020)

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

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, Jonsdottir, Birna, Thygesen, Johan H, Schwarz, Adam J, Didriksen, Michael, Stensbøl, Tine B, Brammer, Michael, Kapur, Shitij, Halldorsson, Jonas G, Hreidarsson, Stefan, Saemundsen, Evald, Sigurdsson, Engilbert, Stefansson, Kari
Published in Nature (2014)

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, 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)

Variant ASGR1 associated with a reduced risk of coronary artery disease

by Nioi, P., Sigurdsson, A., Thorleifsson, G., Helgason, H., Agustsdottir, A. B., Norddahl, G. L., Helgadottir, Anna, Magnusdottir, A., Jonasdottir, A., Grétarsdóttir, Sólveig, Jonsdottir, I, Steinthorsdottir, V., Rafnar, Thorunn, Swinkels, D. W., Galesloot, T. E., Grarup, N., Jørgensen, T, Vestergaard, H., Hansen, Torben, Lauritzen, T, Linneberg, A., Friedrich, Nele, Krarup, N T, Fenger, Mogens, Abildgaard, U., Hansen, Peter R, Galløe, Anders M., Braund, P. S., Nelson, Christopher P, Hall, Alistair S, Williams, Michael J A, van Rij, Andre M, Jones, Gregory T, Patel, Sanjay R, Levey, Allan I, Hayek, S., Shah, Svati H, Reilly, Marie, Eyjolfsson, G. I., Sigurdardottir, O., Olafsson, Isleifur, Kiemeney, L. A., Quyyumi, Arshed A, Rader, Daniel J, Kraus, W. E., Samani, Nilesh J, Pedersen, O., Thorgeirsson, G., Masson, G., Holm, Hilma, Gudbjartsson, D. F., Sulem, P., Thorsteinsdottir, Unnur, Stefansson, K
Published in New England Journal of Medicine (2016)

A Nationwide Study on Hypertrophic Cardiomyopathy in Iceland: Evidence of a MYBPC3 Founder Mutation.

by Adalsteinsdottir, Berglind, Teekakirikul, Polakit, Maron, Barry J, Burke, Michael A, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari, DePalma, Steven R, Mazaika, Erica, McDonough, Barbara, Danielsen, Ragnar, Seidman, Jonathan G, Seidman, Christine E, Gunnarsson, Gunnar Th
Published in Circulation (2014)

Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor status

by Olafsdottir, Elinborg J, Borg, Ake, Jensen, Maj-Britt, Gerdes, Anne-Marie, Johansson, Anna L V, Barkardottir, Rosa B, Johannsson, Oskar T, Ejlertsen, Bent, Sønderstrup, Ida Marie Heeholm, Hovig, Eivind, Lænkholm, Anne-Vibeke, Hansen, Thomas van Overeem, Olafsdottir, Gudridur H, Rossing, Maria, Jonasson, Jon G, Sigurdsson, Stefan, Loman, Niklas, Nilsson, Martin P, Narod, Steven A, Tryggvadottir, Laufey
Published in British Journal of Cancer (2020)

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

by Committee, Writing, van der Meer, Dennis, Bernard, Manon, Sachdev, Perminder S, Sando, Sigrid B, Schofield, Peter R, Schork, Andrew J, Schumann, Gunter, Shin, Jean, Shumskaya, Elena, Silva, Ana I, Sisodiya, Sanjay M, Steen, Vidar M, Blackburn, Nicholas B, Stein, Dan J, Strike, Lachlan T, Tamnes, Christian K, Teumer, Alexander, Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Úlfarsson, Magnús Ö, van 't Ent, Dennis, van den Bree, Marianne B M, Blangero, John, Vassos, Evangelos, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J, Zayats, Tetyana, Dale, Anders M, Djurovic, Srdjan, Agartz, Ingrid, Westlye, Lars T, Stefánsson, Hreinn, Boomsma, Dorret I, Stefánsson, Kári, Thompson, Paul M, Andreassen, Ole A, ENIGMA-CNV Working Group, Brodaty, Henry, Brouwer, Rachel M, Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D, Caspers, Svenja, Sønderby, Ida E, Cavalleri, Gianpiero L, Ching, Christopher R K, Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E, Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J C, Kaufmann, Tobias, de Zubicaray, Greig I, de Zwarte, Sonja M C, Delanty, Norman, den Braber, Anouk, Desrivieres, Sylvane, Di Forti, Marta, Doherty, Joanne L, Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Walters, G Bragi, Espeseth, Thomas, Fisher, Simon E, Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Glahn, David C, Grabe, Hans J, Groenewold, Nynke A, Abdellaoui, Abdel, Gústafsson, Ómar, Haavik, Jan, Haberg, Asta K, Hashimoto, Ryota, Hehir-Kwa, Jayne Y, Hibar, Derrek P, Hillegers, Manon H J, Hoffmann, Per, Holleran, Laurena, Hottenga, Jouke-Jan, Ames, David, Hulshoff Pol, Hilleke E, Ikeda, Masashi, Jacquemont, Sébastien, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Jönsson, Erik G, Kikuchi, Masataka, Knowles, Emma E M, Kwok, John B, Amunts, Katrin, Le Hellard, Stephanie, Linden, David E J, Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri J, Martin, Nicholas G, Mather, Karen A, Mathias, Samuel R, McMahon, Katie L, McRae, Allan F, Andersson, Micael, Medland, Sarah E, Moberget, Torgeir, Moreau, Clara, Morris, Derek W, Mühleisen, Thomas W, Murray, Robin M, Nordvik, Jan E, Nyberg, Lars, Olde Loohuis, Loes M, Ophoff, Roel A, Armstrong, Nicola J, Owen, Michael J, Paus, Tomas, Pausova, Zdenka, Peralta, Juan M, Pike, Bruce, Prieto, Carlos, Quinlan, Erin Burke, Reinbold, Céline S, Reis Marques, Tiago, Rucker, James J H
Published in JAMA Psychiatry (2019)

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

by Smith, Dirk, Helgason, Hannes, Sulem, Patrick, Bjornsdottir, Unnur Steina, Lim, Ai Ching, Sveinbjornsson, Gardar, Hasegawa, Haruki, Brown, Michael, Ketchem, Randal R, Gavala, Monica, Garrett, Logan, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Magnusson, Olafur T, Eyjolfsson, Gudmundur I, Olafsson, Isleifur, Onundarson, Pall Torfi, Sigurdardottir, Olof, Gislason, David, Gislason, Thorarinn, Ludviksson, Bjorn Runar, Ludviksdottir, Dora, Boezen, H Marike, Heinzmann, Andrea, Krueger, Marcus, Porsbjerg, Celeste, Ahluwalia, Tarunveer S, Waage, Johannes, Backer, Vibeke, Deichmann, Klaus A, Koppelman, Gerard H, Bønnelykke, Klaus, Bisgaard, Hans, Masson, Gisli, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Johnston, James A, Jonsdottir, Ingileif, Stefansson, Kari
Published in PLOS Genetics (2017)

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

Human papillomavirus types in cervical high-grade lesions or cancer among Nordic women - Potential for prevention

by Dovey de la Cour, Cecilie, Guleria, Sonia, Nygård, Mari, Trygvadóttir, Laufey, Sigurdsson, Kristjan, Liaw, Kai-Li, Hortlund, Maria, Lagheden, Camilla, Hansen, Bo T, Munk, Christian, Dillner, Joakim, Kjaer, Susanne K.
Published in Cancer Medicine (2019)

Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus.

by He, Bing, Osterholm, Anne-May, Hoverfält, Anna, Forsblom, Carol, Hjorleifsdottir, Eyrun Edda, Nilsson, Ann-Sofie, Parkkonen, Maikki, Pitkäniemi, Janne, Hreidarsson, Astradur, Sarti, Cinzia, McKnight, Amy Jayne, Maxwell, A Peter, Tuomilehto, Jaakko, Groop, Per-Henrik, Tryggvason, Karl
Published in The American Journal of Human Genetics (2010)

Familial aggregation of atrial fibrillation in Iceland

by Arnar, David O, Thorvaldsson, Sverrir, Manolio, Teri A, Thorgeirsson, Gudmundur, Kristjansson, Kristleifur, Hakonarson, Hakon, Stefansson, Kari
Published in European Heart Journal (2006)

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, 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, CAMPAGNA, MARCELLO
Published in Nature Genetics (2008)

Chromosome 17q-linkage seems to be infrequent in Icelandic families at risk of breast cancer

by Barkardottir, R B, Arason, A, Egilsson, V, Gudmundsson, J, Jonasdottir, A, Johannesdottir, G
Published in Acta Oncologica (2010)

Possible association of a cholecystokinin promotor polymorphism (CCK-36CT) with panic disorder

by Wang, Z, Valdes, J, Noyes, R, Zoega, T, Crowe, R R
Published 2010

Polymorphism of PRNP codons in the normal Icelandic population.

by Georgsson, G, Tryggvason, T, Jonasdottir, A D, Gudmundsson, S, Thorgeirsdottir, S
Published in Acta Neurologica Scandinavica (2007)

An age-associated decrease in the frequency of C4B*Q0 indicates that null alleles of complement may affect health or survival

by Arason, Gudmundur Johann, Bodvarsson, Sigurdur, Sigurdarson, Sigurdur Thor, Sigurdsson, Gardar, Thorgeirsson, Gudmundur, Gudmundsson, Sveinn, Kramer, Judit, Füst, Georg
Published in Annals of the New York Academy of Sciences (2007)

Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype

by Gudmundsson, J, Johannesdottir, G, Arason, A, Bergthorsson, J T, Ingvarsson, S, Egilsson, V, Barkardottir, R B
Published 2010

Prevalence of age-related maculopathy and age-related macular degeneration among the inuit in Greenland. The Greenland Inuit Eye Study

by Andersen, MV, Rosenberg, T, la Cour, M, Kiilgaard, JF, Prause, JU, Alsbirk, PH, Borch-Johnsen, K, Peto, T, Carstensen, B, Bird, AC
Published 2008