Search Results

Support for involvement of the AHI1 locus in schizophrenia

by Ingason, Andres, Sigmundsson, Thordur, Steinberg, Stacy, Sigurdsson, Engilbert, Haraldsson, Magnus, Magnusdottir, Brynja B, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey, Thorsteinsdottir, Unnur, Stefansson, Kari, Petursson, Hannes, Stefansson, Hreinn
Published in European Journal of Human Genetics (2007)

A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas

by Gudbjartsson, Tomas, Jonasdottir, Thora J, Thoroddsen, Asgeir, Einarsson, Gudmundur V, Jonsdottir, Gudrun M, Kristjansson, Kristleifur, Hardarson, Sverrir, Magnusson, Kjartan, Gulcher, Jeffrey, Stefansson, Kari, Amundadottir, Laufey T
Published in International Journal of Cancer (2008)

Association of vitamin D binding protein variants with chronic mucus hypersecretion in Iceland

by Laufs, Jürgen, Andrason, Hjalti, Sigvaldason, Andres, Halapi, Eva, Thorsteinsson, Leifur, Jónasson, Kristján, Söebech, Emilía, Gislason, Thorarinn, Gulcher, Jeffrey R, Stefansson, Kari, Hakonarson, Hakon
Published 2007

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

by Curran, Sarah, Bolton, Patrick, Rozsnyai, Kinga, Chiocchetti, Andreas, Klauck, Sabine M, Duketis, Eftichia, Poustka, Fritz, Schlitt, Sabine, Freitag, Christine M, Lee, Irene, Muglia, Pierandrea, Poot, Martin, Staal, Wouter, de Jonge, Maretha V, Ophoff, Roel A, Lewis, Cathryn, Skuse, David, Mandy, Will, Vassos, Evangelos, Fossdal, Ragnheidur, Magnusson, Páll, Hreidarsson, Stefan, Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari, Collier, David
Published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics (2012)

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

by Helgason, Agnar, Palsson, Snaebjorn, Thorleifsson, Gudmar, Grant, Struan F A, Emilsson, Valur, Gunnarsdottir, Steinunn, Adeyemo, Adebowale, Chen, Yuanxiu, Chen, Guanjie, Reynisdottir, Inga, Benediktsson, Rafn, Hinney, Anke, Hansen, Torben, Andersen, Gitte, Borch-Johnsen, Knut, Jorgensen, Torben, Schäfer, Helmut, Faruque, Mezbah, Doumatey, Ayo, Zhou, Jie, Wilensky, Robert L, Reilly, Muredach P, Rader, Daniel J, Bagger, Yu, Christiansen, Claus, Sigurdsson, Gunnar, Hebebrand, Johannes, Pedersen, Oluf, Thorsteinsdottir, Unnur, Gulcher, Jeffrey R, Kong, Augustine, Rotimi, Charles, Stefansson, Kari
Published in Nature Genetics (2007)

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)

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)

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)

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)

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)

Variant of TREM2 associated with the risk of Alzheimer's disease.

by Jonsson, Thorlakur, Stefansson, Hreinn, Steinberg, Stacy, Jonsdottir, Ingileif, Jonsson, Palmi V, Snaedal, Jon, Bjornsson, Sigurbjorn, Huttenlocher, Johanna, Levey, Allan I, Lah, James J, Rujescu, Dan, Hampel, Harald, Giegling, Ina, Andreassen, Ole A, Engedal, Knut, Ulstein, Ingun, Djurovic, Srdjan, Ibrahim-Verbaas, Carla, Hofman, Albert, Ikram, M Arfan, van Duijn, Cornelia M, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari
Published in New England Journal of Medicine (2013)

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)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P H, Barnes, Michael R, Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I, Hardarsson, Gudmundur, Jonsdottir, Gudrun A, Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette M, Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A, Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A, Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E, Sabatti, Chiara, Ophoff, Roel A, Rietschel, Marcella, Nöthen, Markus M, Stefansson, Kari, Peltonen, Leena, St Clair, David
Published in Human Molecular Genetics (2011)

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

by Thorleifsson, Gudmar, Walters, G Bragi, Hewitt, Alex W, Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A, Magnusson, Kristinn P, Stefansson, Hreinn, Lam, Dennis S C, Tam, Pancy O S, Gudmundsdottir, Gudrun J, Southgate, Laura, Burdon, Kathryn P, Gottfredsdottir, Maria Soffia, Aldred, Micheala A, Mitchell, Paul, St Clair, David, Collier, David, Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G, Cree, Angela J, Gibson, Jane, Macleod, Alex, Jacob, Aby, Ennis, Sarah, Young, Terri L, Chan, Juliana C N, Karwatowski, Wojciech S S, Hammond, Christopher J, Thordarson, Kristjan, Zhang, Mingzhi, Wadelius, Claes, Lotery, Andrew J, Trembath, Richard C, Pang, Chi Pui, Hoh, Josephine, Craig, Jamie E, Kong, Augustine, Mackey, David A, Jonasson, Fridbert, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

by Thorleifsson, Gudmar, Walters, G Bragi, Hewitt, Alex W, Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A, Magnusson, Kristinn P, Stefansson, Hreinn, Lam, Dennis S C, Tam, Pancy O S, Gudmundsdottir, Gudrun J, Southgate, Laura, Burdon, Kathryn P, Gottfredsdottir, Maria Soffia, Aldred, Micheala A, Mitchell, Paul, St Clair, David, Collier, David A, Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G, Cree, Angela J, Gibson, Jane, Macleod, Alex, Jacob, Aby, Ennis, Sarah, Young, Terri L, Chan, Juliana C N, Karwatowski, Wojciech S S, Hammond, Christopher J, Thordarson, Kristjan, Zhang, Mingzhi, Wadelius, Claes, Lotery, Andrew J, Trembath, Richard C, Pang, Chi Pui, Hoh, Josephine, Craig, Jamie E, Kong, Augustine, Mackey, David A, Jonasson, Fridbert, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

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)

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

by Thorleifsson, Gudmar, Walters, G Bragi, Hewitt, Alex W, Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A, Magnusson, Kristinn P, Stefansson, Hreinn, Lam, Dennis S C, Tam, Pancy O S, Gudmundsdottir, Gudrun J, Southgate, Laura, Burdon, Kathryn P, Gottfredsdottir, Maria Soffia, Aldred, Micheala A, Mitchell, Paul, St Clair, David, Collier, David, Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G, Cree, Angela J, Gibson, Jane, Macleod, Alex, Jacob, Aby, Ennis, Sarah, Young, Terri L, Chan, Juliana C N, Karwatowski, Wojciech S S, Hammond, Christopher J, Thordarson, Kristjan, Zhang, Mingzhi, Wadelius, Claes, Lotery, Andrew J, Trembath, Richard C, Pang, Chi Pui, Hoh, Josephine, Craig, Jamie E, Kong, Augustine, Mackey, David A, Jonasson, Fridbert, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study

by Holm, Hilma, Ivarsdottir, Erna V, Olafsdottir, Thorhildur, Thorolfsdottir, Rosa, Eythorsson, Elias, Norland, Kristjan, Gisladottir, Rosa, Jonsdottir, Gudrun, Unnsteinsdottir, Unnur, Sveinsdottir, Kristin E, Jonsson, Benedikt A, Andresdottir, Margret, Arnar, Davíð Ottó, Arnthorsson, Asgeir O, Birgisdottir, Kolbrún, Bjarnadottir, Kristbjorg, Bjarnadottir, Solveig, Bjornsdottir, Gyda, Einarsson, Gudmundur, Eiriksdottir, Berglind, Gardarsdottir, Elisabet Eir, Gíslason, Þórarinn, Gottfreðsson, Magnús, Gudmundsdottir, Steinunn, Gudmundsson, Julius, Gunnarsdottir, Kristbjorg, Helgadottir, Anna, Helgason, Dadi, Hinriksdottir, Ingibjorg, Ingvarsson, Ragnar Freyr, Jonasdottir, Sigga S, Jónsdóttir, Ingileif, Karlsdottir, Tekla H, Kristinsdottir, Anna M, Kristinsson, Sigurður Yngvi, Kristjansdottir, Steinunn, Löve, Þorvarður Jón, Lúðvíksdóttir, Dóra, Masson, Gisli, Norddahl, Gudmundur, Olafsdottir, Thorunn, Ólafsson, Ísleifur, Rafnar, Thorunn, Runólfsdóttir, Hrafnhildur L., Saemundsdottir, Jona, Sigurbjornsson, Svanur, Sigurdardottir, Kristin, Sigurðsson, Engilbert, Sigurðsson, Martin Ingi, Sigurdsson, Emil L, Steinthorsdottir, Valgerdur, Sveinbjornsson, Gardar, Thorarensen, Emil A, Thorbjornsson, Bjarni, Thorsteinsdottir, Brynja, Tragante, Vinicius, Ulfarsson, Magnus O, Stefansson, Hreinn, Gislason, Thorsteinn, Kristjansson, Mar, Palsson, Runolfur, Sulem, Patrick, Thorsteinsdottir, Unnur, Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Communications Medicine (2023)

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)

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)