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Your search keyword '"Eyjolfsson, Gudmundur I."' showing total 5 results
Start Over Author "Eyjolfsson, Gudmundur I." Publisher nature publishing group
5 results on '"Eyjolfsson, Gudmundur I."'

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

Author

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, and Stefansson, Kari

Subjects
Mutation (Biology) -- Health aspects, Bones -- Density, Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract

Author(s): Unnur Styrkarsdottir [1]; Gudmar Thorleifsson [1]; Patrick Sulem [1]; Daniel F. Gudbjartsson [1]; Asgeir Sigurdsson [1]; Aslaug Jonasdottir [1]; Adalbjorg Jonasdottir [1]; Asmundur Oddsson [1, 2]; Agnar Helgason [1]; [...]

Published
2013
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2. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

Author

Gudmundsson, Julius, Sigurdsson, Jon K, Stefansdottir, Lilja, Agnarsson, Bjarni A, Isaksson, Helgi J, Stefansson, Olafur A, Gudjonsson, Sigurjon A, Gudbjartsson, Daniel F, Masson, Gisli, Frigge, Michael L, Stacey, Simon N, Sulem, Patrick, Halldorsson, Gisli H, Tragante, Vinicius, Holm, Hilma, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Jonsson, Thorvaldur, Jonsson, Eirikur, Barkardottir, Rosa B, Hilmarsson, Rafn, Geirsson, Gudmundur, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, Stefansson, Kari, Gudmundsson, Julius, Sigurdsson, Jon K, Stefansdottir, Lilja, Agnarsson, Bjarni A, Isaksson, Helgi J, Stefansson, Olafur A, Gudjonsson, Sigurjon A, Gudbjartsson, Daniel F, Masson, Gisli, Frigge, Michael L, Stacey, Simon N, Sulem, Patrick, Halldorsson, Gisli H, Tragante, Vinicius, Holm, Hilma, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Jonsson, Thorvaldur, Jonsson, Eirikur, Barkardottir, Rosa B, Hilmarsson, Rafn, Geirsson, Gudmundur, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, and Stefansson, Kari

Published
2018

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

Author

Onderzoek Precision medicine, Circulatory Health, Team Medisch, Gudmundsson, Julius, Sigurdsson, Jon K, Stefansdottir, Lilja, Agnarsson, Bjarni A, Isaksson, Helgi J, Stefansson, Olafur A, Gudjonsson, Sigurjon A, Gudbjartsson, Daniel F, Masson, Gisli, Frigge, Michael L, Stacey, Simon N, Sulem, Patrick, Halldorsson, Gisli H, Tragante, Vinicius, Holm, Hilma, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Jonsson, Thorvaldur, Jonsson, Eirikur, Barkardottir, Rosa B, Hilmarsson, Rafn, Geirsson, Gudmundur, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, Stefansson, Kari, Onderzoek Precision medicine, Circulatory Health, Team Medisch, Gudmundsson, Julius, Sigurdsson, Jon K, Stefansdottir, Lilja, Agnarsson, Bjarni A, Isaksson, Helgi J, Stefansson, Olafur A, Gudjonsson, Sigurjon A, Gudbjartsson, Daniel F, Masson, Gisli, Frigge, Michael L, Stacey, Simon N, Sulem, Patrick, Halldorsson, Gisli H, Tragante, Vinicius, Holm, Hilma, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Jonsson, Thorvaldur, Jonsson, Eirikur, Barkardottir, Rosa B, Hilmarsson, Rafn, Geirsson, Gudmundur, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, and Stefansson, Kari

Published
2018

4. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Author

Chambers, John C., Zhang, Weihua, Sehmi, Joban, Li, Xinzhong, Wass, Mark N., Van der Harst, Pim, Holm, Hilma, Sanna, Serena, Kavousi, Maryam, Baumeister, Sebastian E., Coin, Lachlan J., Deng, Guohong, Gieger, Christian, Heard-Costa, Nancy L., Hottenga, Jouke-Jan, Kühnel, Brigitte, Kumar, Vinod, Lagou, Vasiliki, Liang, Liming, Luan, Jian'an, Vidal, Pedro Marques, Mateo Leach, Irene, O'Reilly, Paul F., Peden, John F., Rahmioglu, Nilufer, Soininen, Pasi, Speliotes, Elizabeth K., Yuan, Xin, Thorleifsson, Gudmar, Alizadeh, Behrooz Z., Atwood, Larry D., Borecki, Ingrid B., Brown, Morris J., Charoen, Pimphen, Cucca, Francesco, Das, Debashish, de Geus, Eco J. C., Dixon, Anna L., Döring, Angela, Ehret, Georg, Eyjolfsson, Gudmundur I., Farrall, Martin, Forouhi, Nita G., Friedrich, Nele, Goessling, Wolfram, Gudbjartsson, Daniel F., Harris, Tamara B., Hartikainen, Anna-Liisa, Heath, Simon, Hirschfield, Gideon M., Hofman, Albert, Homuth, Georg, Hyppönen, Elina, Janssen, Harry L. A., Johnson, Toby, Kangas, Antti J., Kema, Ido P., Kühn, Jens P., Lai, Sandra, Lathrop, Mark, Lerch, Markus M., Li, Yun, Liang, T. Jake, Lin, Jing-Ping, Loos, Ruth J. F., Martin, Nicholas G., Moffatt, Miriam F., Montgomery, Grant W., Munroe, Patricia B., Musunuru, Kiran, Nakamura, Yusuke, O'Donnell, Christopher J., Olafsson, Isleifur, Penninx, Brenda W., Pouta, Anneli, Prins, Bram P., Prokopenko, Inga, Puls, Ralf, Ruokonen, Aimo, Savolainen, Markku J., Schlessinger, David, Schouten, Jeoffrey N. L., Seedorf, Udo, Sen-Chowdhry, Srijita, Siminovitch, Katherine A., Smit, Johannes H., Spector, Timothy D., Tan, Wenting, Teslovich, Tanya M., Tukiainen, Taru, Uitterlinden, Andre G., Van der Klauw, Melanie M., Vasan, Ramachandran S., Wallace, Chris, Wallaschofski, Henri, Wichmann, H-Erich, Willemsen, Gonneke, Würtz, Peter, Xu, Chun, Yerges-Armstrong, Laura M., Alcohol Genome-wide Association Consortium, Diabetes Genetics Replication, Meta-analyses Study, Genetic Investigation of Anthropometric Traits Consortium, Global Lipids Genetics Consortium, Genetics of Liver Disease Consortium, International Consortium for Blood Pressure, Meta-analyses of Glucose, Insulin-Related Traits Consortium, Abecasis, Goncalo R., Ahmadi, Kourosh R., Boomsma, Dorret I., Caulfield, Mark, Cookson, William O., van Duijn, Cornelia M., Froguel, Philippe, Matsuda, Koichi, McCarthy, Mark I., Meisinger, Christa, Mooser, Vincent, Pietiläinen, Kirsi H., Schumann, Gunter, Snieder, Harold, Sternberg, Michael J. E., Stolk, Ronald P., Thomas, Howard C., Thorsteinsdottir, Unnur, Uda, Manuela, Waeber, Gérard, Wareham, Nicholas J., Waterworth, Dawn M., Watkins, Hugh, Whitfield, John B., Witteman, Jacqueline C. M., Wolffenbuttel, Bruce H. R., Fox, Caroline S., Ala-Korpela, Mika, Stefansson, Kari, Vollenweider, Peter, Völzke, Henry, Schadt, Eric E., Scott, James, Järvelin, Marjo-Riitta, Elliott, Paul, and Kooner, Jaspal S.

Published
2011
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5. Epidemiology of hairy cell leukemia in Iceland.

Author

Kristinsson SY, Vidarsson B, Agnarsson BA, Haraldsdottir V, Olafsson O, Johannesson GM, Eyjolfsson GI, Bjornsdottir J, Onundarson PT, and Reykdal S

Subjects
Adult, Aged, Aged, 80 and over, Female, Follow-Up Studies, Humans, Iceland epidemiology, Incidence, Leukemia, Hairy Cell complications, Leukemia, Hairy Cell mortality, Leukemia, Hairy Cell therapy, Male, Middle Aged, Neoplasms, Second Primary, Remission Induction methods, Retrospective Studies, Leukemia, Hairy Cell epidemiology
Abstract

Introduction: Hairy cell leukemia (HCL) is a rare B-cell lymphoproliferative disorder. Previous epidemiological studies have mainly focused on cases derived from single institutions or from localized cancer registries. This is the first study in which all cases diagnosed nationwide over a long period of time in a well defined population are analysed. We report the epidemiology of all HCL patients in Iceland, their clinical characteristics, treatment and follow-up., Patients and Methods: : All patients diagnosed with HCL in Iceland over a 20 year period, were included in this study. Data was collected retrospectively., Results: Sixteen patients, 13 males and three females were diagnosed with HCL in Iceland from 1981-2000, giving a mean incidence of 4.7/million/year (95% CI: 2.7-7.6) in the population 20 years and older. Eleven patients were treated with a purine analogue, 10 of whom achieved CR. One other patient obtained CR following splenectomy and IFN, giving a total CR rate of 69%. Three other patients (19%) obtained PR, giving a total response rate of 88%. One patient had a variant of HCL and did not respond to any therapy and one patient died of sepsis before any chemotherapy could be given. Six patients with HCL have died, one from complications of HCL. Three patients developed a second malignancy (19%)., Conclusions: The mean incidence of HCL in Iceland is 4.7/million/year. This is slighty higher than the reported incidence in England and Wales, although not significantly higher. The incidence is based on a nationwide information from a well defined stable and racially homogenous island population. Other results are in accordance with previously published studies.

Published
2002
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