المؤلفون: Helgadottir, Anna, Thorleifsson, Gudmar, Magnusson, Kristinn P, Gretarsdottir, Solveig, Steinthorsdottir, Valgerdur, Manolescu, Andrei, Jones, Gregory T, Rinkel, Gabriel J E, Blankensteijn, Jan D, Ronkainen, Antti, Jääskeläinen, Juha E, Kyo, Yoshiki, Lenk, Guy M, Sakalihasan, Natzi, Kostulas, Konstantinos, Gottsäter, Anders, Flex, Andrea, Stefansson, Hreinn, Hansen, Torben, Andersen, Gitte, Weinsheimer, Shantel, Borch-Johnsen, Knut, Jorgensen, Torben, Shah, Svati H, Quyyumi, Arshed A, Granger, Christopher B, Reilly, Muredach P, Austin, Harland, Levey, Allan I, Vaccarino, Viola, Palsdottir, Ebba, Walters, G Bragi, Jonsdottir, Thorbjorg, Snorradottir, Steinunn, Magnusdottir, Dana, Gudmundsson, Gudmundur, Ferrell, Robert E, Sveinbjornsdottir, Sigurlaug, Hernesniemi, Juha, Niemelä, Mika, Limet, Raymond, Andersen, Karl, Sigurdsson, Gunnar, Benediktsson, Rafn, Verhoeven, Eric L G, Teijink, Joep A W, Grobbee, Diederick E, Rader, Daniel J, Collier, David A, Pedersen, Oluf, Pola, Roberto, Hillert, Jan, Lindblad, Bengt, Valdimarsson, Einar M, Magnadottir, Hulda B, Wijmenga, Cisca, Tromp, Gerard, Baas, Annette F, Ruigrok, Ynte M, van Rij, Andre M, Kuivaniemi, Helena, Powell, Janet T, Matthiasson, Stefan E, Gulcher, Jeffrey R, Thorgeirsson, Gudmundur, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari

المساهمون: deCODE Genetics, Sturlugata 8, IS-101 Reykjavik, Iceland.

مصطلحات موضوعية: Adult, Aged, Alleles, Aortic Aneurysm, Abdominal, Case-Control Studies, Chi-Square Distribution, Chromosomes, Human, Pair 9, European Continental Ancestry Group, Female, Gene Frequency, Genetic Markers, Genetic Variation, Haplotypes, Homozygote, Humans, Intracranial Aneurysm, Likelihood Functions, Linkage Disequilibrium, Male, Middle Aged, Myocardial Infarction, Odds Ratio, Polymorphism, Single Nucleotide, Prevalence, Probability, Risk Factors

العلاقة: http://dx.doi.org/10.1038/ng.72Test; Nat. Genet. 2008, 40(2):217-24; http://hdl.handle.net/2336/127408Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.72Test
http://hdl.handle.net/2336/127408Test

المؤلفون: Gudmundsson, Julius, Sulem, Patrick, Rafnar, Thorunn, Bergthorsson, Jon T, Manolescu, Andrei, Gudbjartsson, Daniel, Agnarsson, Bjarni A, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Blondal, Thorarinn, Jakobsdottir, Margret, Stacey, Simon N, Kostic, Jelena, Kristinsson, Kari T, Birgisdottir, Birgitta, Ghosh, Shyamali, Magnusdottir, Droplaug N, Thorlacius, Steinunn, Thorleifsson, Gudmar, Zheng, S Lilly, Sun, Jielin, Chang, Bao-Li, Elmore, J Bradford, Breyer, Joan P, McReynolds, Kate M, Bradley, Kevin M, Yaspan, Brian L, Wiklund, Fredrik, Stattin, Par, Lindström, Sara, Adami, Hans-Olov, McDonnell, Shannon K, Schaid, Daniel J, Cunningham, Julie M, Wang, Liang, Cerhan, James R, St Sauver, Jennifer L, Isaacs, Sara D, Wiley, Kathleen E, Partin, Alan W, Walsh, Patrick C, Polo, Sonia, Ruiz-Echarri, Manuel, Navarrete, Sebastian, Fuertes, Fernando, Saez, Berta, Godino, Javier, Weijerman, Philip C, Swinkels, Dorine W, Aben, Katja K, Witjes, J Alfred, Suarez, Brian K, Helfand, Brian T, Frigge, Michael L, Kristjansson, Kristleifur, Ober, Carole, Jonsson, Eirikur, Einarsson, Gudmundur V, Xu, Jianfeng, Gronberg, Henrik, Smith, Jeffrey R, Thibodeau, Stephen N, Isaacs, William B, Catalona, William J, Mayordomo, Jose I, Kiemeney, Lambertus A, Barkardottir, Rosa B, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

المساهمون: deCODE genetics, 101 Reykjavik, Iceland. julius@decode.is

مصطلحات موضوعية: Case-Control Studies, Chromosomes, Human, Pair 2, Gene Frequency, Genetic Predisposition to Disease, Genetic Screening, Humans, Iceland, Linkage Disequilibrium, Male, Netherlands, Polymorphism, Single Nucleotide, Prostatic Neoplasms, Spain, Sweden, United States

العلاقة: http://dx.doi.org/10.1038/ng.89Test; Nat. Genet. 2008, 40(3):281-3; http://hdl.handle.net/2336/87460Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.89Test
http://hdl.handle.net/2336/87460Test

المؤلفون: Hakonarson, Hakon, Thorvaldsson, Sverrir, Helgadottir, Anna, Gudbjartsson, Daniel, Zink, Florian, Andresdottir, Margret, Manolescu, Andrei, Arnar, David O, Andersen, Karl, Sigurdsson, Axel, Thorgeirsson, Gestur, Jonsson, Asgeir, Agnarsson, Uggi, Bjornsdottir, Halldora, Gottskalksson, Gizur, Einarsson, Atli, Gudmundsdottir, Hrefna, Adalsteinsdottir, Asdis E, Gudmundsson, Kolbeinn, Kristjansson, Kristleifur, Hardarson, Thordur, Kristinsson, Arni, Topol, Eric J, Gulcher, Jeffrey, Kong, Augustine, Gurney, Mark, Thorgeirsson, Gudmundur, Stefansson, Kari

المساهمون: Decode Genetics Inc, Reykjavik, Iceland. hakonh@decode.is

مصطلحات موضوعية: Aged, Biological Markers, Carrier Proteins, Coronary Artery Disease, Cross-Over Studies, Epoxide Hydrolases, Female, Humans, Leukotriene B4, Leukotriene E4, Lipoxygenase Inhibitors, Male, Membrane Proteins, Middle Aged, Myocardial Infarction, Peroxidase, Polymorphism, Single Nucleotide, Prospective Studies, Quinolines, Risk Factors

العلاقة: http://jama.ama-assn.org/cgi/content/abstract/293/18/2245Test; JAMA. 2005, 293(18):2245-56; http://hdl.handle.net/2336/53793Test; JAMA : the journal of the American Medical Association

الإتاحة: https://doi.org/10.1001/jama.293.18.2245Test
http://hdl.handle.net/2336/53793Test

المؤلفون: Stacey, Simon N, Manolescu, Andrei, Sulem, Patrick, Thorlacius, Steinunn, Gudjonsson, Sigurjon A, Jonsson, Gudbjorn F, Jakobsdottir, Margret, Bergthorsson, Jon T, Gudmundsson, Julius, Aben, Katja K, Strobbe, Luc J, Swinkels, Dorine W, van Engelenburg, K C Anton, Henderson, Brian E, Kolonel, Laurence N, Le Marchand, Loic, Millastre, Esther, Andres, Raquel, Saez, Berta, Lambea, Julio, Godino, Javier, Polo, Eduardo, Tres, Alejandro, Picelli, Simone, Rantala, Johanna, Margolin, Sara, Jonsson, Thorvaldur, Sigurdsson, Helgi, Jonsdottir, Thora, Hrafnkelsson, Jon, Johannsson, Jakob, Sveinsson, Thorarinn, Myrdal, Gardar, Grimsson, Hlynur Niels, Sveinsdottir, Steinunn G, Alexiusdottir, Kristin, Saemundsdottir, Jona, Sigurdsson, Asgeir, Kostic, Jelena, Gudmundsson, Larus, Kristjansson, Kristleifur, Masson, Gisli, Fackenthal, James D, Adebamowo, Clement, Ogundiran, Temidayo, Olopade, Olufunmilayo I, Haiman, Christopher A, Lindblom, Annika, Mayordomo, Jose I, Kiemeney, Lambertus A, Gulcher, Jeffrey R, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Johannsson, Oskar T, Kong, Augustine, Stefansson, Kari

المساهمون: deCODE Genetics, Sturlugata 8, 101 Reykjavik, Iceland. simon.stacey@decode.is

مصطلحات موضوعية: Adenocarcinoma, Adult, Aged, 80 and over, Apoptosis, Breast Neoplasms, Carcinoma, Ductal, Breast, Intraductal, Noninfiltrating, Lobular, Medullary, Case-Control Studies, Chromosomes, Human, Pair 5, Cohort Studies, Female, Genetic Predisposition to Disease, Humans, International Agencies, Male, Middle Aged, Polymorphism, Single Nucleotide, Prognosis, Receptor, Fibroblast Growth Factor, Type 2

العلاقة: http://dx.doi.org/10.1038/ng.131Test; Nat. Genet. 2008, 40(6):703-6; http://hdl.handle.net/2336/42361Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.131Test
http://hdl.handle.net/2336/42361Test

المؤلفون: Kristjansson, Kristleifur, Manolescu, Andrei, Kristinsson, Arni, Hardarson, Thordur, Knudsen, Helga, Ingason, Sigurdur, Thorleifsson, Gudmar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefansson, Kari

المساهمون: deCODE genetics, Inc, Reykjavik, Iceland. kris@ decode.is

مصطلحات موضوعية: Adult, Aged, Chromosomes, Human, Pair 18, Family Health, Female, Genetic Predisposition to Disease, Genome, Humans, Hypertension, Iceland, Linkage (Genetics), Male, Middle Aged

العلاقة: http://hyper.ahajournals.org/cgi/content/abstract/39/6/1044Test; Hypertension. 2002, 39(6):1044-9; http://hdl.handle.net/2336/32052Test; Hypertension

الإتاحة: http://hdl.handle.net/2336/32052Test

المؤلفون: 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

المساهمون: deCODE Genetics, Reykjavik, Iceland. kstefans@decode.is.

مصطلحات موضوعية: Animals, Chromosome Mapping, Chromosomes, Human, Pair 8, Disease Models, Animal, Female, Genetic Predisposition to Disease, Haplotypes, Humans, Male, Mice, Inbred C57BL, Molecular Sequence Data, Neuregulin-1, Receptor, Epidermal Growth Factor, Schizophrenia

العلاقة: http://www.sciencedirect.com/science/article/B8JDD-4PYSFD6-J/1/d8488e3081ae23e30a31f6b1ec48865aTest; Am. J. Hum. Genet. 2002, 71(4):877-92; http://hdl.handle.net/2336/31233Test; American journal of human genetics

الإتاحة: https://doi.org/10.1086/342734Test
http://hdl.handle.net/2336/31233Test

المؤلفون: Sulem, Patrick, Gudbjartsson, Daniel F, Stacey, Simon N, Helgason, Agnar, Rafnar, Thorunn, Magnusson, Kristinn P, Manolescu, Andrei, Karason, Ari, Palsson, Arnar, Thorleifsson, Gudmar, Jakobsdottir, Margret, Steinberg, Stacy, Pálsson, Snaebjörn, Jonasson, Fridbert, Sigurgeirsson, Bardur, Thorisdottir, Kristin, Ragnarsson, Rafn, Benediktsdottir, Kristrun R, Aben, Katja K, Kiemeney, Lambertus A, Olafsson, Jon H, Gulcher, Jeffrey, Kong, Augie, Thorsteinsdottir, Unnur, Stefansson, Kari

المساهمون: deCODE genetics, Sturlugata 8, 101 Reykjavik, Iceland.

مصطلحات موضوعية: Antiporters, European Continental Ancestry Group, Eye Color, Female, Hair Color, Iceland, Male, Membrane Transport Proteins, Monophenol Monooxygenase, Netherlands, Polymorphism, Single Nucleotide, Receptor, Melanocortin, Type 1, Skin Pigmentation, Stem Cell Factor

العلاقة: http://dx.doi.org/10.1038/ng.2007.13Test; Nat Genet. 2007, 39 (12):1443-52; http://hdl.handle.net/2336/15572Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.2007.13Test
http://hdl.handle.net/2336/15572Test

المؤلفون: Gudmundsson, Julius, Sulem, Patrick, Rafnar, Thorunn, Bergthorsson, Jon T, Manolescu, Andrei, Gudbjartsson, Daniel, Agnarsson, Bjarni A, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Blondal, Thorarinn, Jakobsdottir, Margret, Stacey, Simon N, Kostic, Jelena, Kristinsson, Kari T, Birgisdottir, Birgitta, Ghosh, Shyamali, Magnusdottir, Droplaug N, Thorlacius, Steinunn, Thorleifsson, Gudmar, Zheng, S Lilly, Sun, Jielin, Chang, Bao-Li, Elmore, J Bradford, Breyer, Joan P, McReynolds, Kate M, Bradley, Kevin M, Yaspan, Brian L, Wiklund, Fredrik, Stattin, Pär, Lindström, Sara, Adami, Hans-Olov, McDonnell, Shannon K, Schaid, Daniel J, Cunningham, Julie M, Wang, Liang, Cerhan, James R, St Sauver, Jennifer L, Isaacs, Sara D, Wiley, Kathleen E, Partin, Alan W, Walsh, Patrick C, Polo, Sonia, Ruiz-Echarri, Manuel, Navarrete, Sebastian, Fuertes, Fernando, Saez, Berta, Godino, Javier, Weijerman, Philip C, Swinkels, Dorine W, Aben, Katja K, Witjes, J Alfred, Suarez, Brian K, Helfand, Brian T, Frigge, Michael L, Kristjansson, Kristleifur, Ober, Carole, Jonsson, Eirikur, Einarsson, Gudmundur V, Xu, Jianfeng, Gronberg, Henrik, Smith, Jeffrey R, Thibodeau, Stephen N, Isaacs, William B, Catalona, William J, Mayordomo, Jose I, Kiemeney, Lambertus A, Barkardottir, Rosa B, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

المصدر: Nat Genet. 40(3):281-3

مصطلحات موضوعية: Case-Control Studies, Chromosomes, Human, Pair 2, Gene Frequency, Genetic Predisposition to Disease, Genetic Screening, Humans, Iceland, Linkage Disequilibrium, Male, Netherlands, Polymorphism, Single Nucleotide, Prostatic Neoplasms/*genetics, Spain, Sweden, United States

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-10337Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=18264098&dopt=CitationTest

المؤلفون: Helgadottir, Anna, Thorleifsson, Gudmar, Manolescu, Andrei, Gretarsdottir, Solveig, Blondal, Thorarinn, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Sigurdsson, Asgeir, Baker, Adam, Palsson, Arnar, Masson, Gisli, Gudbjartsson, Daniel F, Magnusson, Kristinn P, Andersen, Karl, Levey, Allan I, Backman, Valgerdur M, Matthiasdottir, Sigurborg, Jonsdottir, Thorbjorg, Palsson, Stefan, Einarsdottir, Helga, Gunnarsdottir, Steinunn, Gylfason, Arnaldur, Vaccarino, Viola, Hooper, W Craig, Reilly, Muredach P, Granger, Christopher B, Austin, Harland, Rader, Daniel J, Shah, Svati H, Quyyumi, Arshed A, Gulcher, Jeffrey R, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

مصطلحات موضوعية: Variation (Genetics), Risk Factors, Polymorphism, Single Nucleotide, Myocardial Infarction, Middle Aged, Male, Linkage Disequilibrium, Humans, Homozygote, Haplotypes, Genotype, Genetic Predisposition to Disease, Genes, p16, Coronary Arteriosclerosis, Chromosomes, Human, Pair 9, Chromosome Mapping, Age of Onset

وصف الملف: YES

العلاقة: http://www.sciencemag.org/cgi/content/full/316/5830/1491Test; Science 2007, 316(5830):1491-3; http://hdl.handle.net/2336/12494Test

الإتاحة: https://doi.org/10.1126/science.1142842Test
http://hdl.handle.net/2336/12494Test

المؤلفون: Gudmundsson, Julius, Sulem, Patrick, Steinthorsdottir, Valgerdur, Bergthorsson, Jon T, Thorleifsson, Gudmar, Manolescu, Andrei, Rafnar, Thorunn, Gudbjartsson, Daniel, Agnarsson, Bjarni A, Baker, Adam, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Jakobsdottir, Margret, Blondal, Thorarinn, Stacey, Simon N, Helgason, Agnar, Gunnarsdottir, Steinunn, Olafsdottir, Adalheidur, Kristinsson, Kari T, Birgisdottir, Birgitta, Ghosh, Shyamali, Thorlacius, Steinunn, Magnusdottir, Dana, Stefansdottir, Gerdur, Kristjansson, Kristleifur, Bagger, Yu, Wilensky, Robert L, Reilly, Muredach P, Morris, Andrew D, Kimber, Charlotte H, Adeyemo, Adebowale, Chen, Yuanxiu, Zhou, Jie, So, Wing-Yee, Tong, Peter C Y, Ng, Maggie C Y, Hansen, Torben, Andersen, Gitte, Borch-Johnsen, Knut, Jorgensen, Torben, Tres, Alejandro, Fuertes, Fernando, Ruiz-Echarri, Manuel, Asin, Laura, Saez, Berta, van Boven, Erica, Klaver, Siem, Swinkels, Dorine W, Aben, Katja K, Graif, Theresa, Cashy, John, Suarez, Brian K, van Vierssen Trip, Onco, Frigge, Michael L, Ober, Carole, Hofker, Marten H, Wijmenga, Cisca, Christiansen, Claus, Rader, Daniel J, Palmer, Colin N A, Rotimi, Charles, Chan, Juliana C N, Pedersen, Oluf, Sigurdsson, Gunnar, Benediktsson, Rafn, Jonsson, Eirikur, Einarsson, Gudmundur V, Mayordomo, Jose I, Catalona, William J, Kiemeney, Lambertus A, Barkardottir, Rosa B, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

المصدر: Gudmundsson , J , Sulem , P , Steinthorsdottir , V , Bergthorsson , J T , Thorleifsson , G , Manolescu , A , Rafnar , T , Gudbjartsson , D , Agnarsson , B A , Baker , A , Sigurdsson , A , Benediktsdottir , K R , Jakobsdottir , M , Blondal , T , Stacey , S N , Helgason , A , Gunnarsdottir , S , Olafsdottir , A , Kristinsson , K T , Birgisdottir , B , Ghosh , S , Thorlacius , S , Magnusdottir , D , Stefansdottir , ....

مصطلحات موضوعية: Case-Control Studies, Chromosomes, Human, Pair 17, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, Haplotypes, Hepatocyte Nuclear Factor 1-beta, Humans, Male, Polymorphism, Single Nucleotide, Prostatic Neoplasms

الإتاحة: https://doi.org/10.1038/ng2062Test
https://curis.ku.dk/portal/da/publications/two-variants-on-chromosome-17-confer-prostate-cancer-risk-and-the-one-in-tcf2-protects-against-type-2-diabetesTest(20979a80-20ec-11dd-bc23-000ea68e967b).html