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1دورية أكاديمية
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
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2دورية أكاديمية
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
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3دورية أكاديميةCommon variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer
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
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4دورية أكاديمية
المؤلفون: Stacey, Simon N, Manolescu, Andrei, Sulem, Patrick, Rafnar, Thorunn, Gudmundsson, Julius, Gudjonsson, Sigurjon A, Masson, Gisli, Jakobsdottir, Margret, Thorlacius, Steinunn, Helgason, Agnar, Aben, Katja K, Strobbe, Luc J, Albers-Akkers, Marjo T, Swinkels, Dorine W, Henderson, Brian E, Kolonel, Laurence N, Le Marchand, Loic, Millastre, Esther, Andres, Raquel, Godino, Javier, Garcia-Prats, Maria Dolores, Polo, Eduardo, Tres, Alejandro, Mouy, Magali, Saemundsdottir, Jona, Backman, Valgerdur M, Gudmundsson, Larus, Kristjansson, Kristleifur, Bergthorsson, Jon T, Kostic, Jelena, Frigge, Michael L, Geller, Frank, Gudbjartsson, Daniel, Sigurdsson, Helgi, Jonsdottir, Thora, Hrafnkelsson, Jon, Johannsson, Jakob, Sveinsson, Thorarinn, Myrdal, Gardar, Grimsson, Hlynur Niels, Jonsson, Thorvaldur, von Holst, Susanna, Werelius, Barbro, Margolin, Sara, Lindblom, Annika, Mayordomo, Jose I, Haiman, Christopher A, Kiemeney, Lambertus A, Johannsson, Oskar Th, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari
المساهمون: deCODE genetics, Sturlugata 8, 101 Reykjavik, Iceland. simon.stacey@decode.is
مصطلحات موضوعية: Breast Neoplasms, Case-Control Studies, Chromosomes, Human, Pair 16, Pair 2, Female, Genetic Predisposition to Disease, Humans, Receptors, Estrogen, Variation (Genetics)
العلاقة: http://dx.doi.org/10.1038/ng2064Test; Nat. Genet. 2007, 39(7):865-9; http://hdl.handle.net/2336/29981Test; Nature genetics
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5
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 -
6دورية أكاديمية
المؤلفون: 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
مصطلحات موضوعية: African Americans, African Continental Ancestry Group, Case-Control Studies, Epoxide Hydrolases, European Continental Ancestry Group, Genetic Predisposition to Disease, Haplotypes, Humans, Iceland, Linkage Disequilibrium, Molecular Sequence Data, Myocardial Infarction, Variation (Genetics)
العلاقة: http://dx.doi.org/10.1038/ng1692Test; Nat. Genet. 2006, 38(1):68-74; http://hdl.handle.net/2336/15739Test
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7دورية أكاديمية
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
مصطلحات موضوعية: Case-Control Studies, Chromosomes, Human, Pair 17, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, Haplotypes, Hepatocyte Nuclear Factor 1-beta, Polymorphism, Single Nucleotide, Prostatic Neoplasms
وصف الملف: YES
العلاقة: http://dx.doi.org/10.1038/ng2062Test; Nat. Genet. 2007, 39(8):977-83; http://hdl.handle.net/2336/14444Test; Nature genetics