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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 أكاديمية
المؤلفون: Helgadottir, Anna, Manolescu, Andrei, Thorleifsson, Gudmar, Gretarsdottir, Solveig, Jonsdottir, Helga, Thorsteinsdottir, Unnur, Samani, Nilesh J, Gudmundsson, Gudmundur, Grant, Struan F A, Thorgeirsson, Gudmundur, Sveinbjornsdottir, Sigurlaug, Valdimarsson, Einar M, Matthiasson, Stefan E, Johannsson, Halldor, Gudmundsdottir, Olof, Gurney, Mark E, Sainz, Jesus, Thorhallsdottir, Margret, Andresdottir, Margret, Frigge, Michael L, Topol, Eric J, Kong, Augustine, Gudnason, Vilmundur, Hakonarson, Hakon, Gulcher, Jeffrey R, Stefansson, Kari
المساهمون: deCODE genetics, Sturlugata 8, Reykjavik, Iceland.
مصطلحات موضوعية: Carrier Proteins, Chromosome Mapping, Chromosomes, Human, Pair 13, Genetic Predisposition to Disease, Humans, Leukotriene B4, Membrane Proteins, Microsatellite Repeats, Myocardial Infarction, Polymorphism, Single Nucleotide, Stroke
العلاقة: http://dx.doi.org/10.1038/ng1311Test; Nat. Genet. 2004, 36(3):233-9; http://hdl.handle.net/2336/56397Test; Nature genetics
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4دورية أكاديمية
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
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5دورية 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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6دورية أكاديمية
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
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7
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 -
8دورية أكاديمية
المؤلفون: Gretarsdottir, Solveig, Thorleifsson, Gudmar, Reynisdottir, Sigridur Th, Manolescu, Andrei, Jonsdottir, Sif, Jonsdottir, Thorbjorg, Gudmundsdottir, Thorunn, Bjarnadottir, Sigrun M, Einarsson, Olafur B, Gudjonsdottir, Herdis M, Hawkins, Malcolm, Gudmundsson, Gudmundur, Gudmundsdottir, Hrefna, Andrason, Hjalti, Gudmundsdottir, Asta S, Sigurdardottir, Matthildur, Chou, Thomas T, Nahmias, Joseph, Goss, Shyamali, Sveinbjornsdottir, Sigurlaug, Valdimarsson, Einar M, Jakobsson, Finnbogi, Agnarsson, Uggi, Gudnason, Vilmundur, Thorgeirsson, Gudmundur, Fingerle, Jurgen, Gurney, Mark, Gudbjartsson, Daniel, Frigge, Michael L, Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R
مصطلحات موضوعية: 3',5'-Cyclic-AMP Phosphodiesterases, 5' Untranslated Regions, Base Sequence, Brain Ischemia, Chromosome Mapping, Chromosomes, Human, Pair 5, Cyclic Nucleotide Phosphodiesterases, Type 3, Type 4, Genetic Predisposition to Disease, Humans, Isoenzymes, Linkage Disequilibrium, Microsatellite Repeats, Molecular Sequence Data, Polymorphism, Genetic, Single Nucleotide
العلاقة: http://dx.doi.org/10.1038/ng1245Test; Nat. Genet. 2003, 35(2):131-8; http://hdl.handle.net/2336/15740Test
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9دورية 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
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10دورية أكاديمية
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