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: 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

الإتاحة: https://doi.org/10.1038/ng1311Test
http://hdl.handle.net/2336/56397Test

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: 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

الإتاحة: https://doi.org/10.1038/ng2064Test
http://hdl.handle.net/2336/29981Test

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: 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

الإتاحة: https://doi.org/10.1038/ng1692Test
http://hdl.handle.net/2336/15739Test

المؤلفون: Gudmundsson, Julius, Sulem, Patrick, Manolescu, Andrei, Amundadottir, Laufey T, Gudbjartsson, Daniel, Helgason, Agnar, Rafnar, Thorunn, Bergthorsson, Jon T, Agnarsson, Bjarni A, Baker, Adam, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Jakobsdottir, Margret, Xu, Jianfeng, Blondal, Thorarinn, Kostic, Jelena, Sun, Jielin, Ghosh, Shyamali, Stacey, Simon N, Mouy, Magali, Saemundsdottir, Jona, Backman, Valgerdur M, Kristjansson, Kristleifur, Tres, Alejandro, Partin, Alan W, Albers-Akkers, Marjo T, Godino-Ivan Marcos, Javier, Walsh, Patrick C, Swinkels, Dorine W, Navarrete, Sebastian, Isaacs, Sarah D, Aben, Katja K, Graif, Theresa, Cashy, John, Ruiz-Echarri, Manuel, Wiley, Kathleen E, Suarez, Brian K, Witjes, J Alfred, Frigge, Mike, Ober, Carole, Jonsson, Eirikur, Einarsson, Gudmundur V, Mayordomo, Jose I, Kiemeney, Lambertus A, Isaacs, William B, Catalona, William J, Barkardottir, Rosa B, Gulcher, Jeffrey R, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

مصطلحات موضوعية: PubMed - in process

وصف الملف: YES

العلاقة: http://dx.doi.org/10.1038/ng1999Test; Nat. Genet. 2007, 39(5):631-7; http://hdl.handle.net/2336/14522Test

الإتاحة: https://doi.org/10.1038/ng1999Test
http://hdl.handle.net/2336/14522Test

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

الإتاحة: https://doi.org/10.1038/ng2062Test
http://hdl.handle.net/2336/14444Test

المؤلفون: Grant, Struan F A, Thorleifsson, Gudmar, Reynisdottir, Inga, Benediktsson, Rafn, Manolescu, Andrei, Sainz, Jesus, Helgason, Agnar, Stefansson, Hreinn, Emilsson, Valur, Helgadottir, Anna, Styrkarsdottir, Unnur, Magnusson, Kristinn P, Walters, G Bragi, Palsdottir, Ebba, Jonsdottir, Thorbjorg, Gudmundsdottir, Thorunn, Gylfason, Arnaldur, Saemundsdottir, Jona, Wilensky, Robert L, Reilly, Muredach P, Rader, Daniel J, Bagger, Yu, Christiansen, Claus, Gudnason, Vilmundur, Sigurdsson, Gunnar, Thorsteinsdottir, Unnur, Gulcher, Jeffrey R, Kong, Augustine, Stefansson, Kari

المساهمون: deCODE genetics, Sturlugata 8, 101 Reykjavik, Iceland. struan.grant@decode.is

مصطلحات موضوعية: Chromosome Mapping, Chromosomes, Human, Pair 10, Cohort Studies, Denmark, Diabetes Mellitus, Type 2, Gene Frequency, Genetic Predisposition to Disease, Heterozygote Detection, Humans, Introns, Microsatellite Repeats, Molecular Sequence Data, Reference Values, TCF Transcription Factors

العلاقة: http://dx.doi.org/10.1038/ng1732Test; Nat. Genet. 2006, 38(3):320-3; http://hdl.handle.net/2336/18698Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng1732Test
http://hdl.handle.net/2336/18698Test

المؤلفون: Amundadottir, Laufey T, Sulem, Patrick, Gudmundsson, Julius, Helgason, Agnar, Baker, Adam, Agnarsson, Bjarni A, Sigurdsson, Asgeir, Benediktsdottir, Kristrun R, Cazier, Jean-Baptiste, Sainz, Jesus, Jakobsdottir, Margret, Kostic, Jelena, Magnusdottir, Droplaug N, Ghosh, Shyamali, Agnarsson, Kari, Birgisdottir, Birgitta, Le Roux, Louise, Olafsdottir, Adalheidur, Blondal, Thorarinn, Andresdottir, Margret, Gretarsdottir, Olafia Svandis, Bergthorsson, Jon T, Gudbjartsson, Daniel, Gylfason, Arnaldur, Thorleifsson, Gudmar, Manolescu, Andrei, Kristjansson, Kristleifur, Geirsson, Gudmundur, Isaksson, Helgi, Douglas, Julie, Johansson, Jan-Erik, Bälter, Katarina, Wiklund, Fredrik, Montie, James E, Yu, Xiaoying, Suarez, Brian K, Ober, Carole, Cooney, Kathleen A, Gronberg, Henrik, Catalona, William J, Einarsson, Gudmundur V, Barkardottir, Rosa B, Gulcher, Jeffrey R, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari

مصطلحات موضوعية: African Continental Ancestry Group, Alleles, European Continental Ancestry Group, Male, Microsatellite Repeats, Polymorphism, Single Nucleotide, Prostatic Neoplasms, Research Support, N.I.H., Extramural, Non-U.S. Gov't

وصف الملف: YES

العلاقة: http://www.nature.com/ng/journal/v38/n6/full/ng1808.htmlTest; Nat. Genet. 2006, 38(6):652-8; PTT12; URO12; http://hdl.handle.net/2336/6357Test

الإتاحة: https://doi.org/10.1038/ng1808Test
http://hdl.handle.net/2336/6357Test