المؤلفون: Couch, Fergus J, Wang, Xianshu, McGuffog, Lesley, Lee, Andrew, Olswold, Curtis, Kuchenbaecker, Karoline B, Soucy, Penny, Fredericksen, Zachary, Barrowdale, Daniel, Dennis, Joe, Gaudet, Mia M, Simard, Jacques, Pastinen, Tomi, Pankratz, Vernon S, Offit, Kenneth, Easton, Douglas F, Singer, Christian F, Chenevix-Trench, Georgia, Antoniou, Antonis C, Friedman, Eitan, McCann, Emma, Gschwantler-Kaulich, Daphne, Thomassen, Mads, Hansen, Thomas V O, Neuhausen, Susan L, Szabo, Csilla I, Blanco, Ignacio, Greene, Mark H, Karlan, Beth Y, Garber, Judy, Phelan, Catherine M, Weitzel, Jeffrey N, Pfeiler, Georg, Murray, Alex, Montagna, Marco, Olah, Edith, Andrulis, Irene L, Godwin, Andrew K, Yannoukakos, Drakoulis, Goldgar, David E, Caldes, Trinidad, Nevanlinna, Heli, Osorio, Ana, Tea, Muy-Kheng, Terry, Mary Beth, Dicks, Ed, Daly, Mary B, van Rensburg, Elizabeth J, Hamann, Ute, Ramus, Susan J, Toland, Amanda Ewart, Caligo, Maria A, Olopade, Olufunmilayo I, Tung, Nadine, Lindor, Noralane M, Claes, Kathleen, Beattie, Mary S, Calender, Alain, Southey, Melissa C, Imyanitov, Evgeny N, Tischkowitz, Marc, Janavicius, Ramunas, John, Esther M, Kwong, Ava, Diez, Orland, Kaufman, Bella, Balmaña, Judith, Barkardottir, Rosa B, Arun, Banu K, Hardouin, Agnès, Rennert, Gad, Teo, Soo-Hwang, Ganz, Patricia A, Campbell, Ian, van der Hout, Annemarie H, van Deurzen, Carolien H M, Shimon Paluch, Shani, Seynaeve, Caroline, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Berthet, Pascaline, Gille, Johannes J P, Ausems, Margreet G E M, Blok, Marinus J, Ligtenberg, Marjolijn J L, Rookus, Matti A, Laitman, Yael, Devilee, Peter, Verhoef, Senno, van Os, Theo A M, Wijnen, Juul T, Frost, Debra, Delnatte, Capucine, Ellis, Steve, Fineberg, Elena, Platte, Radka, Evans, D Gareth, Skytte, Anne-Bine, Izatt, Louise, Eeles, Rosalind A, Adlard, Julian, Eccles, Diana M, Cook, Jackie, Brewer, Carole, Nogues, Catherine, Douglas, Fiona, Hodgson, Shirley, Lasset, Christine, Gerdes, Anne-Marie, Houdayer, Claude, Leroux, Dominique, Rouleau, Etienne, Prieur, Fabienne, Kosel, Matthew, Damiola, Francesca, Sobol, Hagay, Coupier, Isabelle, Venat-Bouvet, Laurence, Castera, Laurent, Peock, Susan, Gauthier-Villars, Marion, Léoné, Mélanie, Pujol, Pascal, Mazoyer, Sylvie, Bignon, Yves-Jean, Healey, Sue, Złowocka-Perłowska, Elżbieta, Gronwald, Jacek, Lubinski, Jan, Durda, Katarzyna, Morrison, Patrick J, Jaworska, Katarzyna, Huzarski, Tomasz, Spurdle, Amanda B, Viel, Alessandra, Peissel, Bernard, Bonanni, Bernardo, Sinilnikova, Olga M, Melloni, Giulia, Ottini, Laura, Papi, Laura, Pedersen, Inge Sokilde, Varesco, Liliana, Tibiletti, Maria Grazia, Peterlongo, Paolo, Volorio, Sara, Manoukian, Siranoush, Pensotti, Valeria, Arnold, Norbert, Lee, Adam, Engel, Christoph, Deissler, Helmut, Moeller, Sanne Traasdahl, Gadzicki, Dorothea, Gehrig, Andrea, Kast, Karin, Rhiem, Kerstin, Meindl, Alfons, Niederacher, Dieter, Ditsch, Nina, Plendl, Hansjoerg, Bacot, François, Preisler-Adams, Sabine, Kruse, Torben A, Engert, Stefanie, Sutter, Christian, Varon-Mateeva, Raymonda, Wappenschmidt, Barbara, Weber, Bernhard H F, Arver, Brita, Stenmark-Askmalm, Marie, Loman, Niklas, Rosenquist, Richard, Vincent, Daniel, Jensen, Uffe Birk, Einbeigi, Zakaria, Nathanson, Katherine L, Rebbeck, Timothy R, Blank, Stephanie V, Cohn, David E, Rodriguez, Gustavo C, Small, Laurie, Friedlander, Michael, Bae-Jump, Victoria L, Fink-Retter, Anneliese, Vijai, Joseph, Hogervorst, Frans B L, Rappaport, Christine, Sarrel, Kara, Robson, Mark, Kauff, Noah, Mulligan, Anna Marie, Glendon, Gord, Side, Lucy E, Stoppa-Lyonnet, Dominique, Ozcelik, Hilmi, Ejlertsen, Bent, Nielsen, Finn C, Jønson, Lars, Andersen, Mette K, Ding, Yuan Chun, Steele, Linda, Foretova, Lenka, Teulé, Alex, Donaldson, Alan, Lazaro, Conxi, Jakubowska, Anna, Brunet, Joan, Pujana, Miquel Angel, Mai, Phuong L, Loud, Jennifer T, Walsh, Christine, Lester, Jenny, Orsulic, Sandra, Narod, Steven A, Houghton, Catherine, Herzog, Josef, Sand, Sharon R, Radice, Paolo, Tognazzo, Silvia, Agata, Simona, Vaszko, Tibor, Weaver, Joellen, Stavropoulou, Alexandra V, Buys, Saundra S, Romero, Atocha, Rogers, Mark T, de la Hoya, Miguel, Aittomäki, Kristiina, Muranen, Taru A, Schmutzler, Rita Katharina, Duran, Mercedes, Chung, Wendy K, Lasa, Adriana, Dorfling, Cecilia M, Miron, Alexander, Benitez, Javier, Dorkins, Huw, Senter, Leigha, Huo, Dezheng, Chan, Salina B, Sokolenko, Anna P, Domchek, Susan M, Chiquette, Jocelyne, Tihomirova, Laima, Friebel, Tara M, Agnarsson, Bjarni A, Lu, Karen H, Eason, Jacqueline, Lejbkowicz, Flavio, James, Paul A, Hall, Per, Dunning, Alison M, Tessier, Daniel, Piedmonte, Marion, Cunningham, Julie, Slager, Susan L, Wang, Chen, Hart, Steven, Gregory, Helen, Stevens, Kristen

المساهمون: Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA, Mayo Clin, Rochester, MN USA, Univ Cambridge, Ctr Canc Genet Epidemiol, Dept Publ Hlth & Primary Care, Cambridge, England, Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA, Ctr Hosp Univ Quebec, Canc Genom Lab, Quebec City, PQ, Canada, Univ Laval, Quebec City, PQ, Canada, Amer Canc Soc, Epidemiol Res Program, Atlanta, GA 30329 USA, Queensland Inst Med Res, Dept Genet, Brisbane, Qld 4006, Australia, Hosp Civils Lyon, Unite Mixte Genet Constitut Canc Frequents, Ctr Leon Berard, Lyon, France, Univ Lyon 1, INSERM U1052, CNRS UMR5286, Ctr Rech Cancerol Lyon, F-69365 Lyon, France, Mayo Clin, Dept Mol Pharmacol & Expt Therapeut MPET, Rochester, MN USA, Ctr Innovat Genome Quebec, Montreal, PQ, Canada, McGill Univ, Montreal, PQ, Canada, Netherlands Canc Inst, Family Canc Clin, Amsterdam, Netherlands, Inst Curie, Dept Tumour Biol, Paris, France, Inst Curie, INSERM U830, Paris, France, Univ Paris 05, Sorbonne Paris Cite, Paris, France, Pomeranian Med Univ, Dept Genet & Pathol, Szczecin, Poland, Peter MacCallum Canc Ctr, Kathleen Cuningham Consortium Res Familial Breast, Melbourne, Vic, Australia, Fdn IRCCS Ist Nazl Tumori INT, Unit Mol Bases Genet Risk & Genet Testing, Dept Prevent & Predict Med, Milan, Italy, Fdn Ist FIRC Oncol Mol, IFOM, Milan, Italy, Univ Hosp Cologne, Ctr Familial Breast & Ovarian Canc, Dept Obstet & Gynaecol, Cologne, Germany, Univ Hosp Cologne, Ctr Integrated Oncol, Ctr Mol Med Cologne, Cologne, Germany, Lund Univ, Dept Oncol, Lund, Sweden, Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA, Roswell Pk Canc Inst, Gynecol Oncol Grp, Stat & Data Ctr, Buffalo, NY 14263 USA, Med Univ Vienna, Dept Obstet & Gynecol, Vienna, Austria, Med Univ Vienna, Ctr Comprehens Canc, Vienna, Austria, Chaim Sheba Med Ctr, Tel Aviv, Israel, Odense Univ Hosp, Dept Clin Genet, DK-5000 Odense, Denmark, Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada, Copenhagen Univ Hosp, Ctr Genom Med, Rigshosp, Copenhagen, Denmark, City Hope Natl Med Ctr, Dept Populat Sci, Beckman Res Inst, Duarte, CA USA, Univ Delaware, Ctr Translat Canc Res, Dept Biol Sci, Newark, DE USA, IDIBELL Catalan Inst Oncol, Genet Counseling Unit, Hereditary Canc Program, Barcelona, Spain, IDIBGI Catalan Inst Oncol, Genet Counseling Unit, Hereditary Canc Program, Girona, Spain, IDIBELL Catalan Inst Oncol, Translat Res Lab, Breast Canc & Syst Biol Unit, Barcelona, Spain, Univ Toronto, Womens Coll Res Inst, Toronto, ON, Canada, Fox Chase Canc Ctr, Philadelphia, PA 19111 USA, Univ Utah, Sch Med, Dept Internal Med, Huntsman Canc Inst, Salt Lake City, UT USA, Univ Helsinki, Cent Hosp, Dept Clin Genet, Helsinki, Finland, Univ Valladolid IBGM UVA, Inst Biol & Mol Genet, Valladolid, Spain, Columbia Univ, Dept Pediat, New York, NY 10027 USA, Hosp Santa Creu & Sant Pau, Genet Serv, Barcelona, Spain, Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA, Canc Prevent Inst Calif, Breast Canc Family Registry, Fremont, CA USA, Spanish Natl Canc Ctr CNIO, Human Genet Grp, Madrid, Spain, Spanish Natl Canc Ctr CNIO, Genotyping Unit, Madrid, Spain, Biomed Network Rare Dis CIBERER, Madrid, Spain, Ohio State Univ, Ctr Comprehens Canc, Div Human Genet, Dept Internal Med, Columbus, OH 43210 USA, Univ Calif San Francisco, Canc Risk Program, Helen Diller Family Canc Ctr, San Francisco, CA 94143 USA, Univ Quebec, Unite Rech Sante Populat, Ctr Malad Sein Deschenes Fabia, Ctr Rech FRSQ,Ctr Hosp, Quebec City, PQ, Canada, Latvian Biomed Res & Study Ctr, Riga, Latvia, Univ Penn, Philadelphia, PA 19104 USA, Landspitali Univ Hosp, Reykjavik, Iceland, Univ Iceland, Sch Med, Reykjavik, Iceland, Clalit Natl Israeli Canc Control Ctr, Haifa, Israel, Carmel Hosp, Dept Community Med & Epidemiol, Haifa, Israel, Peter MacCallum Canc Ctr, Familial Canc Ctr, Melbourne, Vic, Australia, Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden, Univ Cambridge, Ctr Canc Genet Epidemiol, Dept Oncol, Cambridge, England, McGill Univ, Dept Human Genet, Montreal, PQ, Canada, McGill Univ, Genome Quebec Innovat Ctr, Montreal, PQ, Canada

مصطلحات موضوعية: Brjóstakrabbamein, Erfðir, Gen, BRCA1 Protein, BRCA2 Protein, Breast Neoplasms, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Heterozygote, Humans, Middle Aged, Mutation, Ovarian Neoplasms, Polymorphism, Single Nucleotide, Prognosis, Risk Factors

العلاقة: http://dx.doi.org/10.1371/journal.pgen.1003212Test; PLoS Genet. 2013, 9 (3):e1003212; http://hdl.handle.net/2336/312762Test; PLoS genetics

الإتاحة: https://doi.org/10.1371/journal.pgen.1003212Test
http://hdl.handle.net/2336/312762Test

المؤلفون: Helgason, Hannes, Sulem, Patrick, Duvvari, Maheswara R, Luo, Hongrong, Thorleifsson, Gudmar, Stefansson, Hreinn, Jonsdottir, Ingileif, Masson, Gisli, Gudbjartsson, Daniel F, Walters, G Bragi, Magnusson, Olafur Th, Kong, Augustine, Rafnar, Thorunn, Kiemeney, Lambertus A, Schoenmaker-Koller, Frederieke E, Zhao, Ling, Boon, Camiel J F, Song, Yaojun, Fauser, Sascha, Pei, Michelle, Ristau, Tina, Patel, Shirrina, Liakopoulos, Sandra, van de Ven, Johannes P H, Hoyng, Carel B, Ferreyra, Henry, Duan, Yaou, Bernstein, Paul S, Geirsdottir, Asbjorg, Helgadottir, Gudleif, Stefansson, Einar, den Hollander, Anneke I, Zhang, Kang, Jonasson, Fridbert, Sigurdsson, Haraldur, Thorsteinsdottir, Unnur, Stefansson, Kari

المساهمون: deCODE Genet Amgen, Reykjavik, Iceland, Univ Iceland, Sch Engn & Nat Sci, Reykjavik, Iceland, Radboud Univ Nijmegen, Med Ctr, Dept Ophthalmol, NL-6525 ED Nijmegen, Netherlands, Univ Calif San Diego, Dept Ophthalmol, La Jolla, CA 92093 USA, Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA, Sichuan Univ, West China Hosp, Dept Ophthalmol, Chengdu 610064, Peoples R China, Sichuan Univ, West China Hosp, Mol Med Res Ctr, Chengdu 610064, Peoples R China, Natl Univ Hosp Reykjavik, Dept Immunol, Reykjavik, Iceland, Univ Iceland, Fac Med, Reykjavik, Iceland, Radboud Univ Nijmegen, Med Ctr, Dept Hlth Evidence, NL-6525 ED Nijmegen, Netherlands, Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6525 ED Nijmegen, Netherlands, Univ Hosp Cologne, Dept Ophthalmol, Cologne, Germany, Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA, Natl Univ Hosp Reykjavik, Dept Ophthalmol, Reykjavik, Iceland, Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6525 ED Nijmegen, Netherlands, Radboud Univ Nijmegen, Med Ctr, Inst Genet & Metab Dis, NL-6525 ED Nijmegen, Netherlands, Vet Affairs Healthcare Syst, San Diego, CA USA

مصطلحات موضوعية: Frumurannsóknir, Erfðir, Ísland, Amino Acid Substitution, Base Sequence, Complement Activation, Complement C3, Complement C3b, Complement Factor H, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Genotype, Humans, Iceland, Macular Degeneration, Polymorphism, Single Nucleotide, Risk, Sequence Analysis, DNA

العلاقة: http://dx.doi.org/10.1038/ng.2740Test; Nat. Genet. 2013, 45 (11):1371-4; http://hdl.handle.net/2336/313317Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.2740Test
http://hdl.handle.net/2336/313317Test

المؤلفون: Smoller, JW, Craddock, N, Kendler, K, Lee, PH, Neale, BM, Nurnberger, JI, Ripke, Stephan, Santangelo, S, Sullivan, PF, Psychiatric Genomics Consortium

المساهمون: Massachusetts Gen Hosp, Boston, MA 02114 USA

مصطلحات موضوعية: Þunglyndi, Skammdegisþunglyndi, ADHD, Geðklofi, Erfðir, Adult, Age of Onset, Attention Deficit Disorder with Hyperactivity, Bipolar Disorder, Calcium Channels, L-Type, Child, Child Development Disorders, Pervasive, Depressive Disorder, Major, Genetic Loci, Genome-Wide Association Study, Humans, Logistic Models, Polymorphism, Single Nucleotide, Schizophrenia

العلاقة: http://dx.doi.org/10.1016/S0140-6736Test(12)62129-1; Lancet 2013, 381 (9875):1371-9; http://hdl.handle.net/2336/312777Test; Lancet

الإتاحة: https://doi.org/10.1016/S0140-6736Test(12)62129-1
http://hdl.handle.net/2336/312777Test

المؤلفون: Dastani, Zari, Johnson, Toby, Kronenberg, Florian, Nelson, Christopher P, Assimes, Themistocles L, März, Winfried, Richards, J Brent

المساهمون: McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ H3T 1E2, Canada

مصطلحات موضوعية: Kransæðasjúkdómar, Æðakölkun, Gen, Erfðir, Adiponectin, Adiposity, Alleles, Atherosclerosis, Coronary Artery Disease, Databases, Genetic, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Prevalence, Risk Factors

العلاقة: http://dx.doi.org/10.1016/j.atherosclerosis.2013.03.034Test; Atherosclerosis 2013, 229 (1):145-8; http://hdl.handle.net/2336/312765Test; Atherosclerosis

الإتاحة: https://doi.org/10.1016/j.atherosclerosis.2013.03.034Test
http://hdl.handle.net/2336/312765Test

المؤلفون: Gunnar Sigurðsson, Vilmundur Guðnason

مصطلحات موضوعية: Erfðir, Blóðfita, Erfðafræði, Cholesterol

العلاقة: http://www.laeknabladid.isTest; Læknablaðið 1990, 76(2):81-92; http://hdl.handle.net/2336/98175Test; Læknablaðið

الإتاحة: http://hdl.handle.net/2336/98175Test

المؤلفون: Þorvaldur Ingvarsson, Halldór Baldursson

مصطلحات موضوعية: Slitgigt, Erfðir, Osteoarthritis, Hip, Rheumatic Diseases

العلاقة: http://www.laeknabladid.isTest; Læknablaðið 1991, 77(4):150-2; http://hdl.handle.net/2336/92354Test; Læknablaðið

الإتاحة: http://hdl.handle.net/2336/92354Test

المؤلفون: Engilbert Sigurðsson, Hreinn Stefánsson

مصطلحات موضوعية: Geðhvarfasýki, Erfðir, Geðsjúkdómar, Erfðafræði

العلاقة: Geðvernd 2005, 34(1):43-7; http://hdl.handle.net/2336/92321Test; Geðvernd

الإتاحة: http://hdl.handle.net/2336/92321Test

المؤلفون: Magnús Haraldsson, Hannes Pétursson

مصطلحات موضوعية: Geðsjúkdómar, Geðklofi, Erfðir, Schizophrenia

العلاقة: Geðvernd 2008, 37(1):41-5; http://hdl.handle.net/2336/91073Test; Geðvernd

الإتاحة: http://hdl.handle.net/2336/91073Test

المؤلفون: Davíð Gíslason

مصطلحات موضوعية: Asma, Erfðir, Reykingar, Ofnæmi, Öndunarfærasjúkdómar, Umhverfisáhrif, Loftmengun, Asthma, Hypersensitivity, Prevalence, Immediate

العلاقة: http://www.laeknabladid.isTest; Læknablaðið 1991, 77(9):349-56; http://hdl.handle.net/2336/87760Test; Læknablaðið

الإتاحة: http://hdl.handle.net/2336/87760Test

المؤلفون: Magnús Jóhannsson, Smári Pálsson, Jón Snædal, Pálmi V. Jónsson, Sigurbjörn Björnsson

مصطلحات موضوعية: Alzheimers-sjúkdómur, Heilabilun, Erfðir, Alzheimer Disease, Dementia

العلاقة: http://www.sal.isTest; Sálfræðiritið 2009, Fylgirit 1. 14:90-4; http://hdl.handle.net/2336/86716Test; Sálfræðiritið : Fylgirit

الإتاحة: http://hdl.handle.net/2336/86716Test