المؤلفون: International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David

المصدر: Nature. 476(7359)

مصطلحات موضوعية: International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, T-Lymphocytes, Helper-Inducer, Humans, Multiple Sclerosis, Genetic Predisposition to Disease, HLA-A Antigens, HLA-DR Antigens, Sample Size, Cell Differentiation, Immunity, Cellular, Major Histocompatibility Complex, Polymorphism, Single Nucleotide, Alleles, Genome, Human, Europe, Genome-Wide Association Study, HLA-DRB1 Chains, Genetics, Neurosciences, Neurodegenerative, Clinical Research, Brain Disorders, Autoimmune Disease, Human Genome, 2.1 Biological and endogenous factors, Neurological, Inflammatory and immune system, General Science & Technology

الوصول الحر: https://escholarship.org/uc/item/5x17t6tzTest

المؤلفون: Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Celine, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Boneschi, Filippo Martinelli, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Francoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Benedicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica

المصدر: Nature. 476(7359)

مصطلحات موضوعية: Neurosciences, Prevention, Multiple Sclerosis, Biotechnology, Autoimmune Disease, Genetics, Brain Disorders, Human Genome, Neurodegenerative, 2.1 Biological and endogenous factors, Aetiology, Neurological, Inflammatory and immune system, Alleles, Cell Differentiation, Europe, Genetic Predisposition to Disease, Genome, Human, Genome-Wide Association Study, HLA-A Antigens, HLA-DR Antigens, HLA-DRB1 Chains, Humans, Immunity, Cellular, Major Histocompatibility Complex, Polymorphism, Single Nucleotide, Sample Size, T-Lymphocytes, Helper-Inducer, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, General Science & Technology

الوصول الحر: https://escholarship.org/uc/item/5x17t6tzTest

المؤلفون: Søndergaard, Helle Bach, Petersen, Eva Rosa, Magyari, Melinda, Sellebjerg, Finn, Oturai, Annette Bang

المصدر: Søndergaard , H B , Petersen , E R , Magyari , M , Sellebjerg , F & Oturai , A B 2017 , ' Genetic burden of MS risk variants distinguish patients from healthy individuals but are not associated with disease activity ' , Multiple Sclerosis and Related Disorders , vol. 13 , pp. 25-27 . https://doi.org/10.1016/j.msard.2017.01.015Test

مصطلحات موضوعية: Adult, Alleles, Female, Genetic Predisposition to Disease, HLA Antigens/genetics, Humans, Interferon-beta/therapeutic use, Male, Multiple Sclerosis/drug therapy, Polymorphism, Single Nucleotide, Risk Factors

الإتاحة: https://doi.org/10.1016/j.msard.2017.01.015Test
https://curis.ku.dk/portal/da/publications/genetic-burden-of-ms-risk-variants-distinguish-patients-from-healthy-individuals-but-are-not-associated-with-disease-activityTest(4ec44517-1653-443f-bc81-9ac67b09b58d).html

المؤلفون: F. Martinelli-Boneschi, Esposito, Federica, Brambilla, Paola, Lindström, Eva, Lavorgna, Giovanni, Stankovich, Jim, Rodegher, Mariaemma, Capra, Ruggero, Ghezzi, Angelo, Coniglio, Gabriella, Colombo, Bruno, Sorosina, Melissa, Martinelli, Vittorio, Booth, David, Oturai, Annette Bang, Stewart, Graeme, Harbo, Hanne F., Kilpatrick, Trevor John, Hillert, Jan, Rubio, Justin P., Abderrahim, Hadi, Wojcik, Jerome, Comi, Giancarlo

المساهمون: F. Martinelli-Boneschi, F. Esposito, P. Brambilla, E. Lindstrã¶m, G. Lavorgna, J. Stankovich, M. Rodegher, R. Capra, A. Ghezzi, G. Coniglio, B. Colombo, M. Sorosina, V. Martinelli, D. Booth, A.B. Oturai, G. Stewart, H.F. Harbo, T.J. Kilpatrick, J. Hillert, J.P. Rubio, H. Abderrahim, J. Wojcik, G. Comi

مصطلحات موضوعية: association studies in genetic, genome-wide association study, multiple sclerosi, primary progressive, single nucleotide polymorphism, Chromosomes, Human, Pair 7, Female, Genetic Predisposition to Disease, Genotype, HLA Antigen, Linkage Disequilibrium, Male, Middle Aged, Multiple Sclerosis, Chronic Progressive, Polymorphism, Single Nucleotide, Neurology, Neurology (clinical), Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22457343; info:eu-repo/semantics/altIdentifier/pmid/000309359000006; info:eu-repo/semantics/altIdentifier/wos/WOS:000309359000006; volume:18; issue:10; firstpage:1384; lastpage:1394; numberofpages:11; journal:MULTIPLE SCLEROSIS; http://hdl.handle.net/2434/533445Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84867011935

الإتاحة: https://doi.org/10.1177/1352458512439118Test
http://hdl.handle.net/2434/533445Test