المؤلفون: Mitja Mitrovič, Nikolaos A Patsopoulos, Ashley H Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie B D'hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise W Thørner, Thomas Werge, Janna Saarela, Isabelle Cournu-Rebeix, Vincent Damotte, Bertrand Fontaine, Lena Guillot-Noel, Mark Lathrop, Sandra Vukusik, Pierre-Antoine Gourraud, Till F M Andlauer, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Antonios Bayas, Christoph Heesen, Tania Kümpfel, Ralf Linker, Friedemann Paul, Martin Stangel, Björn Tackenberg, Florian Then Bergh, Clemens Warnke, Heinz Wiendl, Brigitte Wildemann, Uwe Zettl, Ulf Ziemann, Hayrettin Tumani, Ralf Gold, Verena Grummel, Bernhard Hemmer, Benjamin Knier, Christina M Lill, Felix Luessi, Efthimios Dardiotis, Cristina Agliardi, Nadia Barizzone, Elisabetta Mascia, Luisa Bernardinelli, Giancarlo Comi, Daniele Cusi, Federica Esposito, Laura Ferrè, Cristoforo Comi, Daniela Galimberti, Maurizio A Leone, Melissa Sorosina, Julia Mescheriakova, Rogier Hintzen, Cornelia van Duijn, Charlotte E Teunissen, Steffan D Bos, Kjell-Morten Myhr, Elisabeth G Celius, Benedicte A Lie, Anne Spurkland, Manuel Comabella, Xavier Montalban, Lars Alfredsson, Pernilla Stridh, Jan Hillert, Maja Jagodic, Fredrik Piehl, Ilijas Jelčić, Roland Martin, Mireia Sospedra, Maria Ban, Clive Hawkins, Pirro Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Genevieve Lachance, Matthew Neville, Adam Santaniello, Stacy J Caillier, Peter A Calabresi, Bruce A C Cree, Anne Cross, Mary F Davis, Jonathan L Haines, Paul I W de Bakker, Silvia Delgado, Marieme Dembele, Keith Edwards, Kathryn C Fitzgerald, Hakon Hakonarson, Ioanna Konidari, Ellen Lathi, Clara P Manrique, Margaret A Pericak-Vance, Laura Piccio, Cathy Schaefer, Cristin McCabe, Howard Weiner, Jacqueline Goldstein, Tomas Olsson, Georgios Hadjigeorgiou, Bruce Taylor, Lotti Tajouri, Jac Charlesworth, David R Booth, Hanne F Harbo, Adrian J Ivinson, Stephen L Hauser, Alastair Compston, Graeme Stewart, Frauke Zipp, Lisa F Barcellos, Sergio E Baranzini, Filippo Martinelli-Boneschi, Sandra D'Alfonso, Andreas Ziegler, Annette Oturai, Jacob L McCauley, Stephen J Sawcer, Jorge R Oksenberg, Philip L De Jager, Ingrid Kockum, David A Hafler, Chris Cotsapas

المساهمون: M. Mitrovič, N. A Patsopoulo, A. H Beecham, T. Dankowski, A. Gori, B. Duboi, M. B D'hooghe, R. Lemmen, P. Van Damme, H. Bach Søndergaard, F. Sellebjerg, P. Soelberg Sorensen, H. Ullum, L. W Thørner, T. Werge, J. Saarela, I. Cournu-Rebeix, V. Damotte, B. Fontaine, L. Guillot-Noel, M. Lathrop, S. Vukusik, P. Gourraud, T.F. M Andlauer, V. Pongratz, D. Buck, C. Gasperi, A. Baya, C. Heesen, T. Kümpfel, R. Linker, F. Paul, M. Stangel, B. Tackenberg, F. Then Bergh, C. Warnke, H. Wiendl, B. Wildemann, U. Zettl, U. Ziemann, H. Tumani, R. Gold, V. Grummel, B. Hemmer, B. Knier, C. M Lill, F. Luessi, E. Dardioti, C. Agliardi, N. Barizzone, E. Mascia, L. Bernardinelli, G. Comi, D.M. Cusi, F. Esposito, L. Ferrè, C. Comi, D. Galimberti, M. A Leone, M. Sorosina, J. Mescheriakova, R. Hintzen, C. van Duijn, C. E Teunissen, S. D Bo, K. Myhr, E. G Celiu, B. A Lie, A. Spurkland, M. Comabella, X. Montalban, L. Alfredsson, P. Stridh, J. Hillert, M. Jagodic, F. Piehl, I. Jelčić, R. Martin, M. Sospedra, B. Maria, C. Hawkin, P. Hysi, S. Kalra, F. Karpe, J. Khadake, G. Lachance, M. Neville, A. Santaniello, S. J Caillier, P. A Calabresi, B.A. C Cree, A. Cro, M. F Davi, J. L Haine, P.I. W de Bakker, S. Delgado, M. Dembele, K. Edward, K. C Fitzgerald, H. Hakonarson

مصطلحات موضوعية: Case-Control Studie, Cell Cycle Protein, Chromosomes, Human, GTPase-Activating Protein, Gene Frequency, Genetic Loci, Genomic, Inheritance Pattern, Major Histocompatibility Complex, Microglia, Multiple Sclerosi, Polymorphism, Single Nucleotide, Quantitative Trait Loci, RNA-Seq, Transcriptome, Chromosome Mapping, Genome-Wide Association Study, Settore MED/26 - Neurologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/31604244; info:eu-repo/semantics/altIdentifier/wos/WOS:000488838600040; volume:365; issue:6460; firstpage:1417; journal:SCIENCE; http://hdl.handle.net/2434/744186; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85072692374

الاتاحة: http://hdl.handle.net/2434/744186
https://doi.org/10.1126/science.aav7188

المؤلفون: Sergio E. Baranzini, Pouya Khankhanian, Nikolaos A. Patsopoulos, Michael Li, Jim Stankovich, Chris Cotsapas, Helle Bach Søndergaard, Maria Ban, Nadia Barizzone, Laura Bergamaschi, David Booth, Dorothea Buck, Paola Cavalla, Elisabeth G. Celius, Manuel Comabella, Giancarlo Comi, Alastair Compston, Isabelle Cournu Rebeix, Sandra D’alfonso, Vincent Damotte, Lennox Din, Bénédicte Dubois, Irina Elovaara, Federica Esposito, Bertrand Fontaine, Andre Franke, An Goris, Pierre Antoine Gourraud, Christiane Graetz, Franca R. Guerini, Léna Guillot Noel, David Hafler, Hakon Hakonarson, Per Hall, Anders Hamsten, Hanne F. Harbo, Bernhard Hemmer, Jan Hillert, Anu Kemppinen, Ingrid Kockum, Keijo Koivisto, Malin Larsson, Mark Lathrop, Maurizio Leone, Christina M. Lill, Fabio Macciardi, Roland Martin, Vittorio Martinelli, Filippo Martinelli Boneschi, Jacob L. McCauley, Kjell Morten Myhr, Paola Naldi, Tomas Olsson, Annette Oturai, Margaret A. Pericak Vance, Franco Perla, Mauri Reunanen, Janna Saarela, Safa Saker Delye, SALVETTI, Marco, Finn Sellebjerg, Per Soelberg Sørensen, Anne Spurkland, Graeme Stewart, Bruce Taylor, Pentti Tienari, Juliane Winkelmann, Wellcome Trust Case Control Consortium 2 Frauke Zipp, Adrian J. Ivinson, Jonathan L. Haines, Stephen Sawcer, Philip DeJager, Stephen L. Hauser, Jorge R. Oksenberg

المساهمون: Sergio E., Baranzini, Pouya, Khankhanian, Nikolaos A., Patsopoulo, Michael, Li, Jim, Stankovich, Chris, Cotsapa, Helle Bach, Søndergaard, Maria, Ban, Nadia, Barizzone, Laura, Bergamaschi, David, Booth, Dorothea, Buck, Paola, Cavalla, Elisabeth G., Celiu, Manuel, Comabella, Giancarlo, Comi, Alastair, Compston, Isabelle Cournu, Rebeix, Sandra, D’Alfonso, Vincent, Damotte, Lennox, Din, Bénédicte, Duboi, Irina, Elovaara, Federica, Esposito, Bertrand, Fontaine, Andre, Franke, An, Gori, Pierre Antoine, Gourraud, Christiane, Graetz, Franca R., Guerini, Léna Guillot, Noel, David, Hafler, Hakon, Hakonarson, Per, Hall, Anders, Hamsten, Hanne F., Harbo, Bernhard, Hemmer, Jan, Hillert, Anu, Kemppinen, Ingrid, Kockum, Keijo, Koivisto, Malin, Larsson, Mark, Lathrop, Maurizio, Leone, Christina M., Lill, Fabio, Macciardi, Roland, Martin, Vittorio, Martinelli, Filippo Martinelli, Boneschi, Jacob L., Mccauley, Kjell Morten, Myhr, Paola, Naldi, Tomas, Olsson, Annette, Oturai, Margaret A., Pericak Vance, Franco, Perla, Mauri, Reunanen, Janna, Saarela, Safa Saker, Delye, Salvetti, Marco, Finn, Sellebjerg, Per Soelberg, Sørensen, Anne, Spurkland, Graeme, Stewart, Bruce, Taylor, Pentti, Tienari, Juliane, Winkelmann, Wellcome Trust Case Control Consortium, 2 Frauke Zipp, Adrian J., Ivinson, Jonathan L., Haine, Stephen, Sawcer, Philip, Dejager, Stephen L., Hauser, Jorge R., Oksenberg

مصطلحات موضوعية: network-based multiple sclerosis pathway, gwa, genome-wide association, disease genes

Relation: info:eu-repo/semantics/altIdentifier/pmid/23731539; info:eu-repo/semantics/altIdentifier/wos/WOS:000320415300003; volume:92; issue:6; firstpage:854; lastpage:865; numberofpages:12; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11573/559752; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84878883338

الاتاحة: http://hdl.handle.net/11573/559752
https://doi.org/10.1016/j.ajhg.2013.04.019

المؤلفون: Sudeshna eDas, Patricia G Mccaffrey, Megan eTalkington, Neil eAndrews, Stephane eCorlosquet, Adrian J Ivinson, Tim eClark

المصدر: Frontiers in Neuroinformatics, Vol 8 (2014)

مصطلحات موضوعية: Chronic Pain, Social Media, Semantic Web technologies, content management systems, Drupal, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://journal.frontiersin.org/Journal/10.3389/fninf.2014.00021/full; https://doaj.org/toc/1662-5196

URL الوصول: https://doaj.org/article/fbd19c604f9c4493aeeefe4b1a5157f9

المؤلفون: Giovanna Lalli, James Pickett, John Collinge, Tom Theys, Mathias Jucker, John Hardy, Peter van den Burg, Colin Smith, Dennis J. Selkoe, Stéphane Haïk, Guy M. Poppy, Adel Helmy, Charles Duyckaerts, Sheena E. Radford, Joost Schymkowitz, Seth Love, Giampietro Schiavo, Bart De Strooper, Zane Jaunmuktane, Veerle Compernolle, Robin Lemmens, I-Chun Lin, V. Hugh Perry, Richard Knight, Adrian J Ivinson, Henrik Zetterberg, Philippe Vandekerckhove, Simon Mead, Dietmar Rudolf Thal, Hans L. Zaaijer, Gustaf Edgren, Elsa Lauwers, Sebastian Brandner, Clare Walton, Pierre Tiberghien, Carol Routledge, Frederic Rousseau

المصدر: Lauwers, E, Lalli, G, Brandner, S, Collinge, J, Compernolle, V, Duyckaerts, C, Edgren, G, Haïk, S, Hardy, J, Helmy, A, Ivinson, A J, Jaunmuktane, Z, Jucker, M, Knight, R, Lemmens, R, Lin, I, Love, S, Mead, S, Perry, V H, Pickett, J, Poppy, G, Radford, S E, Rousseau, F, Routledge, C, Schiavo, G, Schymkowitz, J, Selkoe, D J, Smith, C, Thal, D R, Theys, T, Tiberghien, P, Van Den Burg, P, Vandekerckhove, P, Walton, C, Zaaijer, H L, Zetterberg, H & De Strooper, B 2020, ' Potential human transmission of amyloid β pathology: surveillance and risks ', Lancet Neurology, vol. 19, no. 10, pp. 872-878 . https://doi.org/10.1016/S1474-4422(20)30238-6
The lancet / Neurology 19(10), 872-878 (2020). doi:10.1016/S1474-4422(20)30238-6
Lauwers, E, Lalli, G, Brandner, S, Collinge, J, Compernolle, V, Duyckaerts, C, Edgren, G, Haik, S, Hardy, J, Helmy, A, Ivinson, A, Jaunmuktane, Z, Jucker, M, Knight, R, Lemmens, R, Love, S, Mead, S & de Strooper, B 2020, ' Potential human transmission of amyloid beta pathology : surveillance and risks ', Lancet Neurology, vol. 19, no. 10, pp. 872-878 . https://doi.org/10.1016/S1474-4422(20)30238-6

مصطلحات موضوعية: 0301 basic medicine, Pathology, Amyloid β, etiology [Alzheimer Disease], Disease, metabolism [Neurodegenerative Diseases], Creutzfeldt-Jakob Syndrome, etiology [Neurodegenerative Diseases], pathology [Alzheimer Disease], 0302 clinical medicine, Risk Factors, metabolism [Creutzfeldt-Jakob Syndrome], neurosurgery, Iatrogenic transmission, biology, Transmission (medicine), pathology [Neurodegenerative Diseases], Neurodegenerative Diseases, Parkinson Disease, Population Surveillance, transmission [Creutzfeldt-Jakob Syndrome], etiology [Parkinson Disease], Cerebral amyloid angiopathy, Amyloid-beta, metabolism [Alzheimer Disease], medicine.medical_specialty, Amyloid, Amyloid beta, metabolism [Parkinson Disease], metabolism [Amyloid beta-Peptides], blood transfusion, prion, 03 medical and health sciences, Alzheimer Disease, mental disorders, medicine, Dementia, Animals, Humans, ddc:610, proteopathic seed, pathology [Creutzfeldt-Jakob Syndrome], Amyloid beta-Peptides, iatrogenic transmission, business.industry, medicine.disease, toxicity [Amyloid beta-Peptides], pathology [Parkinson Disease], 030104 developmental biology, biology.protein, Neurology (clinical), business, 030217 neurology & neurosurgery

وصف الملف: application/pdf; Print-Electronic; application/vnd.openxmlformats-officedocument.wordprocessingml.document

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fbe9c29b01a6cad7e6359d854e24dfd
https://eprints.whiterose.ac.uk/161306/1/THELANCETNEUROLOGY-D-20-00204R3_Main_text_CLEAN.pdf

المؤلفون: Farren B.S. Briggs, Pierre Duquette, Roland G. Henry, Bernhard Hemmer, Lisa F. Barcellos, Efthimios Dardiotis, Aarno Palotie, Giancarlo Comi, Georgios M. Hadjigeorgiou, Bertrand Fontaine, Ashley Beecham, Adrian J. Ivinson, David A. Hafler, John W. McCauley, Tommy Olsson, Luisa Bernardinelli, Sergio E. Baranzini, Stephen Sawcer, Jun Ichi Kira, Elisabeth Gulowsen Celius, Rogier Q. Hintzen, Filippo Martinelli-Boneschi, Hanne F. Harbo, Katrina Dedham, Chris Cotsapas, Jonathan L. Haines, Christiane Gasperi, Seema Kalra, Xiaoming Jia, Felix Luessi, Noriko Isobe, Jorge R. Oksenberg, Till F. M. Andlauer, Clive Hawkins, Lohith Madireddy, Juliet Compston, Annette Bang Oturai, Bruce V. Taylor, Christina M. Lill, Kicheol Kim, Stephen L. Hauser, Olli Saarela, Bruce A.C. Cree, Francesco Esposito, Michael Khalil, Dana Horakova, Stacy J. Caillier, Nikolaos A. Patsopoulos, Roland Martin, Pierre-Antoine Gourraud, Manuel Comabella, Brian W. Kunkle, P. L. De Jager, Bénédicte Dubois, Steffan D. Bos, Matthew R Lincoln, Ingrid Kockum, An Goris, Sandra D'Alfonso, Tone Berge, Adam Santaniello, David R. Booth, Graeme J. Stewart, Frauke Zipp

المصدر: Nature communications, vol 10, iss 1
Nature Communications, Vol 10, Iss 1, Pp 1-2 (2019)

مصطلحات موضوعية: 0301 basic medicine, Cell specific, Multidisciplinary, Science, Systems biology, Multiple sclerosis, General Physics and Astronomy, 02 engineering and technology, General Chemistry, Computational biology, 021001 nanoscience & nanotechnology, medicine.disease, General Biochemistry, Genetics and Molecular Biology, Spelling, ddc, International Multiple Sclerosis Genetics Consortium, 03 medical and health sciences, 030104 developmental biology, medicine, lcsh:Q, 0210 nano-technology, Psychology, lcsh:Science, Gene

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e41a775b99b4ecbfe560e33d3cd923a
https://escholarship.org/uc/item/8dm3w4xj

المؤلفون: Fredrik Karpe, Graeme Stewart, Jan Hillert, Elisabetta Mascia, Matt J. Neville, Verena Grummel, Jonathan L. Haines, Kate Fitzgerald, Bernhard Hemmer, Julia Y Mescheriakova, Benedicte A. Lie, Efthimios Luessi, Federica Esposito, Andreas Ziegler, Ioanna Konidari, Cristin McCabe, Keith R. Edwards, Roland Martin, Daniele Cusi, Elisabeth Gulowsen Celius, Cristina Agliardi, Anne Spurkland, Georgios M. Hadjigeorgiou, Lena Guillot-Noel, Antonios Bayas, Uwe K. Zettl, Kjell-Morten Myhr, Maria Ban, Rogier Q. Hintzen, Frauke Zipp, Mireia Sospedra, Till F. M. Andlauer, Adrian J. Ivinson, Mary F. Davis, Mark Lathrop, Daniela Galimberti, Pierre-Antoine Gourraud, Genevieve Lachance, Bruce A.C. Cree, Robin Lemmens, Ashley Beecham, Steffan D. Bos, Bruce V. Taylor, Maurizio Leone, Manuel Comabella, Maja Jagodic, Helle Bach Søndergaard, David A. Hafler, Ingrid Kockum, Nadia Barizzone, Ralf Gold, Tania Kümpfel, Per Soelberg Sørensen, Seema Kalra, An Goris, Philip Van Damme, Marie B. D'hooghe, Cathy Schaefer, Efthimios Dardiotis, Alastair Compston, Lotti Tajoori, Sandra D'Alfonso, Ilijas Jelcic, Stephen Sawcer, Brigitte Wildemann, Friedemann Paul, Lise Wegner Thoerner, Silvia Delgado, Tomas Olsson, Mitja Mitrovic, Hayrettin Tumani, Henrik Ullum, Lisa F. Barcellos, Xavier Montalban, Ellen Lathi, Finn Sellebjerg, Thomas Werge, Christina M. Lill, Pernilla Stridh, Paul I.W. de Bakker, Cornelia M. van Duijn, Jyoti Khadake, Jac Charlesworth, Melissa Sorosina, Christiane Gasperi, Stephen L. Hauser, Anne H. Cross, Isabelle Cournu-Rebeix, Nikolaos A. Patsopoulos, Fredrik Piehl, Lars Alfredsson, Bertrand Fontaine, Marieme Dembele, Margaret A. Pericak-Vance, Janna Saarela, Ulf Ziemann, Annette Bang Oturai, Stacy J. Caillier, Jorge R. Oksenberg, Bénédicte Dubois, Björn Tackenberg, Christoph Heesen, Jacob L. McCauley, Florian Then Bergh, Clemens Warnke, Sergio E. Baranzini, Peter A. Calabresi, Chris Cotsapas, Clive Hawkins, Martin Stangel, Hakon Hakonarson, Sandra Vukusik, Christiane Graetz, Heinz Wiendl, Howard L. Weiner, Laura Piccio, Giancarlo Comi, Ralf A. Linker, Luisa Bernardinelli, Cristoforo Comi, Filippo Martinelli-Boneschi, Hanne F. Harbo, Dorothea Buck, Clara P. Manrique, David R. Booth, Benjamin Knier, Philip L. De Jager, Viola Pongratz, Laura Ferrè, Vincent Damotte, Adam Santaniello, Theresa Dankowski, Pirro G. Hysi

مصطلحات موضوعية: Genetics, 0303 health sciences, Linkage disequilibrium, Multiple sclerosis, Disease, Biology, Heritability, medicine.disease, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, medicine, Epistasis, Coding region, Gene, 030217 neurology & neurosurgery, 030304 developmental biology, Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca312b659a481d06422bdfe2f8ceb857

المؤلفون: Ana Trisini-Lipsanopoulos, Alice W. Flaherty, U. Shivraj Sohur, Shirley Eberly, John H. Growdon, Michael G. Schlossmacher, Karen Duong, Kaltra Dhima, Ira Shoulson, Michael T. Hayes, Bradley T. Hyman, Ken Marek, Dennis J. Selkoe, Michael A. Schwarzschild, Albert Y. Hung, Xianjun Dong, Joseph J. Locascio, Ganqiang Liu, Clemens R. Scherzer, Nicte I. Mejia, Adrian J. Ivinson, Anne-Marie Wills, Ashley N. Hoesing, Lewis Sudarsky, Bernard Ravina, Zhixiang Liao, Bin Zheng, David Oakes

المصدر: Brain. 138:2659-2671

مصطلحات موضوعية: Male, Parkinson's disease, Neuroimaging, Disease, Mitochondrion, Bioinformatics, Severity of Illness Index, Gene expression, medicine, Humans, Genetic Testing, RNA, Messenger, Cognitive decline, Radionuclide Imaging, Aged, Dopamine transporter, Dopamine Plasma Membrane Transport Proteins, biology, business.industry, Parkinson Disease, Odds ratio, Middle Aged, Microarray Analysis, medicine.disease, Gene Expression Regulation, Immunology, alpha-Synuclein, biology.protein, Biomarker (medicine), Female, Neurology (clinical), Cognition Disorders, business, Tropanes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d060ec2c25522ebe5b8850966374ef2d
https://doi.org/10.1093/brain/awv202

المؤلفون: Adrian J. Ivinson

المصدر: Neuron. 84(3):521-525

مصطلحات موضوعية: Cognitive science, Clinical Trials as Topic, Personal account, Mental Disorders, General Neuroscience, Neuroscience(all), Neurosciences, Variety (cybernetics), Unmet needs, Translational Research, Biomedical, Scale (social sciences), Humans, Cooperative Behavior, Nervous System Diseases, Element (criminal law), Psychology, Neuroscience, Translational neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e7d335ff78c17e3b5f675d04638cc49

المؤلفون: Bénédicte Dubois, Lucia Corrado, Deborah F. Mason, Allan G. Kermode, Pentti J. Tienari, Annette Bang Oturai, Charles Hillier, Adrian J. Ivinson, Stephen L. Hauser, Ashley Beecham, Jeannette Lechner-Scott, Vincent Thijs, Jonathan L. Haines, Sarah Edkins, Alexander T. Dilthey, Daniele Cusi, Guy Nagels, David A. Hafler, Mark Slee, Petra Nilsson, James S. Wiley, Lou Brundin, Amy Strange, Elizabeth Visser, Mireia Sospedra, Athena Hadjixenofontos, Sergio E. Baranzini, Jenny Link, Robert Andrews, Viola Biberacher, Helle Bach Søndergaard, Vittorio Martinelli, Tomas Olsson, Gillian L Hall, Stephen Sawcer, Stacy J. Caillier, Per Soelberg Sørensen, Céline Bellenguez, Cornelia M. van Duijn, Frauke Zipp, Nikolaos A. Patsopoulos, Cristin McCabe, Colin Freeman, Simon Broadley, Luisa Bernardinelli, Margaret A. Pericak-Vance, Jan Hillert, Wassila Carpentier, Sandip Shaunak, Anne Spurkland, Barnaby Fiddes, Judith Field, Jan Lycke, Christina M. Lill, Federica Esposito, Ioanna Konidari, Elisabeth Gulowsen Celius, Christian Gieger, Helmut Butzkueven, Ling Shen, James F. Wilson, Magdalena Lindén, Tejas S. Shah, Amie Baker, Dionysia K. Xifara, Hong Quach, Laura Bergamaschi, Rogier Q. Hintzen, Jacob L. McCauley, Janna Saarela, J W Thorpe, Christine Lebrun-Frenay, Felix Luessi, Sandra D'Alfonso, B. E. Kendall, Helga Westerlind, Giancarlo Comi, Nathalie Schnetz-Boutaud, Paola Brambilla, Chris Cotsapas, Anders Hamsten, William Camu, Achim Berthele, Kjell-Morten Myhr, Clive Hawkins, Richard Nicholas, James Harley, Carl A. Anderson, Keijo Koivisto, Irene Coman, Neil Robertson, Hakon Hakonarson, Finn Sellebjerg, Fredrik Piehl, Alessia Di Sapio, Loukas Moutsianas, Mehdi Alizadeh, Lars Alfredsson, Catherine Schaefer, David Rog, Virpi Leppa, C. Martin, Bruce A.C. Cree, Christopher Halfpenny, Irina Elovaara, Filippo Martinelli-Boneschi, Cordelia Langford, Hanne F. Harbo, Wim Robberecht, Isabelle Cournu-Rebeix, Steve Vucic, Izaura Lima Bomfim, Irene Y. Frohlich, Michelle Lee, Bertrand Fontaine, Bernhard Hemmer, Eva Zindler, Chris C. A. Spencer, Malin Larsson, Simon Shields, Ilijas Jelcic, Juliane Winkelmann, Jorge R. Oksenberg, Alastair Wilkins, Silvia Delgado, Volker Siffrin, Helena C. Kronsbein, Bruno Brochet, Panos Deloukas, Daniela Galimberti, Nikos Evangelou, Rebecca C. Selter, Maja Jagodic, Martin Duddy, Timothy Harrower, Per Hall, Nadia Barizzone, Siân Price, Matti Pirinen, Pierre-Antoine Gourraud, Thomas M.C. Binder, Giuseppe Liberatore, Mark Lathrop, M.-M. Hoshi, Garrett Hellenthal, Melissa Sorosina, Thomas Korn, Clara Guaschino, Roland Martin, Jeremy Hobart, Marco Salvetti, Peter Donnelly, Ingrid Kockum, An Goris, Alastair Compston, Mariaemma Rodegher, Dorothea Buck, Clara P. Manrique, Christiane Graetz, Benedicte A. Lie, Trevor J. Kilpatrick, Andrew Graham, Anu Kemppinen, Maria Ban, Gil McVean, John Zajicek, Hannah Blackburn, Mary F. Davis, Emilie Sundqvist, Bruce V. Taylor, Maurizio Leone, Lisa F. Barcellos, Fabio Macciardi, Gilles Defer, Vincent Damotte, Satu Männistö, Graeme J. Stewart, Gordon Mazibrada, Inger Lise Mero, Andre Franke, Philip L. De Jager, Verena Grummel, Mauri Reunanen, David R. Booth, Anna Ticca, Angela Jochim, Leentje Cosemans, Julia Y Mescheriakova, Cristina Agliardi, Paola Cavalla, Jeffrey C. Barrett, Sarah E. Hunt, Gavin Band

المساهمون: School of Life Sciences, University of Technology Sydney (UTS), Catholic University of Leuven - Katholieke Universiteit Leuven (KU Leuven), Profium Oy [Helsinki], Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institute of Clinical Medicine [Oslo], Faculty of Medicine [Oslo], University of Oslo (UiO)-University of Oslo (UiO), Michigan Technological University (MTU), The Wellcome Trust Centre for Human Genetics [Oxford], University of Oxford [Oxford], The Wellcome Trust Sanger Institute [Cambridge], Génétique épidémiologique et structures des populations humaines (Inserm U535), Epidémiologie, sciences sociales, santé publique (IFR 69), Université Paris 1 Panthéon-Sorbonne (UP1)-Université Paris-Sud - Paris 11 (UP11)-École des hautes études en sciences sociales (EHESS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris 1 Panthéon-Sorbonne (UP1)-Université Paris-Sud - Paris 11 (UP11)-École des hautes études en sciences sociales (EHESS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), UNIROUEN - UFR Santé (UNIROUEN UFR Santé), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU), Service de neurologie [Bordeaux], CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Karolinska Institutet [Stockholm], Institut des Neurosciences de Montpellier - Déficits sensoriels et moteurs (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Plateforme Post-génomique de la Pitié-Salpêtrière (P3S), UMS omique (OMIQUE), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Pierre et Marie Curie - Paris 6 - UFR de Médecine Pierre et Marie Curie (UPMC), Université Pierre et Marie Curie - Paris 6 (UPMC), Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CRICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de Neurologie [CHU Caen], Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Department of Statistics [Oxford], Centro Dino Ferrari [Milano], Università degli Studi di Milano [Milano] (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Epidémiologie et Analyses en Santé Publique : risques, maladies chroniques et handicap (LEASP), Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Medical Epidemiology and Biostatistics (MEB), University College of London [London] (UCL), Fondation Jean Dausset CEPH, Centre Hospitalier Universitaire de Nice (CHU Nice), Dublin Institute of Technology (DIT), University of California [Irvine] (UCI), University of California, Géosciences Environnement Toulouse (GET), Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Observatoire Midi-Pyrénées (OMP), Institut de Recherche pour le Développement (IRD)-Météo France-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Météo France-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS), Kaiser Permanente, Universität Zürich [Zürich] = University of Zurich (UZH), University Hospitals Leuven [Leuven], Department Biostatistics University of North Carolina, University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC)-University of North Carolina System (UNC), Institute of Bioinformatics and Systems Biology [München], Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Yale University School of Medicine, Big Data Institute, Department of Clinical Neurosciences [Cambridge], University of Cambridge [UK] (CAM), Faculty of Engineering, Neuroprotection & Neuromodulation, Internal Medicine Specializations, Neurology, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Centre National de la Recherche Scientifique (CNRS), Institut des Neurosciences de Montpellier (INM), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire Midi-Pyrénées (OMP), Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Université Fédérale Toulouse Midi-Pyrénées-Météo-France -Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Météo-France -Centre National de la Recherche Scientifique (CNRS), Yale School of Medicine [New Haven, Connecticut] (YSM), University of Oxford, Università degli Studi di Milano = University of Milan (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of California [Irvine] (UC Irvine), University of California (UC), Cardiology, Epidemiology, Oral and Maxillofacial Surgery, International Multiple Sclerosis Genetics, Consortium, Beecham, Ah, Patsopoulos, Na, Xifara, Dk, Davis, Mf, Kemppinen, A, Cotsapas, C, Shah, T, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli Boneschi, F, Taylor, B, Harbo, Hf, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, Jr, Hintzen, R, Barcellos, Lf, Wellcome Trust Case Control Consortium, 2, International IBD Genetics, Consortium, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, Hb, Baker, A, Band, G, Baranzini, Se, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, Tm, Blackburn, H, Bomfim, Il, Brambilla, P, Broadley, S, Brochet, B, Brundin, L, Buck, D, Butzkueven, H, Caillier, Sj, Camu, W, Carpentier, W, Cavalla, P, Celius, Eg, Coman, I, Comi, Giancarlo, Corrado, L, Cosemans, L, Cournu Rebeix, I, Cree, Ba, Cusi, D, Damotte, V, Defer, G, Delgado, Sr, Deloukas, P, di Sapio, A, Dilthey, At, Donnelly, P, Dubois, B, Duddy, M, Edkins, S, Elovaara, I, Esposito, F, Evangelou, N, Fiddes, B, Field, J, Franke, A, Freeman, C, Frohlich, Iy, Galimberti, D, Gieger, C, Gourraud, Pa, Graetz, C, Graham, A, Grummel, V, Guaschino, C, Hadjixenofontos, A, Hakonarson, H, Halfpenny, C, Hall, G, Hall, P, Hamsten, A, Harley, J, Harrower, T, Hawkins, C, Hellenthal, G, Hillier, C, Hobart, J, Hoshi, M, Hunt, Se, Jagodic, M, Jelčić, I, Jochim, A, Kendall, B, Kermode, A, Kilpatrick, T, Koivisto, K, Konidari, I, Korn, T, Kronsbein, H, Langford, C, Larsson, M, Lathrop, M, Lebrun Frenay, C, Lechner Scott, J, Lee, Mh, Leone, Ma, Leppä, V, Liberatore, G, Lie, Ba, Lill, Cm, Lindén, M, Link, J, Luessi, F, Lycke, J, Macciardi, F, Männistö, S, Manrique, Cp, Martin, R, Martinelli, V, Mason, D, Mazibrada, G, Mccabe, C, Mero, Il, Mescheriakova, J, Moutsianas, L, Myhr, Km, Nagels, G, Nicholas, R, Nilsson, P, Piehl, F, Pirinen, M, Price, Se, Quach, H, Reunanen, M, Robberecht, W, Robertson, Np, Rodegher, M, Rog, D, Salvetti, M, Schnetz Boutaud, Nc, Sellebjerg, F, Selter, Rc, Schaefer, C, Shaunak, S, Shen, L, Shields, S, Siffrin, V, Slee, M, Sorensen, P, Sorosina, M, Sospedra, M, Spurkland, A, Strange, A, Sundqvist, E, Thijs, V, Thorpe, J, Ticca, A, Tienari, P, van Duijn, C, Visser, Em, Vucic, S, Westerlind, H, Wiley, J, Wilkins, A, Wilson, Jf, Winkelmann, J, Zajicek, J, Zindler, E, Haines, Jl, Pericak Vance, Ma, Ivinson, Aj, Stewart, G, Hafler, D, Hauser, Sl, Compston, A, Mcvean, G, De Jager, P, Sawcer, Sj, Mccauley, J. L.

المصدر: Nature Genetics
Nature Genetics, Nature Publishing Group, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩
Beecham, A H, Patsopoulos, N A, Xifara, D K, Davis, M F, Kemppinen, A, Cotsapas, C, Shah, T S, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli-Boneschi, F, Taylor, B, Harbo, H F, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, J R, Hintzen, R, Barcellos, L F, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, H B, Baker, A, Band, G, Baranzini, S E, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, T M C, Blackburn, H, Bomfim, I L, Brambilla, P, Broadley, S, Wilson, J F & Henderson, P 2013, ' Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis ', Nature Genetics, vol. 45, no. 11, pp. 1353-60 . https://doi.org/10.1038/ng.2770
Nature genetics
Nature Genetics, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩
Nature Genetics, 45(11), 1353-+. Nature Publishing Group

مصطلحات موضوعية: Multiple Sclerosis, Genotype, [SDV]Life Sciences [q-bio], European Continental Ancestry Group, Genome-wide association study, CLEC16A, Biology, multiple sclerosis, Major histocompatibility complex, Polymorphism, Single Nucleotide, Article, White People, 03 medical and health sciences, 0302 clinical medicine, Research Support, N.I.H., Extramural, Gene Frequency, Polymorphism (computer science), Journal Article, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Genotyping, Allele frequency, 030304 developmental biology, 0303 health sciences, Research Support, Non-U.S. Gov't, Multiple sclerosis, Chromosome Mapping, Genetic Variation, medicine.disease, 3. Good health, Genetic Loci, biology.protein, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaed6c6a6596c74a380f29f543038e03
https://doi.org/10.1038/ng.2770

المؤلفون: Per Hall, Simon C. Potter, Richard Reynolds, Robert Heard, Gil McVean, An Goris, Joseph T. Glessner, Pamela Whittaker, Niall Tubridy, Olivier Gout, Ann-Christine Syvaenen, Leena Peltonen, Bénédicte Dubois, Anders Hamsten, Alastair Compston, Hugh S. Markus, Mariaemma Rodegher, Lisa F. Barcellos, Wendy Cozen, Rosetta M. Chiavacci, Jenefer M. Blackwell, William M. Carroll, Patricia P. Ramsay, Amie Baker, Krzysztof Selmaj, Serge Dronov, Zhan Su, C. Smestad, Stanley Hawkins, Janna Saarela, Matti Pirinen, Sabine Cepok, Gavin Band, Norman Klopp, Simon Heath, Sandra D'Alfonso, Peter Donnelly, Ina-Maria Rueckert, Deborah F. Mason, Alagurevathi Jayakumar, Hakon Hakonarson, Cecilia Kim, Colin Freeman, Jeannette Lechner-Scott, Marc Debouverie, Neil Robertson, Inger-Lise Mero, Paola Cavalla, Sabine Roesner, H-Erich Wichmann, Daniele Cusi, Wendy Ingram, Sarah Edkins, Tania Mihalova, Mark J. Daly, Mark Marriott, Roland Martin, Adrian J. Ivinson, Hong L. Quach, Jeremy Hobart, Filippo Martinelli Boneschi, Carmen Infante-Duarte, Catherine Schaefer, Irina Elovaara, Jonathan L. Haines, John Zajicek, Michelle Ricketts, Ananth C. Viswanathan, Colin A. Graham, Allan G. Kermode, Helmut Butzkueven, Kai Wang, John Mottershead, Francesca Taddeo, Stefan Schreiber, Aarno Palotie, Trevor Pickersgill, Naomi Hammond, David A. Hafler, Robert Plomin, Robin R. Lincoln, David Sexton, Jianjun Liu, Finn Sellebjerg, Françoise Clerget-Darpoux, David Brassat, Sarah E. Hunt, Per Soelberg Sørensen, Vittorio Martinelli, Eleni Giannoulatou, Paul I.W. de Bakker, Alexander T. Dilthey, Stephen Leslie, Ulrika Liljedahl, Hanne F. Harbo, Alison Page, Keijo Koivisto, Ingrid Kockum, Stephen L. Hauser, Ewa Tronczynska, Ayman Tourbah, K Baker, Panos Deloukas, Hannah Blackburn, Janusz Jankowski, Mauri Reunanen, Trevor J. Kilpatrick, Sheila Skidmore, Sergio E. Baranzini, Nicholas W. Wood, Fredrik Piehl, Lars Alfredsson, Daniela Galimberti, Federica Esposito, Marco Salvetti, Jennifer Liddle, Jenny Link, Helle Bach Søndergaard, Suzannah Bumpstead, Jonathan P. Bradfield, Richard C. Strange, Céline Bellenguez, David R. Booth, Refujia Gomez, Michael Wittig, Matthew A. Brown, Laura Bergamaschi, Elisabeth Gulowsen Celius, William E R Ollier, Juan P. Casas, Ling Shen, Loukas Moutsianas, Fabio Macciardi, Anne H. Cross, Maja Jagodic, Marie B. D'hooghe, Tomas Olsson, Mark D. Cossburn, O. T. McCann, Justin P. Rubio, Isabelle Cournu-Rebeix, Struan F.A. Grant, Colin N. A. Palmer, Matthew W. Gillman, John D. Rioux, Christopher G. Mathew, Maria Ban, Anna-Maija Sulonen, Garrett Hellenthal, Dorothea Buck, Jorge R. Oksenberg, Frauke Zipp, James Wason, Stephen Sawcer, Franca Rosa Guerini, Clive Hawkins, Cristin Aubin, Elvira Bramon, Paul A. Weston, Andre Franke, Laura Piccio, Jane Vickery, Nikolaos A. Patsopoulos, Jacob L. McCauley, Kristin G. Ardlie, A. Strange, Marcin P. Mycko, Richard C. Trembath, Giancarlo Comi, Gillian Ingram, Graeme J. Stewart, Allan L. Bernstein, Emilie Sundqvist, Xavier Montalban, Juliane Winkelmann, Rhian Gwilliam, Ruggero Capra, Bruce V. Taylor, Maurizio Leone, Brigid Simms-Acuna, Emma J. Davis, Bertrand Fontaine, Chris C. A. Spencer, Malin Larsson, Hans-Peter Hartung, Emma Gray, Virpi M. Leppä, Pablo Villoslada, Audrey Duncanson, Åslaug R. Lorentzen, Rathi Ravindrarajah, Izaura Lima Bomfim, Christian Schulze, Talat Islam, Manuel Comabella, Rita Dobosi, Simon Broadley, Bernhard Hemmer, Margaret A. Pericak-Vance, Jan Hillert, Michael Kabesch, J. Yaouanq, Mark Lathrop, Angelo Ghezzi, Rodney J. Scott, K Dixon, Jean Pelletier, Annette Bang Oturai, Mike Boggild, Philip L. De Jager, Anne Spurkland, M. Perez, Roby Abraham, Pentti J. Tienari, Matthew Waller, Katleen Clysters, Adam Santaniello, David Ellinghaus, Cordelia Langford, Anna Rautanen, Frank D. Mentch, Achim Berthele, Kjell-Morten Myhr, Simon J. Foote, Thomas M. Mack, Bruce A.C. Cree, Susan Pobywajlo, Ernest Willoughby, Haitao Zhang, M. B. Cox, Anu Kemppinen, Muna Hoshi, Sara Widaa, Claire Fontenille, Erika Salvi, Sara Lupoli, Aiden Corvin, Roberto Bergamaschi, Jim Stankovich, Rebecca L. Zuvich, Paola Naldi, Patrick M. A. Sleiman

المساهمون: Clinical sciences, Neuroprotection & Neuromodulation, Neurology, Faculty of Psychology and Educational Sciences

المصدر: Nature
Nature; Vol 476

مصطلحات موضوعية: Immunity, Cellular/genetics, Cellular immunity, Multiple Sclerosis, Genome-wide association study, CLEC16A, Biology, Polymorphism, Single Nucleotide, Cell Differentiation/immunology, Europe/ethnology, Major Histocompatibility Complex/genetics, Major Histocompatibility Complex, 03 medical and health sciences, 0302 clinical medicine, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, HLA-A Antigens/genetics, Alleles, 030304 developmental biology, Genetic association, Genetics, 0303 health sciences, Immunity, Cellular, Multidisciplinary, HLA-A Antigens, Genome, Human, Multiple sclerosis, Genetic Predisposition to Disease/genetics, HLA-DR Antigens/genetics, Lymphocyte differentiation, Cell Differentiation, HLA-DR Antigens, T-Lymphocytes, Helper-Inducer, RC346, medicine.disease, Polymorphism, Single Nucleotide/genetics, Genetic architecture, 3. Good health, Europe, Sample Size, Immunology, Genome, Human/genetics, Multiple Sclerosis/genetics, 030217 neurology & neurosurgery, T-Lymphocytes, Helper-Inducer/cytology, Genome-Wide Association Study, HLA-DRB1 Chains

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::108ffea600e6cbe168572c0258871510
https://doi.org/10.1038/nature10251

المؤلفون: Lisa F. Barcellos, Philip L. De Jager, William S. Bush, Ashley Beecham, Adrian J. Ivinson, David A. Hafler, Alastair Compston, Stephen Sawcer, Stephen L. Hauser, Rebecca L. Zuvich, Jonathan L. Haines, Margaret A. Pericak-Vance, Douglas P. Mortlock, Jacob L. McCauley

المصدر: Human Molecular Genetics. 20:3517-3524

مصطلحات موضوعية: Male, CCCTC-Binding Factor, Linkage disequilibrium, Multiple Sclerosis, Genotype, Monosaccharide Transport Proteins, Quantitative Trait Loci, Suppressor of Cytokine Signaling Proteins, Genome-wide association study, Single-nucleotide polymorphism, CLEC16A, Biology, Quantitative trait locus, Linkage Disequilibrium, Suppressor of Cytokine Signaling 1 Protein, Genetics, Humans, Genetic Predisposition to Disease, Lectins, C-Type, Molecular Biology, Gene, Genetics (clinical), Association Studies Articles, Chromosome, General Medicine, Repressor Proteins, Logistic Models, CTCF, Female, Chromosomes, Human, Pair 16, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21cea923a6006798def8ef840e33316e
https://doi.org/10.1093/hmg/ddr250

المؤلفون: Adrian J. Ivinson, Stephen L. Hauser, Jeannette Lechner-Scott, Franca Rosa Guerini, P. L. De Jager, R. Zuvich, David Sexton, Lisa F. Barcellos, Laura Bergamaschi, Anu Kemppinen, Jacob L. McCauley, Alastair Compston, Sandra D'Alfonso, Frank Dudbridge, Jonathan L. Haines, Margaret A. Pericak-Vance, Mathew B Cox, Neil Robertson, Amie Baker, James Wason, Maria Ban, Jorge R. Oksenberg, David A. Hafler, Stephen Sawcer

المصدر: Genes and immunity, vol 11, iss 8
Genes and immunity

مصطلحات موضوعية: Candidate gene, Membrane metalloendopeptidase like 1, Cell Cycle Proteins, Neurodegenerative, Linkage Disequilibrium, 0302 clinical medicine, 2.1 Biological and endogenous factors, genetics, Aetiology, Genetics (clinical), Genetics, 0303 health sciences, Chromosome Mapping, Single Nucleotide, MMEL1, Neprilysin, Kallikreins, Biotechnology, Adult, Multiple Sclerosis, Genotype, Immunology, Nerve Tissue Proteins, Locus (genetics), Single-nucleotide polymorphism, Biology, Autoimmune Disease, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Clinical Research, medicine, Humans, SNP, Genetic Predisposition to Disease, Polymorphism, 030304 developmental biology, Genetic association, Prevention, Multiple sclerosis, Human Genome, Neurosciences, Odds ratio, medicine.disease, Brain Disorders, Cytoskeletal Proteins, Case-Control Studies, ATP Citrate (pro-S)-Lyase, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a97eb7a131472f7bb8d906506ec811
https://doi.org/10.1038/gene.2010.36

المؤلفون: Christian Gieger, Federica Esposito, B. Bryneda, Per Soelberg Sørensen, Laura Bergamaschi, Elisabeth Gulowsen Celius, Ingrid Kockum, An Goris, Alastair Compston, Sandra D'Alfonso, Rodney J. Scott, P. I. W. de Bakker, Clive Hawkins, Barbara Elaine Stranger, Åslaug R. Lorentzen, Paola Cavalla, Annette Bang Oturai, Anne Spurkland, Janna Saarela, Helle Bach Søndergaard, Jeannette Lechner-Scott, Jacob L. McCauley, Adrian J. Ivinson, Filippo Martinelli Boneschi, Lars Alfredsson, Tomas Olsson, Carmen Infante-Duarte, Jonathan L. Haines, Sabine Cepok, Aarno Palotie, Lisa F. Barcellos, Stephen L. Hauser, Robert Heard, Manuel Comabella, Frauke Zipp, Leena Peltonen, Bénédicte Dubois, Rita Dobosi, Mauri Reunanen, John D. Rioux, Jorge R. Oksenberg, Juliane Winkelmann, Virpi M. Leppä, Maurizio Leone, Keijo Koivisto, P. L. De Jager, Margaret A. Pericak-Vance, Jan Hillert, Roberto Bergamaschi, Cristin Aubin, David A. Hafler, Inger-Lise Mero, Bruce A.C. Cree, Neil Robertson, Stephen Sawcer, Finn Sellebjerg, William S. Bush, Isabelle Cournu-Rebeix, Hanne F. Harbo, B. Hemmer, Luisa Bernardinelli, Gary W. Beecham, Mathew B Cox, David R. Booth, Graeme J. Stewart, Nikolaos A. Patsopoulos, Mark J. Daly, G. Comi, Bertrand Fontaine

المصدر: Genes & Immunity. 11:397-405

مصطلحات موضوعية: Multiple Sclerosis, Immunology, Genome-wide association study, Locus (genetics), Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, Interleukin-12 Subunit p35, Cell Line, 03 medical and health sciences, 0302 clinical medicine, IL12A, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Genetics (clinical), Cell Proliferation, 030304 developmental biology, 0303 health sciences, Tumor Suppressor Proteins, Multiple sclerosis, Cell cycle, medicine.disease, 3. Good health, Celiac Disease, Case-Control Studies, Expression quantitative trait loci, Leukocytes, Mononuclear, RGS Proteins, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7990f1aa1af4deaac9d8ce8c6956ca1e
https://doi.org/10.1038/gene.2010.28

المؤلفون: Jacob L. McCauley, Ashley Beecham, David A. Hafler, John D. Rioux, Maria Ban, Jorge R. Oksenberg, Jonathan L. Haines, Adrian J. Ivinson, Stephen Sawcer, Neelum T. Aggarwal, Denis A. Evans, Laura Piccio, Susan Pobywajlo, Anne H. Cross, Lisa F. Barcellos, Ioanna Konidari, Bruce A.C. Cree, Stephen L. Hauser, Patrice L. Whitehead, Wendy L. McArdle, Margaret A. Pericak-Vance, Susan Romano, Cristin Aubin, Rebeccah Briskin, Rebecca L. Zuvich, Alastair Compston, David P. Strachan, Philip L. De Jager

المصدر: Human Molecular Genetics

مصطلحات موضوعية: Multiple Sclerosis, Genotype, Kinesins, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, SNP, Molecular Biology, Genetics (clinical), 030304 developmental biology, Genetic association, 0303 health sciences, Genome, Human, Multiple sclerosis, Association Studies Articles, Case-control study, Membrane Proteins, General Medicine, Odds ratio, medicine.disease, 3. Good health, Case-Control Studies, Human genome, Disease Susceptibility, 030217 neurology & neurosurgery, Follow-Up Studies, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8acedf3b1261c90127ef7813684c2b03
https://doi.org/10.1093/hmg/ddp542

المؤلفون: Ammar Al-Chalabi, Ting Jan Cho, Thomas J. Kwiatkowski, Michael A. van Es, Hylke M. Blauw, H. Robert Horvitz, Christopher Shaw, Alayna Barnes-Nessa, Peter C. Sapp, Nicole R. Couture, Christiaan G J Saris, Roel A. Ophoff, Philippe Corcia, Betsy A. Hosler, Lijia Shi, Vincenzo Silani, Aslihan Ozoguz, Adrian J. Ivinson, François Salachas, Pilar Galan, Valerie K. Hansen, Robert H. Brown, John Powell, Orla Hardiman, Claire L. Simpson, Jonathan D. Glass, Diane McKenna-Yasek, Shaun Purcell, John Landers, Jan H. Veldink, Simon Cronin, Franck Georges, Nicola Ticozzi, P. Nigel Leigh, Paul W.J. van Vught, Vincent Meininger, John H. J. Wokke, Wendy J. Broom, Meraida Polak, Mark Lathrop, Simon Heath, Anne-Marie Wills, Ildefonso Rodriguez-Leyva, Leonard H. van den Berg, Frank P. Diekstra, Judith Melki

المصدر: Proceedings of the National Academy of Sciences. 106:9004-9009

مصطلحات موضوعية: Genetics, Linkage disequilibrium, Multidisciplinary, Amyotrophic Lateral Sclerosis, Single-nucleotide polymorphism, Genome-wide association study, Biological Sciences, Biology, medicine.disease, Polymorphism, Single Nucleotide, Cytoskeletal Proteins, KIFAP3, medicine, Humans, SNP, Allele, Amyotrophic lateral sclerosis, Promoter Regions, Genetic, Alleles, Adaptor Proteins, Signal Transducing, SNP array

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761d58ebcc4be4e37ec5fd3a44ea5c35
https://doi.org/10.1073/pnas.0812937106

المؤلفون: Richard C. Strange, Maria Ban, Jorge R. Oksenberg, Elisabeth Gulowsen Celius, Lisa F. Barcellos, Hanne F. Harbo, Graeme J. Stewart, Tomas Olsson, Jenny Link, Robert Heard, An Goris, David A. Hafler, Philip L. De Jager, David Sexton, Stephen Sawcer, Margaret A. Pericak-Vance, Jan Hillert, Clive Hawkins, Tania Mihalova, Bénédicte Dubois, Åslaug R. Lorentzen, Alastair Compston, Jacob L. McCauley, Neil Robertson, David R. Booth, Ingrid Kockum, Anne Spurkland, Stephen L. Hauser, Adrian J. Ivinson, Rita Dobosi, Amie Baker, Jonathan L. Haines, Gillian Ingram

المصدر: Genes & Immunity. 10:11-14

مصطلحات موضوعية: Adult, Antigens, Differentiation, T-Lymphocyte, Multiple Sclerosis, Monosaccharide Transport Proteins, CD226, Immunology, Single-nucleotide polymorphism, CLEC16A, Immunogenetics, Biology, medicine.disease_cause, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Article, Autoimmunity, Belgium, Confidence Intervals, Odds Ratio, Genetics, medicine, Humans, Family, Genetic Predisposition to Disease, Lectins, C-Type, Gene, Alleles, Genetics (clinical), Adaptor Proteins, Signal Transducing, Probability, Sweden, Autoimmune disease, Norway, Multiple sclerosis, Australia, Tryptophan, Middle Aged, medicine.disease, United Kingdom, United States, Diabetes Mellitus, Type 1, Amino Acid Substitution, Case-Control Studies

وصف الملف: Print-Electronic; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d24a0baa8af398e52a6e84d3c2c836
https://doi.org/10.1038/gene.2008.83

المؤلفون: Roger Lane, Eric Siemers, Patrick C. May, Adrian J. Ivinson, Maria C. Carrillo, David A. Hosford

المصدر: Alzheimer's & Dementia. 4:80-88

مصطلحات موضوعية: medicine.medical_specialty, Drug Industry, Epidemiology, Alternative medicine, Disease, Pharmacology, Cellular and Molecular Neuroscience, Developmental Neuroscience, Alzheimer Disease, Basic research, medicine, Animals, Humans, health care economics and organizations, Pharmaceutical industry, Academic Medical Centers, Clinical Trials as Topic, Drug discovery, business.industry, Health Policy, Public relations, Psychiatry and Mental health, Interinstitutional Relations, Drug development, Drug Design, General partnership, Neurology (clinical), Geriatrics and Gerontology, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d1055e8b88ac4bce0cce3a5523a36b
https://doi.org/10.1016/j.jalz.2008.02.004

المؤلفون: Lisa F. Barcellos, Adrian J. Ivinson, David A. Hafler, An Goris, Amie Walton, Emily Walsh, Alastair Compston, Mark J. Daly, Stephen Sawcer, Stephan Beck, Todd Green, John D. Rioux, Maria Ban, Jorge R. Oksenberg, Chiara Fenoglio, Margaret A. Pericak-Vance, Jonathan L. Haines, Cara S Wolfish, Simon G. Gregory, Tai Wai Yeo, Craig J. Taylor, James A. Traherne, John Trowsdale, Stephen L. Hauser, Philip L. De Jager, Eric S. Lander, Reyna S. Goodman, Stacy J. Caillier, Susan Pobywajlo, Roger Horton

المصدر: Annals of Neurology
Annals of neurology, vol 61, iss 3

مصطلحات موضوعية: Adult, Male, Linkage disequilibrium, Multiple Sclerosis, Population, Clinical Sciences, Single-nucleotide polymorphism, Locus (genetics), Human leukocyte antigen, Biology, Neurodegenerative, Autoimmune Disease, Polymorphism, Single Nucleotide, Major Histocompatibility Complex, 03 medical and health sciences, 0302 clinical medicine, Genetics, 2.1 Biological and endogenous factors, Humans, Genetic Predisposition to Disease, Allele, Polymorphism, Aetiology, 10. No inequality, education, 030304 developmental biology, 0303 health sciences, education.field_of_study, HLA-D Antigens, Neurology & Neurosurgery, Inflammatory and immune system, Haplotype, Human Genome, Neurosciences, Single Nucleotide, Middle Aged, Brain Disorders, Neurology, Allelic heterogeneity, Original Article, Female, Neurology (clinical), 030215 immunology, Microsatellite Repeats

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::993daf124c0b610378c92aab48953d1c
http://europepmc.org/articles/PMC2737610

المؤلفون: Nikolaos A. Patsopoulos, Gil McVean, Juliane Winkelmann, F. Martinelli-Boneschi, An Goris, A Compston, Gourraud P-A., Hanne F. Harbo, Calliope A. Dendrou, Annette Bang Oturai, Elisabeth Gulowsen Celius, Dionysia Kiara Xifara, Sandra D'Alfonso, B. Hemmer, Lars Fugger, Helle Bach Søndergaard, Peter Donnelly, Luke Jostins, Sergio E. Baranzini, Frauke Zipp, Binder Tmc., Tomas Olsson, Lars Alfredsson, Ashley Beecham, Carl A. Anderson, Bénédicte Dubois, David A. Hafler, Janna Saarela, Maria Ban, Jorge R. Oksenberg, Ingrid Kockum, Margaret A. Pericak-Vance, Jan Hillert, Jacob L. McCauley, Stephen Sawcer, Kathrine E. Attfield, Bertrand Fontaine, Chris Cotsapas, Christiane Graetz, P. L. De Jager, Christina M. Lill, Bruce V. Taylor, Stephen Leslie, Jonathan L. Haines, Dorothea Buck, Stephen L. Hauser, Anne Spurkland, Jeffrey C. Barrett, Tejas Shah, Spencer Cca., David R. Booth, Loukas Moutsianas, Adrian J. Ivinson, Alexander T. Dilthey, Graeme J. Stewart

مصطلحات موضوعية: Genetics, musculoskeletal diseases, Multiple Sclerosis, Histocompatibility Antigens Class II, Single-nucleotide polymorphism, Genome-wide association study, Epistasis, Genetic, Human leukocyte antigen, Biology, Polymorphism, Single Nucleotide, Article, Histocompatibility, Genetic variation, Humans, Genetic Predisposition to Disease, Allele, 10. No inequality, HLA-DRB1, Alleles, Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e383fdaa0fd14fba880840f06454b89
https://europepmc.org/articles/PMC4874245/

المؤلفون: L. Moutsianas, L. Jostins, A. H. Beecham, A. T. Dilthey, D. K. Xifara, M. Ban, T. S. Shah, N. A. Patsopoulos, L. Alfredsson, C. A. Anderson, K. E. Attfield, S. E. Baranzini, J. Barrett, T. M. C. Binder, D. Booth, D. Buck, E. G. Celius, C. Cotsapas, S. D'Alfonso, C. A. Dendrou, P. Donnelly, B. Dubois, B. Fontaine, L. Fugger, A. Goris, P. Gourraud, C. Graetz, B. Hemmer, J. Hillert, I. Kockum, S. Leslie, C. M. Lill, J. R. Oksenberg, T. Olsson, A. Oturai, J. Saarela, H. B. Søndergaard, A. Spurkland, B. Taylor, J. Winkelmann, F. Zipp, J. L. Haines, M. A. Pericak Vance, C. C. A. Spencer, G. Stewart, D. A. Hafler, A. J. Ivinson, H. F. Harbo, S. L. Hauser, P. L. De Jager, A. Compston, J. L. Mccauley, S. Sawcer, G. Mcvean, F. Martinelli-Boneschi

المساهمون: L. Moutsiana, L. Jostin, A.H. Beecham, A.T. Dilthey, D.K. Xifara, M. Ban, T.S. Shah, N.A. Patsopoulo, L. Alfredsson, C.A. Anderson, K.E. Attfield, S.E. Baranzini, J. Barrett, T.M.C. Binder, D. Booth, D. Buck, E.G. Celiu, C. Cotsapa, S. D'Alfonso, C.A. Dendrou, P. Donnelly, B. Duboi, B. Fontaine, L. Fugger, A. Gori, P. Gourraud, C. Graetz, B. Hemmer, J. Hillert, I. Kockum, S. Leslie, C.M. Lill, F. Martinelli-Boneschi, J.R. Oksenberg, T. Olsson, A. Oturai, J. Saarela, H.B. Søndergaard, A. Spurkland, B. Taylor, J. Winkelmann, F. Zipp, J. L Haine, M.A. Pericak-Vance, C.C.A. Spencer, G. Stewart, D.A. Hafler, A.J. Ivinson, H.F. Harbo, S.L. Hauser, P.L. De Jager, A. Compston, J.L. Mccauley, S. Sawcer, G. Mcvean

مصطلحات موضوعية: Allele, Epistasis, Genetic, Histocompatibility Antigens Class II, Human, Multiple Sclerosi, Polymorphism, Single Nucleotide, Genetic Predisposition to Disease, Genetics, Settore MED/26 - Neurologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/26343388; info:eu-repo/semantics/altIdentifier/wos/WOS:000361969900005; volume:47; issue:10; firstpage:1107; lastpage:1113; numberofpages:7; journal:NATURE GENETICS; http://hdl.handle.net/2434/516079; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84942981489

الاتاحة: http://hdl.handle.net/2434/516079
https://doi.org/10.1038/ng.3395