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by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M.C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A.C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and Di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and Wellcome Trust Case Control Consor and Int IBD Genetics Consortium IIBDGC and International Multiple Sclerosis Genetics Consortium (IMSGC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International IBD Genetics Consortium (IIBDGC) and Institutionen för fysik, kemi och biologi and Linköpings universitet and Bioinformatik and Tekniska högskolan
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 11, pp. 1353 - 1362
Journal Article
by Sawcer, Stephen and Hellenthal, Garrett and Pirinen, Matti and Spencer, Chris C.A and Patsopoulos, Nikolaos A and Moutsianas, Loukas and Dilthey, Alexander and Su, Zhan and Freeman, Colin and Hunt, Sarah E and Edkins, Sarah and Gray, Emma and Booth, David R and Potter, Simon C and Goris, An and Band, Gavin and Oturai, Annette Bang and Strange, Amy and Saarela, Janna and Bellenguez, Céline and Fontaine, Bertrand and Gillman, Matthew and Hemmer, Bernhard and Gwilliam, Rhian and Zipp, Frauke and Jayakumar, Alagurevathi and Martin, Roland and Leslie, Stephen and Hawkins, Stanley and Giannoulatou, Eleni and D'Alfonso, Sandra and Blackburn, Hannah and Boneschi, Filippo Martinelli and Liddle, Jennifer and Harbo, Hanne F and Perez, Marc L and Spurkland, Anne and Waller, Matthew J and Mycko, Marcin P and Ricketts, Michelle and Comabella, Manuel and Hammond, Naomi and Kockum, Ingrid and McCann, Owen T and Ban, Maria and Whittaker, Pamela and Kemppinen, Anu and Weston, Paul and Hawkins, Clive and Widaa, Sara and Zajicek, John and Dronov, Serge and Robertson, Neil and Bumpstead, Suzannah J and Barcellos, Lisa F and Ravindrarajah, Rathi and Abraham, Roby and Alfredsson, Lars and Ardlie, Kristin and Aubin, Cristin and Baker, Amie and Baker, Katharine and Baranzini, Sergio E and Bergamaschi, Laura and Bergamaschi, Roberto and Bernstein, Allan and Berthele, Achim and Boggild, Mike and Bradfield, Jonathan P and Brassat, David and Broadley, Simon A and Buck, Dorothea and Butzkueven, Helmut and Capra, Ruggero and Carroll, William M and Cavalla, Paola and Celius, Elisabeth G and Cepok, Sabine and Chiavacci, Rosetta and Clerget-Darpoux, Françoise and Clysters, Katleen and Comi, Giancarlo and Cossburn, Mark and Cournu-Rebeix, Isabelle and Cox, Mathew B and Cozen, Wendy and Cree, Bruce A.C and Cross, Anne H and Cusi, Daniele and Daly, Mark J and Davis, Emma and De Bakker, Paul I.W and Debouverie, Marc and D'Hooghe, Marie Beatrice and Dixon, Katherine and Dobosi, Rita and Dubois, Bénédicte and Ellinghaus, David and Elovaara, Irina and Esposito, Federica and ... and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7359, pp. 214 - 219
Journal Article
by Mitrovič, Mitja and Patsopoulos, Nikolaos A and Beecham, Ashley H and Dankowski, Theresa and Goris, An and Dubois, Bénédicte and D’hooghe, Marie B and Lemmens, Robin and Van Damme, Philip and Søndergaard, Helle Bach and Sellebjerg, Finn and Sorensen, Per Soelberg and Ullum, Henrik and Thørner, Lise W and Werge, Thomas and Saarela, Janna and Cournu-Rebeix, Isabelle and Damotte, Vincent and Fontaine, Bertrand and Guillot-Noel, Lena and Lathrop, Mark and Vukusik, Sandra and Gourraud, Pierre-Antoine and Andlauer, Till F.M and Pongratz, Viola and Buck, Dorothea and Gasperi, Christiane and Bayas, Antonios and Heesen, Christoph and Kümpfel, Tania and Linker, Ralf and Paul, Friedemann and Stangel, Martin and Tackenberg, Björn and Bergh, Florian Then and Warnke, Clemens and Wiendl, Heinz and Wildemann, Brigitte and Zettl, Uwe and Ziemann, Ulf and Tumani, Hayrettin and Gold, Ralf and Grummel, Verena and Hemmer, Bernhard and Knier, Benjamin and Lill, Christina M and Luessi, Felix and Dardiotis, Efthimios and Agliardi, Cristina and Barizzone, Nadia and Mascia, Elisabetta and Bernardinelli, Luisa and Comi, Giancarlo and Comi, Cristoforo and Cusi, Daniele and Esposito, Federica and Ferrè, Laura and Galimberti, Daniela and Leone, Maurizio A and Sorosina, Melissa and Mescheriakova, Julia and Hintzen, Rogier and van Duijn, Cornelia and Theunissen, Charlotte E and Bos, Steffan D and Myhr, Kjell-Morten and Celius, Elisabeth G and Lie, Benedicte A and Spurkland, Anne and Comabella, Manuel and Montalban, Xavier and Alfredsson, Lars and Stridh, Pernilla and Hillert, Jan and Jagodic, Maja and Piehl, Fredrik and Jelčić, Ilijas and Martin, Roland and Sospedra, Mireia and Ban, Maria and Hawkins, Clive and Hysi, Pirro and Kalra, Seema and Karpe, Fredrik and Khadake, Jyoti and Lachance, Genevieve and Neville, Matthew and Santaniello, Adam and Caillier, Stacy J and Calabresi, Peter A and Cree, Bruce A.C and Cross, Anne and Davis, Mary F and Haines, Jonathan L and de Bakker, Paul I.W and Delgado, Silvia and Dembele, Marieme and Edwards, Keith and Fitzgerald, Kathryn C and Hakonarson, Hakon and ... and Int Multiple Sclerosis Genetics and International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu and International Multiple Sclerosis Genetics Consortium
Cell, ISSN 0092-8674, 11/2018, Volume 175, Issue 6, pp. 1679 - 1687.e7
Multiple sclerosis is a complex neurological disease, with ∼20% of risk heritability attributable to common genetic variants, including >230 identified by... 
Journal Article
by Patsopoulos, NA and Baranzini, SE and Santaniello, A and Shoostari, P and Cotsapas, C and Wong, G and Beecham, AH and James, T and Replogle, J and Vlachos, IS and McCabe, C and Pers, TH and Brandes, A and White, C and Keenan, B and Cimpean, M and Winn, P and Panteliadis, IP and Robbins, A and Andlauer, TFM and Zarzycki, O and Dubois, B and Goris, A and Sondergaard, HB and Sellebjerg, F and Sorensen, PS and Ullum, H and Thorner, LW and Saarela, J and Cournu-Rebeix, I and Damotte, V and Fontaine, B and Guillot-Noel, L and Lathrop, M and Vukusic, S and Berthele, A and Pongratz, V and Gasperi, C and Graetz, C and Grummel, V and Hemmer, B and Hoshi, M and Knier, B and Korn, T and Lill, CM and Luessi, F and Muhlau, M and Zipp, F and Dardiotis, E and Agliardi, C and Amoroso, A and Barizzone, N and Benedetti, MD and Bernardinelli, L and Cavalla, P and Clarelli, F and Comi, G and Cusi, D and Esposito, F and Ferre, L and Galimberti, D and Guaschino, C and Leone, MA and Martinelli, V and Moiola, L and Salvetti, M and Sorosina, M and Vecchio, D and Zauli, A and Santoro, S and Mancini, N and Zuccala, M and Mescheriakova, J and van Duijn, C and Bos, SD and Celius, EG and Spurkland, A and Comabella, M and Montalban, X and Alfredsson, L and Bomfim, IL and Gomez-Cabrero, D and Hillert, J and Jagodic, M and Linden, M and Piehl, F and Jelcic, I and Martin, R and Sospedra, M and Baker, A and Ban, M and Hawkins, C and Hysi, P and Kalra, S and Karpe, F and Khadake, J and Lachance, G and Molyneux, P and Neville, M and Thorpe, J and ... and Australia New Zealand IBDGC and Int Multiple Sclerosis Genetics Co and Initiative Crohn Colitis and Belgium Genetic Consortiumt and United Kingdom IBDGC and ANZgene and WTCCC2 and IIBDGC and NIDDK IBDGCJ and Wellcome Trust Case Control Conso and International Multiple Sclerosis Genetics Consortium and Örebro universitet and Institutionen för medicinska vetenskaper
SCIENCE, ISSN 0036-8075, 09/2019, Volume 365, Issue 6460, pp. 1417 - 1417
Journal Article
by Baranzini, Sergio E and Khankhanian, Pouya and Patsopoulos, Nikolaos A and Li, Michael and Stankovich, Jim and Cotsapas, Chris and Søndergaard, Helle Bach and Ban, Maria and Barizzone, Nadia and Bergamaschi, Laura and Booth, David and Buck, Dorothea and Cavalla, Paola and Celius, Elisabeth G and Comabella, Manuel and Comi, Giancarlo and Compston, Alastair and Cournu-Rebeix, Isabelle and D’alfonso, Sandra and Damotte, Vincent and Din, Lennox and Dubois, Bénédicte and Elovaara, Irina and Esposito, Federica and Fontaine, Bertrand and Franke, Andre and Goris, An and Gourraud, Pierre-Antoine and Graetz, Christiane and Guerini, Franca R and Guillot-Noel, Léna and Hafler, David and Hakonarson, Hakon and Hall, Per and Hamsten, Anders and Harbo, Hanne F and Hemmer, Bernhard and Hillert, Jan and Kemppinen, Anu and Kockum, Ingrid and Koivisto, Keijo and Larsson, Malin and Lathrop, Mark and Leone, Maurizio and Lill, Christina M and Macciardi, Fabio and Martin, Roland and Martinelli, Vittorio and Martinelli-Boneschi, Filippo and McCauley, Jacob L and Myhr, Kjell-Morten and Naldi, Paola and Olsson, Tomas and Oturai, Annette and Pericak-Vance, Margaret A and Perla, Franco and Reunanen, Mauri and Saarela, Janna and Saker-Delye, Safa and Salvetti, Marco and Sellebjerg, Finn and Sørensen, Per Soelberg and Spurkland, Anne and Stewart, Graeme and Taylor, Bruce and Tienari, Pentti and Winkelmann, Juliane and Zipp, Frauke and Ivinson, Adrian J and Haines, Jonathan L and Sawcer, Stephen and DeJager, Philip and Hauser, Stephen L and Oksenberg, Jorge R and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and International Multiple Sclerosis Genetics Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 06/2013, Volume 92, Issue 6, pp. 854 - 865
Journal Article
Nature communications, ISSN 2041-1723, 06/2018, Volume 9, Issue 1, pp. 2397 - 15
Journal Article