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Journal of Medical Genetics, ISSN 0022-2593, 12/2015, Volume 52, Issue 12, pp. 848 - 855
ObjectiveA recent large-scale study in multiple sclerosis (MS) using the ImmunoChip platform reported on 11 loci that showed suggestive genetic association... 
VARIANTS | GENETIC RISK | DISEASE | GUIDELINES | GENETICS & HEREDITY | POWER | DIAGNOSTIC-CRITERIA | LINKAGE | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | Risk Factors | Multiple Sclerosis - genetics | Polymorphism, Single Nucleotide | Genetic Loci | Case-Control Studies | Multiple sclerosis | Usage | Genetic aspects | Risk factors | Meta-analysis
Journal Article
by Antel, Jack and Ban, Maria and Baranzini, Sergio and Barcellos, Lisa and Barizzone, Nadia and Beecham, Ashley and Berge, Tone and Bernardinelli, Luisa and Booth, David and Bos, Steffan and Buck, Dorothea and Butkiewicz, Mariusz and Celius, Elisabeth G and Comabella, Manuel and Compston, Alastair and Dedham, Katrina and Cotsapas, Chris and D’ Alfonso, Sandra and De Jager, Phil and Dubois, Benedicte and Duquette, Pierre and Fontaine, Bertrand and Gasperi, Christiane and Gil, Elia and Goris, An and Gourraud, Pierre Antoine and Graetz, Christiane and Gyllenberg, Alexandra and Hadjigeorgiou, Georgios and Hafler, David and Hribko, Deanna and Haines, Jonathan and Harbo, Hanne and Hauser, Stephen and Warto, Shannon and Hawkins, Clive and Hemmer, Bernhard and Henry, Roland and Hintzen, Rogier and Horakova, Dana and Ivinson, Adrian and Howard, Melissa and Jelcic, Ilijas and Kaskow, Belinda and Kira, Jun-Ichi and Kleinova, Pavlina and Kockum, Ingrid and Kucerova, Karolina and Lill, Christina and Luessi, Felix and Malhotra, Sunny and Martin, Roland and Martinelli, Filippo and Matsushita, Takuya and McCabe, Cristin and McCauley, Jacob and Mescheriakkova, Julia and Mitrovic, Mitja and Moen, Stine-Marit and Montalban, Xavier and Muhlau, Mark and Nakmura, Yuri and Oksenberg, Jorge and Olsson, Tomas and Oturai, Annette and Palotie, Aarno and Patsopoulos, Nikolaos and Pavlicova, Jana and Pericak-Vance, Peggy and Piehl, Fredrik and Rebeix, Isabelle and Rioux, John and Saarela, Janna and Sawcer, Stephen and Sellebjerg, Finn and Sondergaard, Helle Bach and Sorensen, Per Soelberg and Sospedra, Mireia and Spurkland, Anne and Stewart, Graeme and Taylor, Bruce and Uitterlinden, Andre and Van Duijn, Cornelia and Zipp, Frauke and Int Multiple Sclerosis Genetics Co
Neuron, ISSN 0896-6273, 10/2016, Volume 92, Issue 2, pp. 333 - 335
A recent study by claims that the low-frequency variant p.Arg415Gln is sufficient to cause multiple sclerosis in certain individuals and determines a patient’s... 
CYP27B1 GENE | NO EVIDENCE | HUMAN-DISEASE | VARIANTS | NEUROSCIENCES | Multiple sclerosis | Glutamine | Consortia | Genomes | Stratigraphy | Genealogy | Meta-analysis
Journal Article
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
Nature Genetics, ISSN 1061-4036, 09/2015, Volume 47, Issue 10, pp. 1107 - 1113
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
Dermatologic Therapy, ISSN 1396-0296, 05/2019, Volume 32, Issue 3, pp. e12901 - n/a
The management of metastatic melanoma has been transformed by the development of immune checkpoint inhibitors. However, disease control in patients with... 
melanoma | interleukin 2 | checkpoint inhibitors | PD‐L1 | PD-L1 | NIVOLUMAB | NKTR-214 | IMIQUIMOD | DERMATOLOGY | Immune response | Metastasis | Interleukins | Melanoma
Journal Article
Journal Article
NeuroImage, ISSN 1053-8119, 07/2016, Volume 134, pp. 281 - 294
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 4/2019, Volume 25, Issue 5, pp. 661 - 668
Journal Article