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1.

Human immune diversity: from evolution to modernity.

Liston, Adrian; Humblet-Baron, Stephanie; Duffy, Darragh; Goris, An.

Nat Immunol; 22(12): 1479-1489, 2021 12.

Artículo en Inglés | MEDLINE | ID: mdl-34795445

2.

The cellular composition of the human immune system is shaped by age and cohabitation.

Carr, Edward J; Dooley, James; Garcia-Perez, Josselyn E; Lagou, Vasiliki; Lee, James C; Wouters, Carine; Meyts, Isabelle; Goris, An; Boeckxstaens, Guy; Linterman, Michelle A; Liston, Adrian.

Nat Immunol; 17(4): 461-468, 2016 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-26878114

3.

Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation.

Carr, Edward J; Dooley, James; Garcia-Perez, Josselyn E; Lagou, Vasiliki; Lee, James C; Wouters, Carine; Meyts, Isabelle; Goris, An; Boeckxstaens, Guy; Linterman, Michelle A; Liston, Adrian.

Nat Immunol; 22(2): 254, 2021 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-33239822

4.

The origins of diversity in human immunity.

Liston, Adrian; Goris, An.

Nat Immunol; 19(3): 209-210, 2018 03.

Artículo en Inglés | MEDLINE | ID: mdl-29476185

5.

Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.

Vandebergh, Marijne; Andlauer, Till F M; Zhou, Yuan; Mallants, Klara; Held, Friederike; Aly, Lilian; Taylor, Bruce V; Hemmer, Bernhard; Dubois, Bénédicte; Goris, An.

Ann Neurol; 89(5): 884-894, 2021 05.

Artículo en Inglés | MEDLINE | ID: mdl-33704824

6.

A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease.

Van Horebeek, Lies; Hilven, Kelly; Mallants, Klara; Van Nieuwenhuijze, Annemarie; Kelkka, Tiina; Savola, Paula; Mustjoki, Satu; Schlenner, Susan M; Liston, Adrian; Dubois, Bénédicte; Goris, An.

Hum Mol Genet; 28(8): 1369-1380, 2019 04 15.

Artículo en Inglés | MEDLINE | ID: mdl-30541027

7.

CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity.

Oldoni, Emanuela; Smets, Ide; Mallants, Klara; Vandebergh, Marijne; Van Horebeek, Lies; Poesen, Koen; Dupont, Patrick; Dubois, Bénédicte; Goris, An.

Ann Neurol; 87(4): 633-645, 2020 04.

Artículo en Inglés | MEDLINE | ID: mdl-31997416

8.

IFN-Î³ stimulates CpG-induced IL-10 production in B cells via p38 and JNK signalling pathways.

Imbrechts, Maya; De Samblancx, Karen; Fierens, Karlien; Brisse, Ellen; Vandenhaute, Jessica; Mitera, Tania; Libert, Claude; Smets, Ide; Goris, An; Wouters, Carine; Matthys, Patrick.

Eur J Immunol; 48(9): 1506-1521, 2018 09.

Artículo en Inglés | MEDLINE | ID: mdl-30004580

9.

Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes.

Van Nieuwenhove, Erika; Lagou, Vasiliki; Van Eyck, Lien; Dooley, James; Bodenhofer, Ulrich; Roca, Carlos; Vandebergh, Marijne; Goris, An; Humblet-Baron, Stéphanie; Wouters, Carine; Liston, Adrian.

Ann Rheum Dis; 78(5): 617-628, 2019 05.

Artículo en Inglés | MEDLINE | ID: mdl-30862608

10.

Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.

Smets, Ide; Fiddes, Barnaby; Garcia-Perez, Josselyn E; He, Di; Mallants, Klara; Liao, Wenjia; Dooley, James; Wang, George; Humblet-Baron, Stephanie; Dubois, Bénédicte; Compston, Alastair; Jones, Joanne; Coles, Alasdair; Liston, Adrian; Ban, Maria; Goris, An; Sawcer, Stephen.

Brain; 141(3): 786-796, 2018 03 01.

Artículo en Inglés | MEDLINE | ID: mdl-29361022

11.

Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.

Staats, Kim A; Humblet-Baron, Stephanie; Bento-Abreu, Andre; Scheveneels, Wendy; Nikolaou, Alexandros; Deckers, Kato; Lemmens, Robin; Goris, An; Van Ginderachter, Jo A; Van Damme, Philip; Hisatsune, Chihiro; Mikoshiba, Katsuhiko; Liston, Adrian; Robberecht, Wim; Van Den Bosch, Ludo.

Hum Mol Genet; 25(16): 3491-3499, 2016 08 15.

Artículo en Inglés | MEDLINE | ID: mdl-27378687

12.

Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.

Hilven, Kelly; Vandebergh, Marijne; Smets, Ide; Mallants, Klara; Goris, An; Dubois, Bénédicte.

Mult Scler; 24(13): 1773-1775, 2018 11.

Artículo en Inglés | MEDLINE | ID: mdl-29303040

13.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

Sawcer, Stephen; Hellenthal, Garrett; Pirinen, Matti; Spencer, Chris C A; 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.

Nature; 476(7359): 214-9, 2011 Aug 10.

Artículo en Inglés | MEDLINE | ID: mdl-21833088

14.

Power estimation for non-standardized multisite studies.

Keshavan, Anisha; Paul, Friedemann; Beyer, Mona K; Zhu, Alyssa H; Papinutto, Nico; Shinohara, Russell T; Stern, William; Amann, Michael; Bakshi, Rohit; Bischof, Antje; Carriero, Alessandro; Comabella, Manuel; Crane, Jason C; D'Alfonso, Sandra; Demaerel, Philippe; Dubois, Benedicte; Filippi, Massimo; Fleischer, Vinzenz; Fontaine, Bertrand; Gaetano, Laura; Goris, An; Graetz, Christiane; Gröger, Adriane; Groppa, Sergiu; Hafler, David A; Harbo, Hanne F; Hemmer, Bernhard; Jordan, Kesshi; Kappos, Ludwig; Kirkish, Gina; Llufriu, Sara; Magon, Stefano; Martinelli-Boneschi, Filippo; McCauley, Jacob L; Montalban, Xavier; Mühlau, Mark; Pelletier, Daniel; Pattany, Pradip M; Pericak-Vance, Margaret; Cournu-Rebeix, Isabelle; Rocca, Maria A; Rovira, Alex; Schlaeger, Regina; Saiz, Albert; Sprenger, Till; Stecco, Alessandro; Uitdehaag, Bernard M J; Villoslada, Pablo; Wattjes, Mike P; Weiner, Howard.

Neuroimage; 134: 281-294, 2016 07 01.

Artículo en Inglés | MEDLINE | ID: mdl-27039700

15.

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.

Goris, An; van Setten, Jessica; Diekstra, Frank; Ripke, Stephan; Patsopoulos, Nikolaos A; Sawcer, Stephen J; van Es, Michael; Andersen, Peter M; Melki, Judith; Meininger, Vincent; Hardiman, Orla; Landers, John E; Brown, Robert H; Shatunov, Aleksey; Leigh, Nigel; Al-Chalabi, Ammar; Shaw, Christopher E; Traynor, Bryan J; Chiò, Adriano; Restagno, Gabriella; Mora, Gabriele; Ophoff, Roel A; Oksenberg, Jorge R; Van Damme, Philip; Compston, Alastair; Robberecht, Wim; Dubois, Bénédicte; van den Berg, Leonard H; De Jager, Philip L; Veldink, Jan H; de Bakker, Paul I W.

Hum Mol Genet; 23(7): 1916-22, 2014 Apr 01.

Artículo en Inglés | MEDLINE | ID: mdl-24234648

16.

Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.

Goris, An; Pauwels, Ine; Gustavsen, Marte W; van Son, Brechtje; Hilven, Kelly; Bos, Steffan D; Celius, Elisabeth Gulowsen; Berg-Hansen, Pål; Aarseth, Jan; Myhr, Kjell-Morten; D'Alfonso, Sandra; Barizzone, Nadia; Leone, Maurizio A; Martinelli Boneschi, Filippo; Sorosina, Melissa; Liberatore, Giuseppe; Kockum, Ingrid; Olsson, Tomas; Hillert, Jan; Alfredsson, Lars; Bedri, Sahl Khalid; Hemmer, Bernhard; Buck, Dorothea; Berthele, Achim; Knier, Benjamin; Biberacher, Viola; van Pesch, Vincent; Sindic, Christian; Bang Oturai, Annette; Søndergaard, Helle Bach; Sellebjerg, Finn; Jensen, Poul Erik H; Comabella, Manuel; Montalban, Xavier; Pérez-Boza, Jennifer; Malhotra, Sunny; Lechner-Scott, Jeannette; Broadley, Simon; Slee, Mark; Taylor, Bruce; Kermode, Allan G; Gourraud, Pierre-Antoine; Sawcer, Stephen J; Andreassen, Bettina Kullle; Dubois, Bénédicte; Harbo, Hanne F.

Brain; 138(Pt 3): 632-43, 2015 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-25616667

17.

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.

Gregory, Simon G; Schmidt, Silke; Seth, Puneet; Oksenberg, Jorge R; Hart, John; Prokop, Angela; Caillier, Stacy J; Ban, Maria; Goris, An; Barcellos, Lisa F; Lincoln, Robin; McCauley, Jacob L; Sawcer, Stephen J; Compston, D A S; Dubois, Benedicte; Hauser, Stephen L; Garcia-Blanco, Mariano A; Pericak-Vance, Margaret A; Haines, Jonathan L.

Nat Genet; 39(9): 1083-91, 2007 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-17660817

18.

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency.

Lemmens, Robin; Maugeri, Alessandra; Niessen, Hans W M; Goris, An; Tousseyn, Thomas; Demaerel, Philippe; Corveleyn, Anniek; Robberecht, Wim; van der Knaap, Marjo S; Thijs, Vincent N; Zwijnenburg, Petra J G.

Hum Mol Genet; 22(2): 391-7, 2013 Jan 15.

Artículo en Inglés | MEDLINE | ID: mdl-23065703

19.

Burden of risk variants correlates with phenotype of multiple sclerosis.

Hilven, Kelly; Patsopoulos, Nikolaos A; Dubois, Bénédicte; Goris, An.

Mult Scler; 21(13): 1670-80, 2015 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-25948629

20.

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis.

Herdewyn, Sarah; Zhao, Hui; Moisse, Matthieu; Race, Valérie; Matthijs, Gert; Reumers, Joke; Kusters, Benno; Schelhaas, Helenius J; van den Berg, Leonard H; Goris, An; Robberecht, Wim; Lambrechts, Diether; Van Damme, Philip.

Hum Mol Genet; 21(11): 2412-9, 2012 Jun 01.

Artículo en Inglés | MEDLINE | ID: mdl-22343411

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