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All papers authored by An Goris

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2021 Ide Smets

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, An Goris

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, Marijne Vandebergh

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, Jelle Demeestere

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, Stefan Sunaert

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, Patrick Dupont

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, Bénédicte Dubois

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Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients

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2020 Emanuela Oldoni, Ide Smets, Klara Mallants, Marijne Vandebergh, Lies Van Horebeek, Koen Poesen, Patrick Dupont

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, Bénédicte Dubois, An Goris

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CHIT1 at Diagnosis Reflects Long‐Term Multiple Sclerosis Disease Activity

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2016 Anisha Keshavan, Friedemann Paul, Mona K. Beyer, Alyssa H. Zhu, Nico Papinutto, Russell T. Shinohara, William Stern, Michael Amann, Rohit Bakshi, Antje Bischof, Alessandro Carriero, Manuel Comabella, Jason C. Crane, Sandra D'Alfonso, Sandra D’Alfonso and 49 other authors

Power Estimation for Non-Standardized Multisite Studies

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Seth L. Masters

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, Vasiliki Lagou, Isabelle Jeru, Paul J. Baker

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, Lien Van Eyck, David A. Parry, Dylan Lawless, Dominic De Nardo, Josselyn E. Garcia Perez, Laura F. Dagley, Caroline L. Holley, James Dooley, Fiona Moghaddas, Emanuela Pasciuto

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, Pierre-Yves Jeandel and 17 other authors

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation

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Rick A. A. van der Spek, Anneke J. van der Kooi, Leonard H. van den Berg, Perry Tc C. van Doormaal, Kristel R. van Eijk, Mamede de Carvalho, Marianne de Visser, Paul I. W. de Bakker, Michael A. van Es, W. van Rheenen, Simone de Jong, Wouter Van Rheenen, Annelot M. Dekker, Russell L. Mclaughlin

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, R. A. A. Van Der Spek and 190 other authors

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

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2015 Loukas Moutsianas, Luke Jostins, Ashley H. Beecham, Alexander T. Dilthey

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, Dionysia K. Xifara, Maria Ban, Tejas S. Shah, Nikolaos A. Patsopoulos, Lars Alfredsson, Carl A. Anderson, Katherine E. Attfield, Sergio E. Baranzini

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, Jeffrey Barrett

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, Thomas M. C. Binder, David Booth and 40 other authors

Class II HLA interactions modulate genetic risk for multiple sclerosis

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Kelly Hilven, An Goris

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Genetic burden mirrors epidemiology of multiple sclerosis

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

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Burden of risk variants correlates with phenotype of multiple sclerosis

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An Goris

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, Marte W. Gustavsen, Ine Pauwels, Steffan D. Bos, Elisabeth Gulowsen Celius, Brechtje van Son, Kjell-Morten Myhr, Gustavsen Mw, Kelly Hilven, Sandra D’Alfonso, Maurizio A. Leone

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, Filippo Martinelli Boneschi, Filippo Martinelli Boneschi, Melissa Sorosina, Giuseppe Liberatore and 42 other authors

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

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2014 Laura Ll Kilarski, Sefanja Achterberg, Wj J. Devan, Matthew Traylor, Rainer Malik, Lars Röennblom, Arne Lindgren, Guillame Pare, Pankaj Sharma, Agniesczka Slowik, Vincent Thijs, Matthew Walters, Bradford Bb Worrall, Michele Mm Sale, Ale Algra and 42 other authors

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.

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P. T. van Doormaal, Perry T. C. van Doormaal, Nicola Ticozzi

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, Cinzia Gellera

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, Antonia Ratti, Franco Taroni, Adriano Chio, Andrea Calvo, Gabriele Mora, Gabriella Restagno, Bryan J. Traynor, Anna Birve, Robin Lemmens, Michael A. van Es, Christiaan G. J. Saris and 30 other authors

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

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2013 Sarah Debray, Valérie Race, Veerle Crabbé, Sarah Herdewyn, Gert Matthijs, An Goris

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, Bénédicte Dubois, Vincent Thijs, Wim Robberecht, Philip Van Damme

Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study

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Kim Pannemans, Bieke Broux, An Goris

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, Bénédicte Dubois, Tom Broekmans, Bart Van Wijmeersch, Daniel Geraghty, Piet Stinissen, Niels Hellings

HLA-E restricted CD8+ T cell subsets are phenotypically altered in multiple sclerosis patients

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Imsgc, Alessia di Sapio, Cornelia van Duijn, Wellcome Trust Case Control Consor, Dionysia K. Xifara, Ashley-H. Beecham, Wtccc2, Nikolaos-A. Patsopoulos, Barcellos Lf 2. Wellcome Trust Case Control Consortium, Mary F. Davis, Trust Case Control Consortium 2. Wellcome, Wellcome Trust Case Control Consortium 2 ( Wtccc2), International Multiple Sclerosis Genetics Consortium (Imsgc), Ts-S. Shah, Beecham Ah and 250 other authors

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

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Ine Pauwels, Leentje Cosemans, Steven Boonen, Bénédicte Dubois, An Goris

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Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease

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Sørensen Ps, Hauser Sl, Pouya Khankhanian, Nikolaos A. Patsopoulos, Michael Li, Jim Stankovich, Helle Bach Søndergaard, Gourraud Pa, Chris Cotsapas, Patsopoulos Na, Søndergaard Hb, Isabelle Cournu-Rebeix, Sandra D’alfonso, Sergio E. Baranzini, Vincent Damotte and 79 other authors

Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls

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Dorothea Buck, An Goris

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, Bernhard Hemmer

Reply to Dr Pandey

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2012 Dorothea Buck, Eva Albrecht, Muhammad Aslam, An Goris

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, Natalie Hauenstein, Angela Jochim, Sabine Cepok, Verena Grummel, Bénédicte Dubois, Achim Berthele, Peter Lichtner, Christian Gieger

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, Juliane Winkelmann, Bernhard Hemmer

Genetic Variants in the Immunoglobulin Heavy Chain Locus are Associated with the IgG Index in Multiple Sclerosis

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An Goris

ORCID

, Ine Pauwels, Bénédicte Dubois

Progress in Multiple Sclerosis Genetics

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Robin Lemmens, Alessandra Maugeri, Hans W. M. Niessen, An Goris

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, Thomas Tousseyn

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, Philippe Demaerel, Anniek Corveleyn, Wim Robberecht, Marjo S. van der Knaap, Vincent N. Thijs, Petra J. G. Zwijnenburg

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

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