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Emilie Théâtre
Researcher at University of Liège
Publications - 9
Citations - 1044
Emilie Théâtre is an academic researcher from University of Liège. The author has contributed to research in topics: Crohn's disease & Signal transduction. The author has an hindex of 9, co-authored 9 publications receiving 851 citations.
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Journal ArticleDOI
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
Isabelle Cleynen,Isabelle Cleynen,Gabrielle Boucher,Luke Jostins,Luke Jostins,Luke Jostins,L. Philip Schumm,Sebastian Zeissig,Tariq Ahmad,Vibeke Andersen,Jane M. Andrews,Jane M. Andrews,Vito Annese,Stephan Brand,Steven R. Brant,Judy H. Cho,Mark J. Daly,Marla Dubinsky,Richard H. Duerr,Lynnette R. Ferguson,Andre Franke,Richard B. Gearry,Richard B. Gearry,Philippe Goyette,Hakon Hakonarson,Jonas Halfvarson,Johannes R. Hov,Hailang Huang,Nicholas A. Kennedy,Limas Kupčinskas,Ian C. Lawrance,James Lee,Jack Satsangi,Stephan Schreiber,Emilie Théâtre,Andrea E. van der Meulen-de Jong,Rinse K. Weersma,David C. Wilson,David C. Wilson,Miles Parkes,Severine Vermeire,John D. Rioux,John C. Mansfield,Mark S. Silverberg,Graham L. Radford-Smith,Graham L. Radford-Smith,Dermot P.B. McGovern,Jeffrey C. Barrett,Charlie W. Lees +48 more
TL;DR: The largest genotype association study, to date, in widely used clinical subphenotypes of inflammatory bowel disease with the goal of further understanding the biological relations between diseases.
Journal ArticleDOI
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Dalia Kasperavičiūtė,Claudia B. Catarino,Claudia B. Catarino,Mar Matarin,Costin Leu,Jan Novy,Jan Novy,Anna Tostevin,Anna Tostevin,Bárbara Leal,Ellen V. S. Hessel,Kerstin Hallmann,Michael S. Hildebrand,Hans-Henrik M. Dahl,Mina Ryten,Daniah Trabzuni,Adaikalavan Ramasamy,Adaikalavan Ramasamy,Saud Alhusaini,Saud Alhusaini,Colin P. Doherty,Thomas Dorn,Jörg Hansen,Günter Krämer,Bernhard J. Steinhoff,Dominik Zumsteg,Susan Duncan,Reetta Kälviäinen,Kai Eriksson,Anne-Mari Kantanen,Massimo Pandolfo,Ursula Gruber-Sedlmayr,Kurt Schlachter,Eva M. Reinthaler,Elisabeth Stögmann,Fritz Zimprich,Emilie Théâtre,Colin Smith,Terence J. O'Brien,Terence J. O'Brien,K. Meng Tan,K. Meng Tan,Slavé Petrovski,Slavé Petrovski,Angela Robbiano,Roberta Paravidino,Federico Zara,Pasquale Striano,Michael R. Sperling,Russell J. Buono,Hakon Hakonarson,João Chaves,Paulo Costa,Paulo Costa,Berta Martins da Silva,António Martins da Silva,Pierre N. E. De Graan,Bobby P. C. Koeleman,Albert J. Becker,Susanne Schoch,Marec von Lehe,Philipp S. Reif,Felix Rosenow,Felicitas Becker,Yvonne G. Weber,Holger Lerche,Karl Rössler,Michael Buchfelder,Hajo M. Hamer,Katja Kobow,Roland Coras,Ingmar Blümcke,Ingrid E. Scheffer,Ingrid E. Scheffer,Ingrid E. Scheffer,Samuel F. Berkovic,Michael E. Weale,Norman Delanty,Norman Delanty,Chantal Depondt,Gianpiero L. Cavalleri,Wolfram S. Kunz,Sanjay M. Sisodiya,Sanjay M. Sisodiya +83 more
TL;DR: Genetic analysis and meta-analysis suggest SCN1A involvement in a common epilepsy syndrome, give new direction to biological understanding of mesial temporal lobe epilepsy with hippocampal sclerosis with febrile seizures, and open avenues for investigation of prognostic factors and possible prevention of epilepsy in some children with febs.
Journal ArticleDOI
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes
Yukihide Momozawa,Julia Dmitrieva,Emilie Théâtre,Valérie Deffontaine,Souad Rahmouni,Benoit Charloteaux,François Crins,Elisa Docampo,Mahmoud Elansary,Ann Stephan Gori,Christelle Lecut,Rob Mariman,Myriam Mni,Cécile Oury,Ilya Altukhov,Dmitry G. Alexeev,Yuri Aulchenko,Leila Amininejad,Gerd Bouma,Frank Hoentjen,Mark Löwenberg,Bas Oldenburg,Marieke Pierik,Andrea E. Vander Meulen-De Jong,C. Janneke van der Woude,Marijn C. Visschedijk,Mark Lathrop,Jean-Pierre Hugot,Rinse K. Weersma,Martine De Vos,Denis Franchimont,Severine Vermeire,Michiaki Kubo,Edouard Louis,Michel Georges +34 more
TL;DR: The authors provide eQTL datasets for six circulating immune cell types and ileal, colonic and rectal biopsies to map regulatory modules and identify potential causative genes for IBD.
Journal ArticleDOI
Dual-Specificity Phosphatase 3 Deficiency or Inhibition Limits Platelet Activation and Arterial Thrombosis
Lucia Musumeci,Marijke J.E. Kuijpers,Karen Gilio,Alexandre Hego,Emilie Théâtre,Lisbeth Maurissen,Maud Vandereyken,Catia V Diogo,Christelle Lecut,William Guilmain,Ekaterina V. Bobkova,Johannes A. Eble,Russell Dahl,Pierre Drion,Justin Rascon,Yalda Mostofi,Hongbin Yuan,Eduard Sergienko,Thomas D.Y. Chung,Marc Thiry,Yotis A. Senis,Michel Moutschen,Tomas Mustelin,Patrizio Lancellotti,Johan W. M. Heemskerk,Lutz Tautz,Cécile Oury,Souad Rahmouni +27 more
TL;DR: In this paper, the dual-specificity phosphatase 3 (DUSP3) was found to be a critical regulator of platelet activation and thrombosis.
Journal ArticleDOI
The TNF/ADAM 17 system: implication of an ADAM 17 haplotype in the clinical response to infliximab in Crohn's disease
Vinciane Dideberg,Emilie Théâtre,Frédéric Farnir,Severine Vermeire,Paul Rutgeerts,Martine De Vos,Jacques Belaiche,Denis Franchimont,André Van Gossum,Edouard Louis,Vincent Bours +10 more
TL;DR: The results exclude, with a reasonable power, an implication of the TNF gene in the response to infliximab in Crohn's disease, but reveal a potential role of the ADAM 17 gene in this response.