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Elodie Gautier
Researcher at University of Burgundy
Publications - 40
Citations - 2339
Elodie Gautier is an academic researcher from University of Burgundy. The author has contributed to research in topics: Marfan syndrome & Corticogenesis. The author has an hindex of 19, co-authored 40 publications receiving 1989 citations. Previous affiliations of Elodie Gautier include Claude Bernard University Lyon 1 & French Institute of Health and Medical Research.
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Journal ArticleDOI
Effect of mutation type and location on clinical outcome in 1,013 probands with marfan syndrome or related phenotypes and FBN1 mutations : An international study
Laurence Faivre,Gwenaëlle Collod-Béroud,Gwenaëlle Collod-Béroud,Bart Loeys,Anne H. Child,Christine Binquet,Elodie Gautier,Bert Callewaert,Eloisa Arbustini,Kenneth H. Mayer,Mine Arslan-Kirchner,A Kiotsekoglou,P Comeglio,Nicola Marziliano,Hal Dietz,Dorothy Halliday,Christophe Béroud,Christophe Béroud,Claire Bonithon-Kopp,Mireille Claustres,Christine Muti,H. Plauchu,Peter N. Robinson,Lesley C. Adès,Andrew Biggin,B. Benetts,Maggie Brett,Katherine Holman,J. De Backer,Paul Coucke,Uta Francke,A. De Paepe,Guillaume Jondeau,Catherine Boileau +33 more
TL;DR: In this paper, the authors investigated the correlation between the fibrillin-1 (FBN1) genotype and the nature and severity of the clinical phenotype, including skeletal, cardiovascular, ophthalmologic, skin, pulmonary, and dural.
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Precursor diversity and complexity of lineage relationships in the outer subventricular zone of the primate.
Marion Betizeau,Marion Betizeau,Veronique Cortay,Veronique Cortay,Dorothée Patti,Dorothée Patti,Sabina Pfister,Elodie Gautier,Elodie Gautier,Angele Bellemin-Menard,Angele Bellemin-Menard,Marielle Afanassieff,Marielle Afanassieff,C. Huissoud,C. Huissoud,Rodney J. Douglas,Henry Kennedy,Henry Kennedy,Colette Dehay,Colette Dehay +19 more
TL;DR: It is shown that primate cortical neurons are generated through complex lineages by a mosaic of precursors, thereby providing an innovative framework for understanding specific features of primate corticogenesis.
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Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex
Louis-Jan Pilaz,Dorothée Patti,Guillaume Marcy,Edouard Ollier,Sabina Pfister,Rodney J. Douglas,Marion Betizeau,Elodie Gautier,Veronique Cortay,Nathalie Doerflinger,Henry Kennedy,Colette Dehay +11 more
TL;DR: Modeling confirms that the TG1-induced changes in neuron production and laminar fate are mediated via the changes in the mode of division, and points to the G1 mode ofdivision relationship as an essential control mechanism of corticogenesis.
Journal ArticleDOI
Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.
Laurence Faivre,Alice Masurel-Paulet,Gwenaëlle Collod-Béroud,Bert Callewaert,Anne H. Child,Chantal Stheneur,Christine Binquet,Elodie Gautier,Bertrand Chevallier,Frédéric Huet,Bart Loeys,Eloisa Arbustini,Karin Mayer,Mine Arslan-Kirchner,Anatoli Kiotsekoglou,P Comeglio,Maurizia Grasso,Dorothy Halliday,Christophe Béroud,Claire Bonithon-Kopp,Mireille Claustres,Peter N. Robinson,Lesley C. Adès,Julie De Backer,Paul Coucke,Uta Francke,Anne De Paepe,Catherine Boileau,Guillaume Jondeau +28 more
TL;DR: It is confirmed that the majority of clinical manifestations of Marfan syndrome increase with age, which emphasizes the poor applicability of the international criteria to this diagnosis in childhood and the need for follow-up monitoring in cases of clinical suspicion of Mar fan syndrome.
Journal ArticleDOI
Cardiovascular manifestations in men and women carrying a FBN1 mutation
Delphine Detaint,Laurence Faivre,Gwenaëlle Collod-Béroud,Gwenaëlle Collod-Béroud,Anne H. Child,Bart Loeys,Christine Binquet,Elodie Gautier,Eloisa Arbustini,Karin Mayer,Mine Arslan-Kirchner,Chantal Stheneur,Dorothy Halliday,Christophe Béroud,Christophe Béroud,Claire Bonithon-Kopp,Mireille Claustres,Mireille Claustres,Henri Plauchu,Peter N. Robinson,Anatoli Kiotsekoglou,Julie De Backer,Lesley C. Adès,Lesley C. Adès,Uta Francke,Anne De Paepe,Catherine Boileau,Guillaume Jondeau +27 more
TL;DR: The CV risk remains important in patients with an FBN1 gene mutation and is present throughout life, justifying regular aortic monitoring and thorough examination for extra-aortic features and comprehensive pedigree investigation.