Caroline Demily - Publications

Affiliations: 
Universite Lyon 1, Villeurbanne, Auvergne-Rhône-Alpes, France 

66 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Gauld C, Poisson A, Reversat J, Peyroux E, Houdayer-Robert F, Rossi M, Lesca G, Sanlaville D, Demily C. Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review. Bmc Psychiatry. 21: 360. PMID 34273950 DOI: 10.1186/s12888-021-03342-8  1
2021 Dubreucq M, Plasse J, Gabayet F, Blanc O, Chereau I, Cervello S, Couhet G, Demily C, Guillard-Bouhet N, Gouache B, Jaafari N, Legrand G, Legros-Lafarge E, Mora G, Pommier R, et al. Sex Differences in Recovery-Related Outcomes and Needs for Psychiatric Rehabilitation in People With Schizophrenia Spectrum Disorder. The Journal of Clinical Psychiatry. 82. PMID 34010524 DOI: 10.4088/JCP.20m13732  1
2021 Poncet F, Soussignan R, Jaffiol M, Gaudelus B, Leleu A, Demily C, Franck N, Baudouin JY. The spatial distribution of eye movements predicts the (false) recognition of emotional facial expressions. Plos One. 16: e0245777. PMID 33497409 DOI: 10.1371/journal.pone.0245777  1
2020 Gomez A, Costa M, Lio G, Sirigu A, Demily C. Face first impression of trustworthiness in Williams Syndrome: Dissociating automatic vs decision based perception. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 132: 99-112. PMID 32971481 DOI: 10.1016/J.Cortex.2020.07.015  0.24
2020 Bodemer C, Diociaiuti A, Hadj-Rabia S, Robert MP, Desguerre I, Manière MC, de la Dure-Molla M, De Liso P, Federici M, Galeotti A, Fusco F, Fraitag S, Demily C, Taieb C, Valeria Ursini M, et al. Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti. Journal of the European Academy of Dermatology and Venereology : Jeadv. 34: 1415-1424. PMID 32678511 DOI: 10.1111/jdv.16403  0.01
2020 Poisson A, Chatron N, Labalme A, Fourneret P, Ville D, Mathieu ML, Sanlaville D, Demily C, Lesca G. Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report. Bmc Medical Genetics. 21: 10. PMID 31914951 DOI: 10.1186/S12881-019-0946-0  1
2020 Gauld C, Reversat J, Sanlaville D, Demily C. Les enjeux de la génétique en psychiatrie Evolution Psychiatrique. DOI: 10.1016/J.Evopsy.2020.06.002  1
2019 Munnich A, Demily C, Frugère L, Duwime C, Malan V, Barcia G, Vidal C, Throo É, Besmond C, Hubert L, Roland-Manuel G, Malen JP, Ferreri M, Hanein S, Boddaert N, et al. [Twenty years of on-site clinical genetics consultations for people with ASD]. Medecine Sciences : M/S. 35: 843-851. PMID 31845875 DOI: 10.1051/medsci/2019170  0.01
2019 Faoucher M, Demily C. The psychopharmacology of Wilson disease and other metabolic disorders. Handbook of Clinical Neurology. 165: 191-205. PMID 31727212 DOI: 10.1016/B978-0-444-64012-3.00011-3  0.01
2019 Favre E, Leleu A, Peyroux E, Baudouin JY, Franck N, Demily C. Exploratory case study of monozygotic twins with 22q11.2DS provides further clues to circumscribe neurocognitive markers of psychotic symptoms. Neuroimage. Clinical. 24: 101987. PMID 31446315 DOI: 10.1016/J.Nicl.2019.101987  1
2019 Munnich A, Demily C, Frugère L, Duwime C, Malan V, Barcia G, Vidal C, Throo E, Besmond C, Hubert L, Roland-Manuel G, Malen JP, Ferreri M, Hanein S, Thalabard JC, et al. Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder. Molecular Autism. 10: 33. PMID 31406558 DOI: 10.1186/S13229-019-0284-2  0.01
2019 Poisson A, Nicolas A, Bousquet I, Raverot V, Gronfier C, Demily C. Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder. International Journal of Molecular Sciences. 20. PMID 31330985 DOI: 10.3390/Ijms20143533  1
2019 Masson J, Demily C, Chatron N, Labalme A, Rollat-Farnier PA, Schluth-Bolard C, Gilbert-Dussardier B, Giuliano F, Touraine R, Tordjman S, Verloes A, Testa G, Sanlaville D, Edery P, Lesca G, et al. Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder. Orphanet Journal of Rare Diseases. 14: 121. PMID 31151468 DOI: 10.1186/S13023-019-1094-5  1
2019 Peyroux E, Babinet MN, Cannarsa C, Madelaine C, Favre E, Demily C, Michael GA. What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS? European Child & Adolescent Psychiatry. PMID 31123832 DOI: 10.1007/S00787-019-01345-1  0.01
2019 Demily C, Duwime C, Lopez C, Heminou C, Poisson A, Plasse J, Robert M, Dénier C, Rossi M, Franck N, Besmond C, Barcia G, Boddaert N, Munnich A, Vaivre-Douret L. Corpus callosum metrics predict severity of visuospatial and neuromotor dysfuntions in ARID1B mutations with Coffin-Siris syndrome. Psychiatric Genetics. PMID 30933046 DOI: 10.1097/Ypg.0000000000000225  1
2019 Leleu A, Favre E, Yailian A, Fumat H, Klamm J, Amado I, Baudouin JY, Franck N, Demily C. An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome. Translational Psychiatry. 9: 67. PMID 30718458 DOI: 10.1038/S41398-019-0411-Z  1
2019 Franck N, Bon L, Dekerle M, Plasse J, Massoubre C, Pommier R, Legros-Lafarge E, Jaafari N, Guillard-Bouhet N, Quilès C, Couhet G, Verdoux H, Gouache B, Martin B, Cervello S, ... Demily C, et al. Satisfaction and Needs in Serious Mental Illness and Autism Spectrum Disorder: The REHABase Psychosocial Rehabilitation Project. Psychiatric Services (Washington, D.C.). appips201800420. PMID 30691384 DOI: 10.1176/Appi.Ps.201800420  1
2018 Poisson A, Lesca G, Chatron N, Demily C, Favre E, Cottin V, Gamondes D, Sanlaville D, Edery P, Giraud S, Dupuis-Girod S. 12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome. European Journal of Medical Genetics. PMID 30389587 DOI: 10.1016/j.ejmg.2018.10.017  1
2018 Poisson A, Chatron N, Labalme A, Till M, Broussolle E, Sanlaville D, Demily C, Lesca G. Regressive Autism Spectrum Disorder Expands the Phenotype of BSCL2/Seipin-Associated Neurodegeneration. Biological Psychiatry. PMID 30150100 DOI: 10.1016/J.Biopsych.2018.05.010  1
2018 Favre E, Peyroux E, Babinet MN, Poisson A, Demily C. Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial. Bmc Psychiatry. 18: 235. PMID 30029627 DOI: 10.1186/S12888-018-1810-Z  1
2018 Morel A, Peyroux E, Leleu A, Favre E, Franck N, Demily C. Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype. Frontiers in Pediatrics. 6: 102. PMID 29774207 DOI: 10.3389/Fped.2018.00102  1
2018 Demily C, Lesca G, Poisson A, Till M, Barcia G, Chatron N, Sanlaville D, Munnich A. Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide He Forest? Journal of Autism and Developmental Disorders. PMID 29589274 DOI: 10.1007/S10803-018-3552-7  1
2018 Peyroux E, Rigard C, Saucourt G, Poisson A, Plasse J, Franck N, Demily C. Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia. Early Intervention in Psychiatry. PMID 29575660 DOI: 10.1111/Eip.12557  1
2017 Demily C, Hubert L, Franck N, Poisson A, Munnich A, Besmond C. Somatic mosaicism for SLC1A1 mutation supports threshold effect and familial aggregation in schizophrenia spectrum disorders. Schizophrenia Research. PMID 29195747 DOI: 10.1016/J.Schres.2017.11.028  1
2017 Demily C, Poisson A, Thibaut F, Franck N. Weight loss induced by quetiapine in a 22q11.2DS patient. Molecular Genetics and Metabolism Reports. 13: 95-96. PMID 29062712 DOI: 10.1016/J.Ymgmr.2017.10.002  1
2017 Poisson A, Favre E, Peyroux E, Nicolas A, Schlutz Bolard C, Demily C. An ambiguous psychiatric diagnosis resolved by genetic investigations. Schizophrenia Research. PMID 28943095 DOI: 10.1016/J.Schres.2017.09.022  1
2017 Morel A, Demily C. [Social cognition in children with neurogenetic syndromes: A literature review]. Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie. PMID 28668215 DOI: 10.1016/J.Arcped.2017.05.006  0.01
2017 Mathieu ML, Demily C, Chantot-Bastaraud S, Afenjar A, Mignot C, Andrieux J, Gerard M, Catala-Mora J, Jouk PS, Labalme A, Edery P, Sanlaville D, Rossi M. Clinical and molecular cytogenetic characterization of four unrelated patients carrying 2p14 microdeletions. American Journal of Medical Genetics. Part A. PMID 28599093 DOI: 10.1002/Ajmg.A.38307  1
2017 Demily C, Parant F, Cheillan D, Broussolle E, Pavec A, Guillaud O, Restier L, Lachaux A, Bost M. Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary study. Annals of General Psychiatry. 16: 19. PMID 28392828 DOI: 10.1186/s12991-017-0142-6  0.01
2017 Peyroux E, Santaella N, Broussolle E, Rigard C, Favre E, Brunet AS, Bost M, Lachaux A, Demily C. Social cognition in Wilson's disease: A new phenotype? Plos One. 12: e0173467. PMID 28384152 DOI: 10.1371/Journal.Pone.0173467  1
2017 Poisson A, Roze E, Demily C, Thobois S. Evidence for dopaminergic denervation in classical galactosemia. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28370299 DOI: 10.1002/Mds.26980  1
2017 Demily C, Duwime C, Poisson A, Boddaert N, Munnich A. Authors' reply - Clozapine for mitochondrial psychosis. Molecular Genetics and Metabolism Reports. 10: 101. PMID 28224085 DOI: 10.1016/J.Ymgmr.2017.01.012  1
2017 Demily C, Poisson A, Peyroux E, Gatellier V, Nicolas A, Rigard C, Schluth-Bolard C, Sanlaville D, Rossi M. Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature. Bmc Medical Genetics. 18: 9. PMID 28137251 DOI: 10.1186/S12881-017-0371-1  1
2017 Demily C, Duwime C, Poisson A, Boddaert N, Munnich A. Low dose clozapine controls adult-onset psychosis associated with the neurogenic ataxia-retinitis pigmentosa (NARP) mutation. Molecular Genetics and Metabolism Reports. 10: 20-22. PMID 28003964 DOI: 10.1016/J.Ymgmr.2016.12.003  1
2016 Demily C, Louchart-de-la-Chapelle S, Nkam I, Ramoz N, Denise P, Nicolas A, Savalle C, Thibaut F. Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia? Psychiatry Research. PMID 27825784 DOI: 10.1016/J.Psychres.2016.07.066  1
2016 Boschi A, Planche P, Hemimou C, Demily C, Vaivre-Douret L. From High Intellectual Potential to Asperger Syndrome: Evidence for Differences and a Fundamental Overlap-A Systematic Review. Frontiers in Psychology. 7: 1605. PMID 27812341 DOI: 10.3389/Fpsyg.2016.01605  0.01
2016 Babinet MN, Rigard C, Peyroux É, Dragomir AR, Plotton I, Lejeune H, Demily C. [Social cognition disorders in Klinefelter syndrome: A specific phenotype? (KS)]. L'Encephale. PMID 27743676 DOI: 10.1016/J.Encep.2016.04.010  1
2016 Demily C, Franck N. Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia? European Journal of Medical Genetics. PMID 27639442 DOI: 10.1016/J.Ejmg.2016.09.007  1
2016 Poisson A, Schluth Bolard C, Martin B, Babinet MN, Sanlaville D, Demily C. 16q12.2q21: A new susceptibility locus for schizophrenia? Schizophrenia Research. PMID 27617415 DOI: 10.1016/J.Schres.2016.09.007  1
2016 Demily C, Rigard C, Peyroux E, Chesnoy-Servanin G, Morel A, Franck N. «Cognitus & Moi»: A Computer-Based Cognitive Remediation Program for Children with Intellectual Disability. Frontiers in Psychiatry. 7: 10. PMID 26869942 DOI: 10.3389/Fpsyt.2016.00010  1
2015 Leleu A, Demily C, Franck N, Durand K, Schaal B, Baudouin JY. The Odor Context Facilitates the Perception of Low-Intensity Facial Expressions of Emotion. Plos One. 10: e0138656. PMID 26390036 DOI: 10.1371/Journal.Pone.0138656  1
2015 Poisson A, Nicolas A, Cochat P, Sanlaville D, Rigard C, de Leersnyder H, Franco P, Des Portes V, Edery P, Demily C. Behavioral disturbance and treatment strategies in Smith-Magenis syndrome. Orphanet Journal of Rare Diseases. 10: 111. PMID 26336863 DOI: 10.1186/S13023-015-0330-X  1
2015 Leleu A, Saucourt G, Rigard C, Chesnoy G, Baudouin JY, Rossi M, Edery P, Franck N, Demily C. Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome. European Child & Adolescent Psychiatry. PMID 26149605 DOI: 10.1007/S00787-015-0741-1  1
2015 Poisson A, Nicolas A, Sanlaville D, Cochat P, De Leersnyder H, Rigard C, Franco P, des Portes V, Edery P, Demily C. [Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]. Archives De PéDiatrie : Organe Officiel De La SociéTe FrançAise De PéDiatrie. 22: 638-45. PMID 25934608 DOI: 10.1016/J.Arcped.2015.03.015  1
2015 Franck N, Demily C. [Improving functional outcome of schizophrenia with cognitive remediation]. Presse MéDicale (Paris, France : 1983). 44: 292-7. PMID 25544348 DOI: 10.1016/J.Lpm.2014.06.031  1
2015 Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome]. L'EncéPhale. 41: 266-73. PMID 25523123 DOI: 10.1016/J.Encep.2014.10.005  1
2015 Pillet B, Morvan Y, Todd A, Franck N, Duboc C, Grosz A, Launay C, Demily C, Gaillard R, Krebs MO, Amado I. Cognitive remediation therapy (CRT) benefits more to patients with schizophrenia with low initial memory performances. Disability and Rehabilitation. 37: 846-53. PMID 25109501 DOI: 10.3109/09638288.2014.946153  1
2015 Poisson A, Nicolas A, Cochat P, Sanlaville D, Rigard C, De Leersnyder H, Franco P, Portes VD, Edery P, Demily C. Behavioral disturbance and treatment strategies in Smith-Magenis syndrome Orphanet Journal of Rare Diseases. 10. DOI: 10.1186/s13023-015-0330-x  1
2015 Poisson A, Nicolas A, Sanlaville D, Cochat P, De Leersnyder H, Rigard C, Franco P, des Portes V, Edery P, Demily C. Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders | Le syndrome de Smith-Magenis, une association unique de troubles du comportement et du cycle veille/sommeil Archives De Pediatrie. 22: 638-645. DOI: 10.1016/j.arcped.2015.03.015  1
2014 Demily C, Rossi M, Chesnoy-Servanin G, Martin B, Poisson A, Sanlaville D, Edery P. Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p. Bmc Medical Genetics. 15: 132. PMID 25496186 DOI: 10.1186/S12881-014-0132-3  1
2014 Demily C, Sedel F. Psychiatric manifestations of treatable hereditary metabolic disorders in adults. Annals of General Psychiatry. 13: 27. PMID 25478001 DOI: 10.1186/s12991-014-0027-x  0.01
2013 Franck N, Duboc C, Sundby C, Amado I, Wykes T, Demily C, Launay C, Le Roy V, Bloch P, Willard D, Todd A, Petitjean F, Foullu S, Briant P, Grillon ML, et al. Specific vs general cognitive remediation for executive functioning in schizophrenia: a multicenter randomized trial. Schizophrenia Research. 147: 68-74. PMID 23583327 DOI: 10.1016/J.Schres.2013.03.009  1
2013 Cavard H, Martin B, Lesca G, Saucourt G, Rafat A, Duboc C, d’Amato T, Sanlaville D, Edery P, Demily C. Aneuploïdie 47,XYY et schizophrénie avec troubles du comportement : report de cas et discussion de la littérature European Psychiatry. 28: 27-27. DOI: 10.1016/J.Eurpsy.2013.09.066  1
2012 Bruno N, Sachs N, Demily C, Franck N, Pacherie E. Delusions and metacognition in patients with schizophrenia. Cognitive Neuropsychiatry. 17: 1-18. PMID 22216943 DOI: 10.1080/13546805.2011.562071  1
2011 Demily C, Weiss T, Desmurget M, Franck N, Baudouin JY. Recognition of self-generated facial emotions is impaired in schizophrenia. The Journal of Neuropsychiatry and Clinical Neurosciences. 23: 189-93. PMID 21677248 DOI: 10.1176/Jnp.23.2.Jnp189  1
2009 Demily C, Cavézian C, Desmurget M, Berquand-Merle M, Chambon V, Franck N. The game of chess enhances cognitive abilities in schizophrenia. Schizophrenia Research. 107: 112-3. PMID 18995990 DOI: 10.1016/J.Schres.2008.09.024  1
2009 Legallic S, Bou J, Haouzir S, Allio G, Demily C, Petit M, Frebourg T, Thibaut F, Campion D. No pathogenic rearrangement within the DISC 1 gene in psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 148-50. PMID 18395819 DOI: 10.1002/Ajmg.B.30753  1
2009 Weiss T, Baudouin JY, Demily C. Production of facial expression in schizophrenia Evolution Psychiatrique. 74: 137-144. DOI: 10.1016/J.Evopsy.2008.12.010  1
2008 Demily C, Franck N. Cognitive remediation: a promising tool for the treatment of schizophrenia. Expert Review of Neurotherapeutics. 8: 1029-36. PMID 18590474 DOI: 10.1586/14737175.8.7.1029  1
2008 Demily C, Franck N. Gabapentin for ultra resistant schizophrenia with aggressive behavior. Schizophrenia Research. 100: 349-50. PMID 18255272 DOI: 10.1016/J.Schres.2007.12.482  1
2007 Demily C, Legallic S, Bou J, Houy-Durand E, Van Amelsvoort T, Zinkstok J, Manouvrier-Hanue S, Vogels A, Drouin-Garraud V, Philip N, Philippe A, Héron D, Sarda P, Petit M, Thibaut F, et al. ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia. Psychiatric Genetics. 17: 311-2. PMID 17728672 DOI: 10.1097/Ypg.0B013E328133F369  1
2007 Guillin O, Demily C, Thibaut F. Brain-derived neurotrophic factor in schizophrenia and its relation with dopamine. International Review of Neurobiology. 78: 377-95. PMID 17349867 DOI: 10.1016/S0074-7742(06)78012-6  1
2007 Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, ... ... Demily C, et al. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human Molecular Genetics. 16: 83-91. PMID 17135275 DOI: 10.1093/Hmg/Ddl443  1
2005 Peuskens J, Demily C, Thibaut F. Treatment of cognitive dysfunction in schizophrenia. Clinical Therapeutics. 27: S25-37. PMID 16198199 DOI: 10.1016/j.clinthera.2005.07.015  1
2005 Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, et al. Hyperprolinemia is a risk factor for schizoaffective disorder. Molecular Psychiatry. 10: 479-85. PMID 15494707 DOI: 10.1038/Sj.Mp.4001597  1
2004 Houy E, Raux G, Thibaut F, Belmont A, Demily C, Allio G, Haouzir S, Fouldrin G, Petit M, Frebourg T, Campion D. The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit. Molecular Psychiatry. 9: 320-2. PMID 14569275 DOI: 10.1038/Sj.Mp.4001443  1
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