Publications by authors named "Caroline Demily"

49Publications

Face first impression of trustworthiness in Williams Syndrome: Dissociating automatic vs decision based perception.

Cortex 2020 Aug 24;132:99-112. Epub 2020 Aug 24.

Univ Lyon, Centre National de la Recherche Scientifique, Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, F-69500, Lyon, France; Reference Center for Rare Diseases with Psychiatric Phenotype Génopsy, le Vinatier Hospital, Bron, France. Electronic address:

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http://dx.doi.org/10.1016/j.cortex.2020.07.015DOI Listing
August 2020

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.

BMC Med Genet 2020 01 8;21(1):10. Epub 2020 Jan 8.

Institut Neuromyogène, métabolisme énergétique et développement durable, CNRS UMR 5310, INSERM U1217, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

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http://dx.doi.org/10.1186/s12881-019-0946-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950831PMC
January 2020

[Twenty years of on-site clinical genetics consultations for people with ASD].

Med Sci (Paris) 2019 Nov 17;35(11):843-851. Epub 2019 Dec 17.

Fédération de Génétique Médicale et Institute Imagine, UMR Inserm 1163, Université Paris-Descartes, Hôpital Necker Enfants-Malades et Fondation Elan Retrouvé, 149 rue de Sèvres, 75015 Paris, France.

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http://dx.doi.org/10.1051/medsci/2019170DOI Listing
November 2019

The psychopharmacology of Wilson disease and other metabolic disorders.

Handb Clin Neurol 2019 ;165:191-205

Reference Center for Rare Disease, GénoPsy, Centre Hospitalier le Vinatier and Centre de Neuroscience Cognitive, Lyon, France. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-64012-3.00011-3DOI Listing
April 2020

Exploratory case study of monozygotic twins with 22q11.2DS provides further clues to circumscribe neurocognitive markers of psychotic symptoms.

Neuroimage Clin 2019 17;24:101987. Epub 2019 Aug 17.

GénoPsy, Centre de Référence Maladies Rares à Expression Psychiatrique, Centre Hospitalier Le Vinatier, 95 bd Pinel BP300.91, F-69 678 BRON Cedex, France; Equipe EDR-Psy, Institut de Sciences Cognitives Marc Jeannerod, CNRS-UMR5229 & Université Lyon 1 Claude Bernard, 67 bd Pinel, F-69 500 BRON, France. Electronic address:

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http://dx.doi.org/10.1016/j.nicl.2019.101987DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713843PMC
September 2020

Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.

Int J Mol Sci 2019 Jul 19;20(14). Epub 2019 Jul 19.

GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Centre Hospitalier le Vinatier and EDR-Psy Q19 Team (Centre National de la Recherche Scientifique & Lyon 1 Claude Bernard University), 69678 Bron, France.

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http://dx.doi.org/10.3390/ijms20143533DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679101PMC
July 2019

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome.

Transl Psychiatry 2019 02 4;9(1):67. Epub 2019 Feb 4.

Reference Center for Rare Diseases with Psychiatric Phenotype - GénoPsy, Centre Hospitalier le Vinatier, Marc Jeannerod Institute (CNRS & Claude Bernard Lyon 1 University), Bron, France.

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http://dx.doi.org/10.1038/s41398-019-0411-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362075PMC
February 2019

Satisfaction and Needs in Serious Mental Illness and Autism Spectrum Disorder: The REHABase Psychosocial Rehabilitation Project.

Psychiatr Serv 2019 04 29;70(4):316-323. Epub 2019 Jan 29.

Centre Ressource de Réhabilitation Psychosociale et de Remédiation Cognitive (CRR), Hôpital Le Vinatier, Centre National de la Recherche Scientifique (CNRS) et Université de Lyon, Lyon, France (Franck, Bon, Dekerle, Plasse, Cervello); Centre Référent Lyonnais de Réhabilitation Psychosociale (CL3R), Centre Hospitalier Le Vinatier, Lyon (Franck, Martin); REHALise, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne, France (Massoubre, Pommier); Centre Référent de Réhabilitation Psychosociale de Limoges (C2RL), Limoges, France (Legros-Lafarge); CREATIV & URC Pierre Deniker, Centre Hospitalier Laborit, Poitiers, France (Jaafari, Guillard-Bouhet); Centre Référent de Réhabilitation Psychosociale (C2RP), Centre Hospitalier Charles Perrens, Pôle Universitaire de Psychiatrie Adulte, Bordeaux, France (Quilès, Verdoux); Centre Référent de Réhabilitation Psychosociale (C2RP), Pôle De Réhabilitation Psychosociale, Bruges, France (Couhet); Centre Référent de Réhabilitation Psychosociale (C3R), Centre Hospitalier Alpes Isère, Grenoble, France (Gouache, Dubreucq); Centre de Référence Maladies Rares Génopsy, Centre Hospitalier Le Vinatier, CNRS et Université de Lyon, Lyon (Demily).

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http://dx.doi.org/10.1176/appi.ps.201800420DOI Listing
April 2019

12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome.

Eur J Med Genet 2019 Nov 30;62(11):103565. Epub 2018 Oct 30.

Hospices Civils de Lyon, Genetic Department and National HHT Reference Center, Femme-Mère-Enfants Hospital, Bron, F-69677, France.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212183055
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http://dx.doi.org/10.1016/j.ejmg.2018.10.017DOI Listing
November 2019

Regressive Autism Spectrum Disorder Expands the Phenotype of BSCL2/Seipin-Associated Neurodegeneration.

Biol Psychiatry 2019 02 24;85(4):e17-e19. Epub 2018 Aug 24.

GENDEV, Centre de Recherche en Neurosciences de Lyon, UMR 529, Centre National de la Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale U1028, Université Claude Bernard Lyon 1, Lyon, France; HCL, Department of Genetics, Reference Center for Developmental Anomalies and Malformation Syndromes, Oullins, France.

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https://linkinghub.elsevier.com/retrieve/pii/S00063223183152
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http://dx.doi.org/10.1016/j.biopsych.2018.05.010DOI Listing
February 2019

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 2018 07 20;18(1):235. Epub 2018 Jul 20.

GenoPsy, Reference center for rare diseases with psychiatric symptoms, Centre Hospitalier le Vinatier and EDR-Psy team (CNRS UMR 5229 & Lyon 1 University), 69678 BRON Cedex Lyon, Lyon, France.

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https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12
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http://dx.doi.org/10.1186/s12888-018-1810-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053752PMC
July 2018

Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype.

Front Pediatr 2018 3;6:102. Epub 2018 May 3.

Reference Center for Rare Diseases GénoPsy, CH Le Vinatier, UMR 5229, Université Lyon 1, CNRS, Lyon, France.

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http://journal.frontiersin.org/article/10.3389/fped.2018.001
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http://dx.doi.org/10.3389/fped.2018.00102DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943552PMC
May 2018

Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?

J Autism Dev Disord 2018 08;48(8):2886-2889

Département de génétique médicale, Institut Imagine, Hôpital Necker-Enfants Malades, INSERM UMR 1163, Université Paris Descartes-Sorbonne, Paris, France.

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http://dx.doi.org/10.1007/s10803-018-3552-7DOI Listing
August 2018

Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia.

Early Interv Psychiatry 2019 Apr 25;13(2):304-307. Epub 2018 Mar 25.

GénoPsy, Reference Center for Rare Diseases, Le Vinatier Hospital, Bron, France.

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http://dx.doi.org/10.1111/eip.12557DOI Listing
April 2019

Weight loss induced by quetiapine in a 22q11.2DS patient.

Mol Genet Metab Rep 2017 Dec 17;13:95-96. Epub 2017 Oct 17.

Centre ressource de réhabilitation psychosociale et de remédiation cognitive, CH Le Vinatier et UMR 5229 (CNRS and Université Lyon 1), Bron, France.

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http://dx.doi.org/10.1016/j.ymgmr.2017.10.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645303PMC
December 2017

Clinical and molecular cytogenetic characterization of four unrelated patients carrying 2p14 microdeletions.

Am J Med Genet A 2017 Aug 9;173(8):2268-2274. Epub 2017 Jun 9.

Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, Bron, France.

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http://dx.doi.org/10.1002/ajmg.a.38307DOI Listing
August 2017

Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary study.

Ann Gen Psychiatry 2017 4;16:19. Epub 2017 Apr 4.

Laboratory of Inherited Metabolic Diseases, Centre de Biologie Est, Hospices Civils de Lyon, Bron, France.

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http://dx.doi.org/10.1186/s12991-017-0142-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379609PMC
April 2017

Social cognition in Wilson's disease: A new phenotype?

PLoS One 2017 6;12(4):e0173467. Epub 2017 Apr 6.

Genopsy-Center for the Diagnosis and Management of Genetic Psychiatric Disorders, Le Vinatier Hospital, Lyon, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0173467PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383022PMC
September 2017

Evidence for dopaminergic denervation in classical galactosemia.

Mov Disord 2017 06 3;32(6):940-942. Epub 2017 Apr 3.

Université de Lyon, Université Lyon 1, Faculté de Médecine et de maïeutique Lyon Sud Charles Mérieux, Lyon, France.

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http://dx.doi.org/10.1002/mds.26980DOI Listing
June 2017

Authors' reply - Clozapine for mitochondrial psychosis.

Mol Genet Metab Rep 2017 Mar 6;10:101. Epub 2017 Feb 6.

INSERM UMR 1163, Université Paris Descartes-Sorbonne, Service de génétique clinique, Institut Imagine, Hôpital Necker-Enfants Malades, Paris, France.

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http://dx.doi.org/10.1016/j.ymgmr.2017.01.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295507PMC
March 2017

Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.

BMC Med Genet 2017 Jan 31;18(1). Epub 2017 Jan 31.

Centre de référence des anomalies du développement, Service de génétique, Hospices Civils de Lyon, & Centre de Recherche en Neurosciences de Lyon, Inserm U1028, UMR CNRS 5292, GENDEV Team, Lyon 1-Claude Bernard University, Bron, France.

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http://bmcmedgenet.biomedcentral.com/articles/10.1186/s12881
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http://dx.doi.org/10.1186/s12881-017-0371-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282903PMC
January 2017

Low dose clozapine controls adult-onset psychosis associated with the neurogenic ataxia-retinitis pigmentosa (NARP) mutation.

Mol Genet Metab Rep 2017 Mar 13;10:20-22. Epub 2016 Dec 13.

INSERM UMR 1163, Université Paris Descartes-Sorbonne, Service de génétique clinique, Institut Imagine, Hôpital Necker-Enfants Malades, Paris, France.

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http://dx.doi.org/10.1016/j.ymgmr.2016.12.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5157794PMC
March 2017

Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia?

Psychiatry Res 2016 Dec 27;246:738-744. Epub 2016 Oct 27.

Dept of Psychiatry, University Hospital Cochin (Site Tarnier), University Sorbonne-Paris Cité(Faculty of Medicine Paris Descartes), INSERM U 894, CPN, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.psychres.2016.07.066DOI Listing
December 2016

From High Intellectual Potential to Asperger Syndrome: Evidence for Differences and a Fundamental Overlap-A Systematic Review.

Front Psychol 2016 20;7:1605. Epub 2016 Oct 20.

Paris Descartes University, Sorbonne Paris CitéParis, France; Institut National de la Santé et de la Recherche Médicale UMR 1018-CESP, Paris-Saclay-Paris Sud University, UVSQParis, France; Child Psychiatry Department, Necker-Enfants Malades University HospitalParis, France; Department of Paediatrics, Child Development, Cochin-Port Royal University HospitalParis, France; IMAGINE Institute, Necker-Enfants Malades University HospitalParis, France.

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http://dx.doi.org/10.3389/fpsyg.2016.01605DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071629PMC
October 2016

Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia?

Eur J Med Genet 2016 Nov 14;59(11):596-603. Epub 2016 Sep 14.

Centre ressource de réhabilitation et de remédiation cognitive, SUR-CL3R, Centre Hospitalier le Vinatier et Centre de Neuroscience Cognitive, UMR 5229 (CNRS et Université Claude Bernard Lyon 1), Université de Lyon, Lyon, France.

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http://dx.doi.org/10.1016/j.ejmg.2016.09.007DOI Listing
November 2016

«Cognitus & Moi»: A Computer-Based Cognitive Remediation Program for Children with Intellectual Disability.

Front Psychiatry 2016 3;7:10. Epub 2016 Feb 3.

UMR 5229, EDR-Psy, Center of Cognitive Neuroscience, CNRS, University Lyon 1, Lyon, France; Centre référent lyonnais en réhabilitation psychosociale et en remédiation cognitive (CL3R), CH Le Vinatier, Bron, France.

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http://dx.doi.org/10.3389/fpsyt.2016.00010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737901PMC
February 2016

The Odor Context Facilitates the Perception of Low-Intensity Facial Expressions of Emotion.

PLoS One 2015 21;10(9):e0138656. Epub 2015 Sep 21.

Équipe Éthologie développementale et psychologie cognitive, Centre des Sciences du Goût et de l'Alimentation, UMR 6265 CNRS-UMR 1324 INRA-Université Bourgogne-Franche-Comté, Dijon, France; Institut Universitaire de France, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0138656PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577100PMC
May 2016

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.

Orphanet J Rare Dis 2015 Sep 4;10:111. Epub 2015 Sep 4.

Center for Screening and Treatment of Psychiatric Disorders of Genetic Origin, Vinatier Hospital, 95 Bd Pinel, 69678, Lyon, France.

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http://dx.doi.org/10.1186/s13023-015-0330-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559928PMC
September 2015

Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.

Eur Child Adolesc Psychiatry 2016 Mar 7;25(3):297-310. Epub 2015 Jul 7.

Centre de dépistage et de prises en charge des troubles psychiatriques d'origine génétique, Centre Hospitalier Le Vinatier, BP 30039, 95 Boulevard Pinel, 69678, Bron Cedex, France.

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http://dx.doi.org/10.1007/s00787-015-0741-1DOI Listing
March 2016

[Improving functional outcome of schizophrenia with cognitive remediation].

Presse Med 2015 Mar 24;44(3):292-7. Epub 2014 Dec 24.

Centre hospitalier Le Vinatier, 69677 Bron cedex, France.

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http://dx.doi.org/10.1016/j.lpm.2014.06.031DOI Listing
March 2015

Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.

BMC Med Genet 2014 Dec 11;15:132. Epub 2014 Dec 11.

Hospices Civils de Lyon, service de génétique et centre de référence des anomalies du développement, GHE, Lyon, France.

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http://dx.doi.org/10.1186/s12881-014-0132-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411819PMC
December 2014

Psychiatric manifestations of treatable hereditary metabolic disorders in adults.

Ann Gen Psychiatry 2014 24;13:27. Epub 2014 Sep 24.

Federation for Diseases of the Nervous System, Reference Centre for Lysosomal Diseases, Hospital Pitié Salpêtrière, Paris 75013, France.

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http://dx.doi.org/10.1186/s12991-014-0027-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255667PMC
December 2014

Cognitive remediation therapy (CRT) benefits more to patients with schizophrenia with low initial memory performances.

Disabil Rehabil 2015 11;37(10):846-53. Epub 2014 Aug 11.

Centre Référent en Remédiation et Réhabilitation Psychosociale (C3R-P) (SHU, Secteur 17), Inserm U894, Hôpital Sainte-Anne , Paris , France .

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http://dx.doi.org/10.3109/09638288.2014.946153DOI Listing
December 2015

Delusions and metacognition in patients with schizophrenia.

Cogn Neuropsychiatry 2012 28;17(1):1-18. Epub 2011 Jun 28.

Institut Jean-Nicod (CNRS and Ecole Normale Supérieure), Paris, France. nicolas.bruno@sat

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http://dx.doi.org/10.1080/13546805.2011.562071DOI Listing
April 2012

Recognition of self-generated facial emotions is impaired in schizophrenia.

J Neuropsychiatry Clin Neurosci 2011 ;23(2):189-93

Center for Cognitive Neuroscience, UMR 5229 (CNRS & Université Lyon 1), Bron, France.

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http://dx.doi.org/10.1176/jnp.23.2.jnp189DOI Listing
September 2011

Cognitive remediation: a promising tool for the treatment of schizophrenia.

Expert Rev Neurother 2008 Jul;8(7):1029-36

Université Lyon 1, Centre Hospitalier le Vinatier & Centre de Neuroscience Cognitive (CNRS UMR 5229), 67 Blvd Pinel 69675 Bron cedex, France.

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http://dx.doi.org/10.1586/14737175.8.7.1029DOI Listing
July 2008

No pathogenic rearrangement within the DISC 1 gene in psychosis.

Am J Med Genet B Neuropsychiatr Genet 2009 Jan;150B(1):148-50

INSERM U, IFRMP, Rouen, France.

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http://dx.doi.org/10.1002/ajmg.b.30753DOI Listing
January 2009

Gabapentin for ultra resistant schizophrenia with aggressive behavior.

Schizophr Res 2008 Mar 5;100(1-3):349-50. Epub 2008 Feb 5.

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http://dx.doi.org/10.1016/j.schres.2007.12.482DOI Listing
March 2008

Brain-derived neurotrophic factor in schizophrenia and its relation with dopamine.

Int Rev Neurobiol 2007 ;78:377-95

Unité de Psychiatrie, UFR de Médecine et de Pharmacie de Rouen, France.

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http://dx.doi.org/10.1016/S0074-7742(06)78012-6DOI Listing
November 2009

Treatment of cognitive dysfunction in schizophrenia.

Clin Ther 2005 ;27 Suppl A:S25-37

Department of Psychiatry, University Center St. Jozef, Kortenberg, Belgium.

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http://dx.doi.org/10.1016/j.clinthera.2005.07.015DOI Listing
October 2005