| Year |
Citation |
Score |
| 2023 |
Habart M, Lio G, Soumier A, Demily C, Sirigu A. An optimized iDISCO+ protocol for tissue clearing and 3D analysis of oxytocin and vasopressin cell network in the developing mouse brain. Star Protocols. 4: 101968. PMID 36598854 DOI: 10.1016/j.xpro.2022.101968 |
0.471 |
|
| 2022 |
Gomez A, Lio G, Costa M, Sirigu A, Demily C. Dissociation of early and late face-related processes in autism spectrum disorder and Williams syndrome. Orphanet Journal of Rare Diseases. 17: 244. PMID 35733166 DOI: 10.1186/s13023-022-02395-6 |
0.55 |
|
| 2021 |
Soumier A, Habart M, Lio G, Demily C, Sirigu A. Differential fate between oxytocin and vasopressin cells in the developing mouse brain. Iscience. 25: 103655. PMID 35028535 DOI: 10.1016/j.isci.2021.103655 |
0.494 |
|
| 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 |
0.56 |
|
| 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 |
0.337 |
|
| 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 |
0.328 |
|
| 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 |
0.328 |
|
| 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 |
0.387 |
|
| 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 |
0.319 |
|
| 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 |
0.314 |
|
| 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 |
0.356 |
|
| 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 |
0.304 |
|
| 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 |
0.359 |
|
| 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 |
0.361 |
|
| 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 |
0.348 |
|
| 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 |
0.369 |
|
| 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 |
0.355 |
|
| 2017 |
Darmedru C, Demily C, Franck N. [Preventing violence in schizophrenia with cognitive remediation]. L'Encephale. 44: 158-167. PMID 28641817 DOI: 10.1016/J.Encep.2017.05.001 |
0.372 |
|
| 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 |
0.338 |
|
| 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 |
0.341 |
|
| 2017 |
Darmedru C, Demily C, Franck N. Cognitive remediation and social cognitive training for violence in schizophrenia: a systematic review. Psychiatry Research. 251: 266-274. PMID 28219026 DOI: 10.1016/J.Psychres.2016.12.062 |
0.328 |
|
| 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 |
0.37 |
|
| 2017 |
Peyroux E, Babinet MN, Demily C, Cannarsa C, Michael G. Social cognition in children with 22q11 deletion syndrome European Journal of Paediatric Neurology. 21: e141. DOI: 10.1016/J.Ejpn.2017.04.1284 |
0.329 |
|
| 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 |
0.344 |
|
| 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 |
0.31 |
|
| 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 |
0.396 |
|
| 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 |
0.392 |
|
| 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 |
0.329 |
|
| 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 |
0.334 |
|
| 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 |
0.317 |
|
| 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 |
0.343 |
|
| 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 |
0.369 |
|
| 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 |
0.337 |
|
| 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 |
0.308 |
|
| 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 |
0.352 |
|
| 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 |
0.36 |
|
| 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 |
0.335 |
|
| 2010 |
Demily C, Chouinard VA, Chouinard G. [Iatrogenic psychiatric-like symptoms recognition]. L'Encephale. 36: 417-24. PMID 21035632 DOI: 10.1016/J.Encep.2010.01.003 |
0.319 |
|
| 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 |
0.332 |
|
| 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 |
0.572 |
|
| 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 |
0.345 |
|
| 2008 |
Demily C, Jacquet P, Marie-Cardine M. [How to differentiate schizophrenia from bipolar disorder using cognitive assessment?]. L'Encephale. 35: 139-45. PMID 19393382 DOI: 10.1016/J.Encep.2008.03.011 |
0.427 |
|
| 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 |
0.335 |
|
| 2008 |
Cavezian C, Berquand-Merle M, Franck N, Demily C. 47 – Chess self-training for cognitive remediation in schizophrenia Schizophrenia Research. 98: 53. DOI: 10.1016/J.Schres.2007.12.114 |
0.31 |
|
| 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 |
0.558 |
|
| 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 |
0.34 |
|
| 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 |
0.707 |
|
| 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 |
0.713 |
|
| 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 |
0.657 |
|
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