Caroline Demily
Affiliations: | Universite Lyon 1, Villeurbanne, Auvergne-Rhône-Alpes, France |
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Parents
Sign in to add mentor| Dominique Campion | grad student | 2009 | Universite Lyon 1 | |
| (Génétique et cognition sociale dans la schizophrénie) | ||||
| Angela Sirigu | grad student | 2009 | Universite Lyon 1 | |
| (Génétique et cognition sociale dans la schizophrénie) | ||||
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Publications
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| Habart M, Lio G, Soumier A, et al. (2023) 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 |
| Gomez A, Lio G, Costa M, et al. (2022) Dissociation of early and late face-related processes in autism spectrum disorder and Williams syndrome. Orphanet Journal of Rare Diseases. 17: 244 |
| Soumier A, Habart M, Lio G, et al. (2021) Differential fate between oxytocin and vasopressin cells in the developing mouse brain. Iscience. 25: 103655 |
| Gomez A, Costa M, Lio G, et al. (2020) 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 |
| Poisson A, Chatron N, Labalme A, et al. (2020) Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report. Bmc Medical Genetics. 21: 10 |
| Favre E, Leleu A, Peyroux E, et al. (2019) Exploratory case study of monozygotic twins with 22q11.2DS provides further clues to circumscribe neurocognitive markers of psychotic symptoms. Neuroimage. Clinical. 24: 101987 |
| Munnich A, Demily C, Frugère L, et al. (2019) Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder. Molecular Autism. 10: 33 |
| Masson J, Demily C, Chatron N, et al. (2019) 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 |
| Peyroux E, Babinet MN, Cannarsa C, et al. (2019) 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 |
| Demily C, Duwime C, Lopez C, et al. (2019) Corpus callosum metrics predict severity of visuospatial and neuromotor dysfuntions in ARID1B mutations with Coffin-Siris syndrome. Psychiatric Genetics |