Claudine Laurent-Levinson
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Explore the profile of Claudine Laurent-Levinson including associated specialties, affiliations and a list of published articles.
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10
Citations
893
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Recent Articles
1.
Laurent-Levinson C, Pellen A, Pellerin H, Hanin C, Bouzy J, Devernay M, et al.
BJPsych Open
. 2024 Feb;
10(2):e47.
PMID: 38362905
Background: Previous pandemics have had negative effects on mental health, but there are few data on children and adolescents who were receiving ongoing psychiatric treatment. Aims: To study changes in...
2.
Dhossche D, de Billy C, Laurent-Levinson C, Le Normand M, Recasens C, Robel L, et al.
Front Psychiatry
. 2023 Oct;
14:1186555.
PMID: 37810596
Background: Individuals with Phelan-McDermid syndrome (PMS) present with a wide range of diagnoses: autism spectrum disorder, intellectual disability, or schizophrenia. Differences in the genetic background could explain these different neurodevelopmental...
3.
Koido K, Ingvoldstad Malmgren C, Pojskic L, Almos P, Bergen S, Borg I, et al.
Eur J Med Genet
. 2023 Jul;
66(8):104805.
PMID: 37406854
Genetic research has identified a large number of genetic variants, both rare and common, underlying neurodevelopmental disorders (NDD) and major psychiatric disorders. Currently, these findings are being translated into clinical...
4.
Liu D, Meyer D, Fennessy B, Feng C, Cheng E, Johnson J, et al.
Nat Genet
. 2023 Mar;
55(3):369-376.
PMID: 36914870
Schizophrenia (SCZ) is a chronic mental illness and among the most debilitating conditions encountered in medical practice. A recent landmark SCZ study of the protein-coding regions of the genome identified...
5.
Trubetskoy V, Pardinas A, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli T, et al.
Nature
. 2022 Apr;
604(7906):502-508.
PMID: 35396580
Schizophrenia has a heritability of 60-80%, much of which is attributable to common risk alleles. Here, in a two-stage genome-wide association study of up to 76,755 individuals with schizophrenia and...
6.
Hanin C, Arnulf I, Maranci J, Lecendreux M, Levinson D, Cohen D, et al.
Acta Psychiatr Scand
. 2021 Mar;
144(1):28-41.
PMID: 33779983
Objective: Narcolepsy is a rare sleep disorder in which psychotic-like symptoms can present diagnostic and therapeutic challenges. We aimed to review the association between, and medical management of, narcolepsy and...
7.
Giannitelli M, Levinson D, Cohen D, Xavier J, Laurent-Levinson C
Schizophr Res
. 2019 Dec;
216:470-478.
PMID: 31874744
Psychotic disorders in children are more heterogeneous than is captured by categorical diagnoses. In a new cohort of children and adolescents, we evaluated the relationships among age at onset (AAO),...
8.
Xavier J, Zhou B, Bilan F, Zhang X, Gilbert-Dussardier B, Viaux-Savelon S, et al.
NPJ Genom Med
. 2018 Aug;
3:24.
PMID: 30155272
Microduplication of chromosome 1q21.1 is observed in ~0.03% of adults. It has a highly variable, incompletely penetrant phenotype that can include intellectual disability, global developmental delay, specific learning disabilities, autism,...
9.
Raffin M, Consoli A, Giannitelli M, Philippe A, Keren B, Bodeau N, et al.
J Am Acad Child Adolesc Psychiatry
. 2018 Jul;
57(7):518-525.e1.
PMID: 29960699
Pediatric catatonia is a rare and severe neuropsychiatric syndrome. We previously reported, in 58 children and adolescents with catatonia, a high prevalence (up to 20%) of medical conditions, some of...
10.
An overview of medical risk factors for childhood psychosis: Implications for research and treatment
Giannitelli M, Consoli A, Raffin M, Jardri R, Levinson D, Cohen D, et al.
Schizophr Res
. 2017 May;
192:39-49.
PMID: 28526280
Objective: Psychotic disorders in childhood and early adolescence often progress to chronic schizophrenia, but in many cases there are diagnosable medical and genetic causes or risk factors. We reviewed our...