Claudine Laurent-Levinson

Publications

Pré-publication, Document de travail (1)

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects Worrawat Engchuan,Omar Shanta,Kuldeep Kumar,Jeffrey R Macdonald,Bhooma Thiruvahindrapuramet al. 2025 Pré-publication, Document de travail inserm-05294360v1

Article dans une revue (16)

Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe – A multi-professional survey study Kati Koido,Charlotta Ingvoldstad Malmgren,Lejla Pojskic,Peter Z Almos,Sarah E Bergenet al. European Journal of Medical Genetics, 2023, 66 (8), pp.104805. ⟨10.1016/j.ejmg.2023.104805⟩ Article dans une revue inserm-04169323v1
Mapping genomic loci implicates genes and synaptic biology in schizophrenia Vassily Trubetskoy,Antonio Pardiñas,Ting Qi,Georgia Panagiotaropoulou,Swapnil Awasthiet al. Nature, 2022, 604 (7906), pp.502-508. ⟨10.1038/s41586-022-04434-5⟩ Article dans une revue hal-03864249v1
Narcolepsy and psychosis: A systematic review Cyril Hanin,Isabelle Arnulf,Jean‐baptiste Maranci,Michel Lecendreux,Douglas F Levinsonet al. Acta Psychiatrica Scandinavica, 2021, ⟨10.1111/acps.13300⟩ Article dans une revue hal-03233717v1
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Phil Lee,Verneri Anttila,Hyejung Won,Yen-Chen Feng,Jacob Rosenthalet al. Cell, 2019, 179 (7), pp.1469-1482.e11. ⟨10.1016/j.cell.2019.11.020⟩ Article dans une revue hal-04573676v1
Developmental and symptom profiles in early-onset psychosis Vladimir Ferrafiat,Marie Raffin,Elena Freri,Tiziana Granata,Nardo Nardocciet al. Schizophrenia Research, 2019, 93 (3), pp.567-576. ⟨10.1016/j.schres.2019.10.028⟩ Article dans une revue hal-02446602v1
1q21.1 microduplication: large verbal–nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number Jean Xavier,Bo Zhou,Frédéric Bilan,Xianglong Zhang,Brigitte Gilbert-Dussardieret al. npj Genomic Medicine, 2018, 3 (1), pp.24. ⟨10.1038/s41525-018-0059-2⟩ Article dans une revue hal-01974030v1
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia Russell L Mclaughlin,Dick Schijven,Wouter van Rheenen,Kristel R van Eijk,Margaret O’brienet al. Nature Communications, 2017, 8 (1), pp.14774. ⟨10.1038/ncomms14774⟩ Article dans une revue hal-04423266v1
An overview of medical risk factors for childhood psychosis: Implications for research and treatment Marianna Giannitelli,Angèle Consoli,Marie Raffin,Renaud Jardri,Douglas F. Levinsonet al. Schizophrenia Research, 2017, Schizophrenia Research, 192, pp.39-49. ⟨10.1016/j.schres.2017.05.011⟩ Article dans une revue hal-02533309v1
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Christian R Marshall,Daniel P Howrigan,Daniele Merico,Bhooma Thiruvahindrapuram,Wenting Wuet al. Nature Genetics, 2017, 49 (1), pp.27 - 35. ⟨10.1038/ng.3725⟩ Article dans une revue hal-04589228v1
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept Barbara Franke,Jason L Stein,Stephan Ripke,Verneri Anttila,Derrek P Hibaret al. Nature Neuroscience, 2016, 19 (3), pp.420 - 431. ⟨10.1038/nn.4228⟩ Article dans une revue hal-01382569v1
Facial, vocal and cross-modal emotion processing in early-onset schizophrenia spectrum disorders Marianna Giannitelli,Jean Xavier,Anne François,Nicolas Bodeau,Claudine Laurentet al. Schizophrenia Research, 2015, 168 (1-2), pp.252-259. ⟨10.1016/j.schres.2015.07.039⟩ Article dans une revue istex hal-02484424v1
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders Caroline Nava,Johanna Rupp,Jean-Paul Boissel,Cyril Mignot,Agnès Rastetteret al. Amino Acids, 2015, 47 (12), pp.2647-2658. ⟨10.1007/s00726-015-2057-3⟩ Article dans une revue hal-01191525v1
Association study in three different populations between the GPR 88 gene and major psychoses Maria del Zompo,Jean‐françois Deleuze,Caterina Chillotti,Emmanuelle Cousin,Dana Niehauset al. Molecular Genetics & Genomic Medicine, 2014, 2 (2), pp.152-159. ⟨10.1002/mgg3.54⟩ Article dans une revue hal-02989910v1
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? Claire Amiet,Isabelle Gourfinkel-An,Claudine Laurent,Nicolas Bodeau,Bérengère Géninet al. Molecular Autism, 2013, 4 (1), pp.47. ⟨10.1186/2040-2392-4-47⟩ Article dans une revue inserm-00918581v1
CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia Claudine Laurent,Dana Niehaus,Stéphanie Bauché,Douglas Levinson,Stéphane Soubigouet al. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2003, 116B (1), pp.45-50. ⟨10.1002/ajmg.b.10797⟩ Article dans une revue istex hal-03863965v1
No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample Douglas Levinson,Peter Holmans,Claudine Laurent,Brien Riley,Ann Pulveret al. Science, 2002, 296 (5568), pp.739-741. ⟨10.1126/science.1069914⟩ Article dans une revue hal-03863693v1