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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 18, 2017
Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genesCarla Lintas, Chiara Picinelli, Ignazio Stefano Piras, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 28, 2016
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disordersChiara Picinelli, Carla Lintas, Ignazio Stefano Piras, et al.
Molecular Syndromology|March 22, 2016
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial FeaturesCarla Lintas, Chiara Picinelli, Ignazio S Piras, et al.
Molecular Genetics & Genomic Medicine|June 28, 2022
Yield of array-CGH analysis in Tunisian children with autism spectrum disorderFethia Chehbani, Pasquale Tomaiuolo, Chiara Picinelli, et al.
European Journal of Medical Genetics|January 15, 2013
Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotypeCristina Gervasini, Ilaria Parenti, Chiara Picinelli, et al.
Molecular Syndromology|February 9, 2019
An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic PatientCarla Lintas, Roberto Sacco, Claudio Tabolacci, et al.
Clinical Genetics|March 16, 2019
Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic reviewPaola Castronovo, Marco Baccarin, Arianna Ricciardello, et al.
BMC Medical Genetics|June 3, 2014
New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 geneMilena Crippa, Ilaria Bestetti, Mario Perotti, et al.
Genes, Brain, and Behavior|March 7, 2020
Appropriateness of array-CGH in the ADHD clinics: A comparative studyMarco Baccarin, Chiara Picinelli, Pasquale Tomaiuolo, et al.
Epigenetics|April 24, 2014
Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controlsIlaria Parenti, Davide Rovina, Maura Masciadri, et al.
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