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Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675.
Sciacca FL, Rizzo A, Bedini G, Capone F, Di Lazzaro V, Nava S, Acerbi F, Rossi Sebastiano D, Binelli S, Faragò G, Gioppo A, Grisoli M, Bruzzone MG, Ferroli P, Pantaleoni C, Caputi L, Gomez JV, Parati EA, Bersano A. Sciacca FL, et al. Int J Mol Sci. 2019 Dec 18;21(1):20. doi: 10.3390/ijms21010020. Int J Mol Sci. 2019. PMID: 31861461 Free PMC article.
CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder.
Annunziata S, Bulgheroni S, D'Arrigo S, Esposito S, Taddei M, Saletti V, Alfei E, Sciacca FL, Rizzo A, Pantaleoni C, Riva D. Annunziata S, et al. Among authors: sciacca fl. J Autism Dev Disord. 2023 Feb;53(2):615-623. doi: 10.1007/s10803-020-04833-5. Epub 2021 Jan 4. J Autism Dev Disord. 2023. PMID: 33394245
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.
Rizzo A, Alfei E, Zibordi F, Saletti V, Zorzi G, Freri E, Estienne M, Girgenti V, D'Arrigo S, Esposito S, Buldrini B, Moroni I, Milani D, Granata T, Ardissone A, Eoli M, Molteni B, Bigoni S, Pantaleoni C, Nardocci N, Sciacca FL. Rizzo A, et al. Among authors: sciacca fl. Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):557-562. doi: 10.1002/ajmg.b.32649. Epub 2018 Aug 14. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 30105822