1. Musio, Antonio. 2020. The multiple facets of the SMC1A gene. In Gene, 743, 144612. doi:10.1016/j.gene.2020.144612. https://pubmed.ncbi.nlm.nih.gov/32222533/
2. Di Nardo, Maddalena, Astigiano, Simonetta, Baldari, Silvia, Soddu, Silvia, Musio, Antonio. 2024. The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer. In Journal of experimental & clinical cancer research : CR, 43, 49. doi:10.1186/s13046-024-02976-2. https://pubmed.ncbi.nlm.nih.gov/38365745/
3. Ye, Y Z, Duan, J, Hu, Z Q, Liao, J X, Chen, L. . [Developmental and epileptic encephalopathy 85 caused by SMC1A gene truncating variation: 4 cases report and literature review]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 60, 583-587. doi:10.3760/cma.j.cn112140-20211126-00994. https://pubmed.ncbi.nlm.nih.gov/35658367/
4. Sarogni, Patrizia, Pallotta, Maria M, Musio, Antonio. 2019. Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach. In Journal of medical genetics, 57, 289-295. doi:10.1136/jmedgenet-2019-106277. https://pubmed.ncbi.nlm.nih.gov/31704779/
5. Bernardo, Pia, Cuccurullo, Claudia, Rubino, Marica, Bilo, Leonilda, Coppola, Antonietta. 2024. X-Linked Epilepsies: A Narrative Review. In International journal of molecular sciences, 25, . doi:10.3390/ijms25074110. https://pubmed.ncbi.nlm.nih.gov/38612920/
6. Gibellato, Elisabetta, Cianci, Paola, Mariani, Milena, Biondi, Andrea, Selicorni, Angelo. 2024. SMC1A epilepsy syndrome: clinical data from a large international cohort. In American journal of medical genetics. Part A, 194, e63577. doi:10.1002/ajmg.a.63577. https://pubmed.ncbi.nlm.nih.gov/38421079/
7. Kaur, Maninder, Blair, Justin, Devkota, Batsal, Raible, Sarah E, Krantz, Ian D. 2023. Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms. In American journal of medical genetics. Part A, 191, 2113-2131. doi:10.1002/ajmg.a.63247. https://pubmed.ncbi.nlm.nih.gov/37377026/