Elena Maestrini
Affiliations: | Biology | Università di Bologna, Bologna, Italy |
Area:
Human GeneticsGoogle:
"Elena Maestrini"Parents
Sign in to add mentor| Orsetta Zuffardi | grad student | ||
| Anthony P. Monaco | research scientist | Oxford |
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Publications
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| Bacchelli E, Viggiano M, Ceroni F, et al. (2023) Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder. Research Square |
| Caporali L, Fiorini C, Palombo F, et al. (2022) Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder. Frontiers in Genetics. 13: 953762 |
| Viggiano M, D'Andrea T, Cameli C, et al. (2022) Contribution of Variants in Autism Spectrum Disorder Susceptibility. Frontiers in Psychiatry. 13: 858238 |
| Cameli C, Viggiano M, Rochat MJ, et al. (2021) An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. Journal of Cellular and Molecular Medicine |
| Lin BD, Colas F, Nijman IJ, et al. (2020) The role of rare compound heterozygous events in autism spectrum disorder. Translational Psychiatry. 10: 204 |
| Bacchelli E, Cameli C, Viggiano M, et al. (2020) An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific Reports. 10: 3198 |
| Loi E, Moi L, Blois S, et al. (2019) ELMOD3-SH2D6 gene fusion as a possible co-star actor in autism spectrum disorder scenario. Journal of Cellular and Molecular Medicine |
| Bacchelli E, Loi E, Cameli C, et al. (2019) Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies as a Functionally Relevant Candidate Gene. Journal of Clinical Medicine. 8 |
| Cameli C, Bacchelli E, De Paola M, et al. (2018) Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment. European Journal of Human Genetics : Ejhg |
| Anttila V, Bulik-Sullivan B, et al. (2018) Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360 |