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Author

Cinzia Cameli

Observed name: Cameli, Cinzia
Observed institution: University of Bologna
ORCID: 0000-0003-2856-0686
Observed ORCID: 0000-0003-2856-0686
OpenAlex ID: A5060524331
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray
2020 · Elena Bacchelli, Cinzia Cameli, et al. · Scientific Reports · 63
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A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants
2016 · Elena Bacchelli, Maria Michela Cainazzo, et al. · The Journal of Headache and Pain · 61
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Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility
2015 · Elena Bacchelli, Agatino Battaglia, et al. · American Journal of Medical Genetics Part A · 56
Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies CAPG as a Functionally Relevant Candidate Gene
2019 · Elena Bacchelli, Eleonora Loi, et al. · Journal of Clinical Medicine · 47
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Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas
2018 · Manila Antonelli, Antonio Fadda, et al. · Oncotarget · 28
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Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
2024 · Marta Viggiano, Fabiola Ceroni, et al. · npj Genomic Medicine · 27
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Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies
2019 · Tommaso Pippucci, Laura Licchetta, et al. · Annals of Clinical and Translational Neurology · 25
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Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment
2018 · Cinzia Cameli, Elena Bacchelli, et al. · European Journal of Human Genetics · 22
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Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old
2020 · Magali Jane Rochat, Giacomo Distefano, et al. · Brain Sciences · 20
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Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility
2022 · Marta Viggiano, Tiziano D'Andrea, et al. · Frontiers in Psychiatry · 14
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ELMOD3 ‐ SH2D6 gene fusion as a possible co‐star actor in autism spectrum disorder scenario
2019 · Eleonora Loi, Loredana Moi, et al. · Journal of Cellular and Molecular Medicine · 14
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Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder
2022 · Leonardo Caporali, Claudio Fiorini, et al. · Frontiers in Genetics · 9
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
2021 · Cinzia Cameli, Marta Viggiano, et al. · Journal of Cellular and Molecular Medicine · 9
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O015. Evaluation of the genetic polymorphism of the α3 (CHRNA3) and α5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache
2015 · Maria Michela Cainazzo, Ilaria Tiraferri, et al. · The Journal of Headache and Pain · 4
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Identification of a rare deletion encompassing ELMOD3 and CAPG in two siblings with Autism Spectrum Disorder
2015 · Elena Bacchelli, Loredana Moi, et al. · UNICA IRIS Institutional Research Information System (University of Cagliari) · 1
Investigation of genetic risk variants for nicotine dependence and cluster headache
2018 · Cameli, Cinzia · AMS Dottorato Institutional Doctoral Theses Repository (University of Bologna)
Additional file 1: of A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants
2016 · Bacchelli, Elena, Cainazzo, Maria, et al. · Figshare
Works count: 18
Citation count: 400
H-index: 11
I10-index: 11
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