Cinzia Cameli
Overview
Explore the profile of Cinzia Cameli including associated specialties, affiliations and a list of published articles.
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15
Citations
158
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Recent Articles
1.
Viggiano M, Ceroni F, Visconti P, Posar A, Scaduto M, Sandoni L, et al.
NPJ Genom Med
. 2024 Mar;
9(1):21.
PMID: 38519481
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a strong genetic component in which rare variants contribute significantly to risk. We performed whole genome and/or exome sequencing (WGS...
2.
Bacchelli E, Viggiano M, Ceroni F, Visconti P, Posar A, Scaduto M, et al.
Res Sq
. 2023 Nov;
PMID: 37961520
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a strong genetic component in which rare variants contribute significantly to risk. We have performed whole genome and/or exome sequencing...
3.
Caporali L, Fiorini C, Palombo F, Romagnoli M, Baccari F, Zenesini C, et al.
Front Genet
. 2022 Nov;
13:953762.
PMID: 36419830
Autism spectrum disorder (ASD) is a clinically heterogeneous class of neurodevelopmental conditions with a strong, albeit complex, genetic basis. The genetic architecture of ASD includes different genetic models, from monogenic...
4.
Viggiano M, DAndrea T, Cameli C, Posar A, Visconti P, Scaduto M, et al.
Front Psychiatry
. 2022 Mar;
13:858238.
PMID: 35350424
Autism Spectrum Disorder (ASD) is a highly heterogeneous neuropsychiatric disorder with a strong genetic component. The genetic architecture is complex, consisting of a combination of common low-risk and more penetrant...
5.
Cameli C, Viggiano M, Rochat M, Maresca A, Caporali L, Fiorini C, et al.
J Cell Mol Med
. 2021 Jan;
25(5):2459-2470.
PMID: 33476483
Autism spectrum disorder (ASD) is characterized by a complex polygenic background, but with the unique feature of a subset of cases (~15%-30%) presenting a rare large-effect variant. However, clinical interpretation...
6.
Rochat M, Distefano G, Maffei M, Toni F, Posar A, Scaduto M, et al.
Brain Sci
. 2020 Oct;
10(10).
PMID: 33081247
We examined the potential benefits of neuroimaging measurements across the first 5 years of life in detecting early comorbid or etiological signs of autism spectrum disorder (ASD). In particular, we...
7.
Bacchelli E, Cameli C, Viggiano M, Igliozzi R, Mancini A, Tancredi R, et al.
Sci Rep
. 2020 Feb;
10(1):3198.
PMID: 32081867
Autism spectrum disorder (ASD) is a neurodevelopmental condition with a complex and heterogeneous genetic etiology. While a proportion of ASD risk is attributable to common variants, rare copy-number variants (CNVs)...
8.
Loi E, Moi L, Blois S, Bacchelli E, Vega Benedetti A, Cameli C, et al.
J Cell Mol Med
. 2019 Dec;
24(2):2064-2069.
PMID: 31800155
Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders characterized by high heritability. It is known that genetic factors contribute to ASD pathogenesis. In particular, copy number variants (CNVs)...
9.
Pippucci T, Licchetta L, Baldassari S, Marconi C, De Luise M, Myers C, et al.
Ann Clin Transl Neurol
. 2019 Mar;
6(3):475-485.
PMID: 30911571
Objective: We investigated the contribution to sporadic focal epilepsies (FE) of ultrarare variants in genes coding for the components of complexes regulating mechanistic Target Of Rapamycin (mTOR)complex 1 (mTORC1). Methods:...
10.
Bacchelli E, Loi E, Cameli C, Moi L, Vega-Benedetti A, Blois S, et al.
J Clin Med
. 2019 Feb;
8(2).
PMID: 30736458
Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders with high heritability, although their underlying genetic factors are still largely unknown. Here we present a comprehensive genetic characterization of...