Roberto Ciccone

4.6k total citations
51 papers, 1.4k citations indexed

About

Roberto Ciccone is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Roberto Ciccone has authored 51 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 28 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Roberto Ciccone's work include Genomic variations and chromosomal abnormalities (31 papers), Chromosomal and Genetic Variations (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Roberto Ciccone is often cited by papers focused on Genomic variations and chromosomal abnormalities (31 papers), Chromosomal and Genetic Variations (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Roberto Ciccone collaborates with scholars based in Italy, United Kingdom and United States. Roberto Ciccone's co-authors include Orsetta Zuffardi, Roberto Giorda, María Clara Bonaglia, Annalisa Vetro, Erika Della Mina, Elena Rossi, Francesca Novara, Maria Grazia Patricelli, Tiziano Pramparo and Conny van Ravenswaaij and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Nephrology Dialysis Transplantation.

In The Last Decade

Roberto Ciccone

50 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Roberto Ciccone Italy 23 956 681 283 270 102 51 1.4k
Maria Isabel Melaragno Brazil 20 893 0.9× 592 0.9× 221 0.8× 270 1.0× 94 0.9× 117 1.3k
Zhishuo Ou United States 14 862 0.9× 602 0.9× 230 0.8× 214 0.8× 80 0.8× 26 1.1k
Stefania Gimelli Switzerland 21 900 0.9× 787 1.2× 228 0.8× 225 0.8× 174 1.7× 64 1.6k
Lionel Willatt United Kingdom 22 1.3k 1.3× 909 1.3× 328 1.2× 260 1.0× 89 0.9× 30 1.8k
Teresa Mattina Italy 18 839 0.9× 764 1.1× 181 0.6× 172 0.6× 101 1.0× 59 1.4k
Evica Rajcan‐Separovic Canada 24 770 0.8× 775 1.1× 386 1.4× 178 0.7× 66 0.6× 58 1.6k
Emmanuelle Lemyre Canada 22 879 0.9× 550 0.8× 276 1.0× 95 0.4× 129 1.3× 52 1.3k
Ewa Obersztyn Poland 19 711 0.7× 692 1.0× 130 0.5× 170 0.6× 84 0.8× 78 1.2k
Sung‐Hae Kang United States 20 925 1.0× 737 1.1× 348 1.2× 180 0.7× 153 1.5× 30 1.4k
Katrin Õunap Estonia 25 857 0.9× 1.0k 1.5× 264 0.9× 103 0.4× 75 0.7× 106 1.8k

Countries citing papers authored by Roberto Ciccone

Since Specialization
Citations

This map shows the geographic impact of Roberto Ciccone's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Roberto Ciccone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Ciccone more than expected).

Fields of papers citing papers by Roberto Ciccone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roberto Ciccone. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Roberto Ciccone. The network helps show where Roberto Ciccone may publish in the future.

Co-authorship network of co-authors of Roberto Ciccone

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Ciccone. A scholar is included among the top collaborators of Roberto Ciccone based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Roberto Ciccone. Roberto Ciccone is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zanni, Ginevra, Francesco Nicita, Simona Cascioli, et al.. (2021). PIGQ-Related Glycophosphatidylinositol Deficiency Associated with Nonprogressive Congenital Ataxia. The Cerebellum. 21(4). 525–530. 4 indexed citations
2.
Peron, Angela, Francesca Novara, Francesca La Briola, et al.. (2020). Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype. American Journal of Medical Genetics Part A. 182(4). 823–828. 11 indexed citations
3.
Manai, Federico, Roberto Ciccone, Francesca Novara, et al.. (2020). The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma. Cancer Genomics & Proteomics. 17(2). 117–130. 7 indexed citations
4.
Novara, Francesca, Alessandro Simonati, Federico Sicca, et al.. (2014). MECP2 duplication phenotype in symptomatic females: report of three further cases. Molecular Cytogenetics. 7(1). 10–10. 19 indexed citations
5.
Piazza, Elena, Erika Della Mina, Ivan Limongelli, et al.. (2013). Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene. European Journal of Medical Genetics. 56(10). 551–555. 10 indexed citations
6.
Novara, Francesca, Enrico Alfei, Stefano D’Arrigo, et al.. (2012). 5p13 microduplication syndrome: A new case and better clinical definition of the syndrome. European Journal of Medical Genetics. 56(1). 54–58. 24 indexed citations
7.
Iascone, Maria, Roberto Ciccone, Lorenzo Galletti, et al.. (2011). Identification of de novo mutations and rare variants in hypoplastic left heart syndrome. Clinical Genetics. 81(6). 542–554. 81 indexed citations
8.
Giorda, Roberto, Silvana Beri, María Clara Bonaglia, et al.. (2011). Common structural features characterize interstitial intrachromosomal Xp and 18q triplications. American Journal of Medical Genetics Part A. 155(11). 2681–2687. 6 indexed citations
9.
Wischmeijer, Anita, Pamela Magini, Roberto Giorda, et al.. (2010). Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. Molecular Syndromology. 1(4). 176–184. 23 indexed citations
10.
Sironi, Francesca, Luca Trotta, Angelo Antonini, et al.. (2009). α-Synuclein multiplication analysis in Italian familial Parkinson disease. Parkinsonism & Related Disorders. 16(3). 228–231. 27 indexed citations
11.
Zuffardi, Orsetta, María Clara Bonaglia, Roberto Ciccone, & Roberto Giorda. (2009). Inverted duplications deletions: underdiagnosed rearrangements??. Clinical Genetics. 75(6). 505–513. 68 indexed citations
12.
Bonaglia, María Clara, Roberto Ciccone, Giorgio Gimelli, et al.. (2008). Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype. European Journal of Human Genetics. 16(12). 1443–1449. 75 indexed citations
13.
Rossi, Elena, Anna Verri, Maria Grazia Patricelli, et al.. (2008). A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea. European Journal of Medical Genetics. 51(6). 631–638. 59 indexed citations
14.
Pramparo, Tiziano, Manuela De Gregori, Stefania Gimelli, et al.. (2008). A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation. American Journal of Medical Genetics Part A. 146A(13). 1754–1760. 19 indexed citations
15.
Clayton‐Smith, Jill, Sarah Walters, Emma Hobson, et al.. (2008). Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance. European Journal of Human Genetics. 17(4). 434–443. 64 indexed citations
16.
Bonaglia, María Clara, et al.. (2008). A familial inverted duplication/deletion of 2p25.1–25.3 provides new clues on the genesis of inverted duplications. European Journal of Human Genetics. 17(2). 179–186. 32 indexed citations
17.
Wieland, Ilse, Carola I. Weidner, Roberto Ciccone, et al.. (2007). Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. Clinical Genetics. 72(6). 506–516. 32 indexed citations
18.
Giorda, Roberto, Roberto Ciccone, Giorgio Gimelli, et al.. (2007). Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Human Mutation. 28(5). 459–468. 37 indexed citations
19.
Priolo, Manuela, et al.. (2006). Malpuech syndrome: Broadening the clinical spectrum and molecular analysis by array-CGH. European Journal of Medical Genetics. 50(2). 139–143. 4 indexed citations
20.
Cau, Milena, Maria Addis, Rita Congiu, et al.. (2006). A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome. Journal of Human Genetics. 51(11). 1030–1036. 22 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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