Nicola Chiarelli

1.4k total citations
40 papers, 1.0k citations indexed

About

Nicola Chiarelli is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Nicola Chiarelli has authored 40 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 21 papers in Molecular Biology and 8 papers in Cell Biology. Recurrent topics in Nicola Chiarelli's work include Connective tissue disorders research (34 papers), Dermatological and Skeletal Disorders (20 papers) and Bone health and treatments (5 papers). Nicola Chiarelli is often cited by papers focused on Connective tissue disorders research (34 papers), Dermatological and Skeletal Disorders (20 papers) and Bone health and treatments (5 papers). Nicola Chiarelli collaborates with scholars based in Italy, United States and Lebanon. Nicola Chiarelli's co-authors include Marco Ritelli, Marina Colombi, Nicoletta Zoppi, Marina Venturini, Chiara Dordoni, Piergiacomo Calzavara‐Pinton, Valeria Cinquina, Marco Castori, Giulia Carini and Silvia Morlino and has published in prestigious journals such as PLoS ONE, Neurology and FEBS Letters.

In The Last Decade

Nicola Chiarelli

40 papers receiving 987 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicola Chiarelli Italy 22 724 340 178 158 124 40 1.0k
Brad Angle United States 18 527 0.7× 444 1.3× 103 0.6× 191 1.2× 81 0.7× 33 1000
Gary S. Gottesman United States 20 394 0.5× 542 1.6× 451 2.5× 132 0.8× 209 1.7× 55 1.6k
Takuo Kubota Japan 19 404 0.6× 725 2.1× 268 1.5× 149 0.9× 292 2.4× 86 1.5k
Caroline Michot France 16 436 0.6× 395 1.2× 144 0.8× 89 0.6× 109 0.9× 43 823
Amina F. Zebboudj United States 7 164 0.2× 270 0.8× 169 0.9× 81 0.5× 58 0.5× 7 753
Adriano Angioni Italy 21 435 0.6× 739 2.2× 37 0.2× 176 1.1× 120 1.0× 56 1.3k
Francesca Crosti Italy 14 195 0.3× 278 0.8× 90 0.5× 96 0.6× 73 0.6× 40 884
Håkan Hedstrand Sweden 12 371 0.5× 359 1.1× 79 0.4× 291 1.8× 80 0.6× 14 1.4k
Christina L. Papke United States 12 583 0.8× 238 0.7× 81 0.5× 224 1.4× 30 0.2× 14 1.2k
Toshihito Fujii Japan 16 185 0.3× 262 0.8× 106 0.6× 114 0.7× 282 2.3× 54 913

Countries citing papers authored by Nicola Chiarelli

Since Specialization
Citations

This map shows the geographic impact of Nicola Chiarelli'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 Nicola Chiarelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicola Chiarelli more than expected).

Fields of papers citing papers by Nicola Chiarelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicola Chiarelli. 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 Nicola Chiarelli. The network helps show where Nicola Chiarelli may publish in the future.

Co-authorship network of co-authors of Nicola Chiarelli

This figure shows the co-authorship network connecting the top 25 collaborators of Nicola Chiarelli. A scholar is included among the top collaborators of Nicola Chiarelli 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 Nicola Chiarelli. Nicola Chiarelli 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.
Chiarelli, Nicola, Valeria Cinquina, Nicoletta Zoppi, et al.. (2024). Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts. Biomedicines. 12(12). 2749–2749. 1 indexed citations
2.
Ritelli, Marco, Nicola Chiarelli, Valeria Cinquina, et al.. (2023). Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers‐Danlos syndrome: A retrospective cross‐sectional study from an Italian reference center. American Journal of Medical Genetics Part A. 194(2). 174–194. 8 indexed citations
3.
Chiarelli, Nicola, Valeria Cinquina, Paolo Martini, et al.. (2023). Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(1). 166915–166915. 4 indexed citations
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Chiarelli, Nicola, Nicoletta Zoppi, Marco Ritelli, et al.. (2020). Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1867(4). 166051–166051. 17 indexed citations
6.
Ritelli, Marco, Eleonora Palagano, Valeria Cinquina, et al.. (2020). Genome-first approach for the characterization of a complex phenotype with combined NBAS and CUL4B deficiency. Bone. 140. 115571–115571. 7 indexed citations
7.
Ritelli, Marco, Valeria Cinquina, Edoardo Giacopuzzi, et al.. (2019). Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes. Genes. 10(9). 631–631. 25 indexed citations
8.
Zoppi, Nicoletta, et al.. (2018). Dermal fibroblast-to-myofibroblast transition sustained by αvß3 integrin-ILK-Snail1/Slug signaling is a common feature for hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(4). 1010–1023. 37 indexed citations
9.
Codenotti, Silvia, Marika Vezzoli, Pietro Luigi Poliani, et al.. (2016). Caveolin-1, Caveolin-2 and Cavin-1 are strong predictors of adipogenic differentiation in human tumors and cell lines of liposarcoma. European Journal of Cell Biology. 95(8). 252–264. 14 indexed citations
10.
Németh, Csilla, Paola Marcolongo, Alessandra Gamberucci, et al.. (2016). Glucose transporter type 10—lacking in arterial tortuosity syndrome—facilitates dehydroascorbic acid transport. FEBS Letters. 590(11). 1630–1640. 24 indexed citations
11.
Castori, Marco, Chiara Dordoni, Silvia Morlino, et al.. (2015). Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 43–53. 29 indexed citations
12.
Colombi, Marina, Chiara Dordoni, Nicola Chiarelli, & Marco Ritelli. (2015). Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers‐danlos syndrome hypermobility type compared to other heritable connective tissue disorders. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 6–22. 88 indexed citations
13.
Codenotti, Silvia, Pietro Luigi Poliani, Manuela Cominelli, et al.. (2015). MURC/cavin-4 Is Co-Expressed with Caveolin-3 in Rhabdomyosarcoma Tumors and Its Silencing Prevents Myogenic Differentiation in the Human Embryonal RD Cell Line. PLoS ONE. 10(6). e0130287–e0130287. 2 indexed citations
14.
Zoppi, Nicoletta, Nicola Chiarelli, Valeria Cinquina, Marco Ritelli, & Marina Colombi. (2015). GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts. Human Molecular Genetics. 24(23). 6769–6787. 40 indexed citations
15.
Chiarelli, Nicola, Marina Colombi, Stefania Mitola, et al.. (2015). Cavin-1 and Caveolin-1 are both required to support cell proliferation, migration and anchorage-independent cell growth in rhabdomyosarcoma. Laboratory Investigation. 95(6). 585–602. 33 indexed citations
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Dordoni, Chiara, Marco Ritelli, Marina Venturini, et al.. (2013). Recurring and Generalized Visceroptosis in Ehlers–Danlos Syndrome Hypermobility Type. American Journal of Medical Genetics Part A. 161(5). 1143–1147. 21 indexed citations
19.
Castori, Marco, Marco Ritelli, Nicoletta Zoppi, et al.. (2012). Adult presentation of arterial tortuosity syndrome in a 51‐year‐old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene. American Journal of Medical Genetics Part A. 158A(5). 1164–1169. 20 indexed citations
20.
Chiarelli, Nicola, Marco Ritelli, Nicoletta Zoppi, et al.. (2011). Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio. The International Journal of Developmental Biology. 55(2). 229–236. 8 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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