Chiara Dordoni

1.2k total citations
31 papers, 820 citations indexed

About

Chiara Dordoni is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Chiara Dordoni has authored 31 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Oncology. Recurrent topics in Chiara Dordoni's work include Connective tissue disorders research (22 papers), Dermatological and Skeletal Disorders (9 papers) and Bone health and treatments (5 papers). Chiara Dordoni is often cited by papers focused on Connective tissue disorders research (22 papers), Dermatological and Skeletal Disorders (9 papers) and Bone health and treatments (5 papers). Chiara Dordoni collaborates with scholars based in Italy, Lebanon and United States. Chiara Dordoni's co-authors include Marina Colombi, Marco Ritelli, Marina Venturini, Nicola Chiarelli, Piergiacomo Calzavara‐Pinton, Marco Castori, Paola Grammatico, Silvia Morlino, Nicoletta Zoppi and Claudia Celletti and has published in prestigious journals such as PLoS ONE, Neurology and American Journal of Kidney Diseases.

In The Last Decade

Chiara Dordoni

31 papers receiving 789 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chiara Dordoni Italy 16 668 219 153 141 121 31 820
Nicola Chiarelli Italy 22 724 1.1× 340 1.6× 178 1.2× 158 1.1× 124 1.0× 40 1.0k
Francesca Crosti Italy 14 195 0.3× 278 1.3× 90 0.6× 96 0.7× 73 0.6× 40 884
Caroline Michot France 16 436 0.7× 395 1.8× 144 0.9× 89 0.6× 109 0.9× 43 823
Toshihito Fujii Japan 16 185 0.3× 262 1.2× 106 0.7× 114 0.8× 282 2.3× 54 913
Chalurmpon Srichomthong Thailand 16 356 0.5× 342 1.6× 116 0.8× 74 0.5× 29 0.2× 49 676
Yumiko Okubo Japan 10 135 0.2× 336 1.5× 83 0.5× 77 0.5× 82 0.7× 27 791
N C Nevin United Kingdom 18 332 0.5× 324 1.5× 40 0.3× 198 1.4× 36 0.3× 32 851
Belinda Chong Australia 15 169 0.3× 271 1.2× 47 0.3× 69 0.5× 126 1.0× 27 617
Amina F. Zebboudj United States 7 164 0.2× 270 1.2× 169 1.1× 81 0.6× 58 0.5× 7 753
Monika Grabowski Germany 6 722 1.1× 490 2.2× 336 2.2× 90 0.6× 344 2.8× 7 1.7k

Countries citing papers authored by Chiara Dordoni

Since Specialization
Citations

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

Fields of papers citing papers by Chiara Dordoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Dordoni

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Dordoni. A scholar is included among the top collaborators of Chiara Dordoni 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 Chiara Dordoni. Chiara Dordoni 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.
Dordoni, Chiara, Letizia Zeni, Cinzia Mazza, et al.. (2024). Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease–spectrum phenotype. Clinical Kidney Journal. 17(2). sfae026–sfae026. 5 indexed citations
2.
Zeni, Letizia, Federica Mescia, Chiara Dordoni, et al.. (2024). Clinical Significance of the Cystic Phenotype in Alport Syndrome. American Journal of Kidney Diseases. 84(3). 320–328.e1. 5 indexed citations
3.
Bedeschi, Maria Francesca, Claudia Izzi, Chiara Dordoni, et al.. (2023). Identification of bi‐allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3. Clinical Genetics. 104(2). 230–237. 1 indexed citations
4.
Delbarba, Elisa, Laura Econimo, Chiara Dordoni, et al.. (2021). Expanding the variability of the ADPKD-GANAB clinical phenotype in a family of Italian ancestry. Journal of Nephrology. 35(2). 645–652. 6 indexed citations
5.
Izzi, Claudia, Chiara Dordoni, Laura Econimo, et al.. (2020). Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney Disease. Kidney International Reports. 5(12). 2341–2350. 22 indexed citations
6.
Dordoni, Chiara, Federico Prefumo, Maria Iascone, et al.. (2019). Prenatal findings in oral‐facial‐digital syndrome type VI: Report of three cases and literature review. Prenatal Diagnosis. 39(8). 652–655. 2 indexed citations
7.
Morlino, Silvia, Marco Castori, Chiara Dordoni, et al.. (2018). A novel MAP3K7 splice mutation causes cardiospondylocarpofacial syndrome with features of hereditary connective tissue disorder. European Journal of Human Genetics. 26(4). 582–586. 11 indexed citations
8.
Colombi, Marina, Chiara Dordoni, Valeria Cinquina, Marina Venturini, & Marco Ritelli. (2017). A classical Ehlers-Danlos syndrome family with incomplete presentation diagnosed by molecular testing. European Journal of Medical Genetics. 61(1). 17–20. 14 indexed citations
9.
Dordoni, Chiara, Marta Gatti, Marina Venturini, et al.. (2017). Characterization of a Pseudoxanthoma elasticum-like patient with coagulation deficiency, cutaneous calcinosis and GGCX compound heterozygosity. Journal of Dermatological Science. 89(2). 201–204. 2 indexed citations
10.
Morlino, Silvia, Chiara Dordoni, Isabella Sperduti, et al.. (2017). Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers–Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part A. 173(4). 914–929. 19 indexed citations
11.
Colombi, Marina, Chiara Dordoni, Marina Venturini, et al.. (2016). Delineation of Ehlers–Danlos syndrome phenotype due to the c.934C>T, p.(Arg312Cys) mutation in COL1A1: Report on a three‐generation family without cardiovascular events, and literature review. American Journal of Medical Genetics Part A. 173(2). 524–530. 33 indexed citations
12.
Dordoni, Chiara, Claudia Ciaccio, Marina Venturini, et al.. (2016). Further delineation of FKBP14‐related Ehlers–Danlos syndrome: A patient with early vascular complications and non‐progressive kyphoscoliosis, and literature review. American Journal of Medical Genetics Part A. 170(8). 2031–2038. 12 indexed citations
13.
Ciaccio, Claudia, Chiara Dordoni, Marco Ritelli, & Marina Colombi. (2016). Koolen-de Vries Syndrome: Clinical Report of an Adult and Literature Review. Cytogenetic and Genome Research. 150(1). 40–45. 9 indexed citations
14.
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
15.
16.
Ritelli, Marco, Nicola Chiarelli, Chiara Dordoni, et al.. (2014). Further delineation of Loeys-Dietz syndrome type 4 in a family with mild vascular involvement and a TGFB2 splicing mutation. BMC Medical Genetics. 15(1). 91–91. 23 indexed citations
17.
18.
Castori, Marco, Chiara Dordoni, Isabella Sperduti, et al.. (2014). Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees. American Journal of Medical Genetics Part A. 164(12). 3010–3020. 68 indexed citations
19.
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
20.
Castori, Marco, Silvia Morlino, Chiara Dordoni, et al.. (2012). Gynecologic and obstetric implications of the joint hypermobility syndrome (a.k.a. Ehlers–Danlos syndrome hypermobility type) in 82 Italian patients. American Journal of Medical Genetics Part A. 158A(9). 2176–2182. 73 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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