Chiara Dordoni

1.2k citations
31 papers · 839 · h-index 16

Impact in

  • Genetics top 2%
    • Connective tissue disorders research
    • Dermatological and Skeletal Disorders
    • Neurogenetic and Muscular Disorders Research
  • Medical Terminology

Papers in

  • Genetics 27
    • Connective tissue disorders research 21
    • Dermatological and Skeletal Disorders 8
    • Genetic and Kidney Cyst Diseases 4
  • Molecular Biology 8
    • Ubiquitin and proteasome pathways 2
Co-authors
Marina Colombi (23 shared papers)Marco Ritelli (19 shared papers)Marina Venturini (18 shared papers)Nicola Chiarelli (10 shared papers)Piergiacomo Calzavara‐Pinton (12 shared papers)Marco Castori (9 shared papers)Paola Grammatico (6 shared papers)Silvia Morlino (7 shared papers)
Journals
Kidney International Reports (2 papers)Clinical Genetics (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (2 papers)European Journal of Medical Genetics (1 paper)Prenatal Diagnosis (1 paper)
Partner nations
ItalyLebanonUnited States

In The Last Decade

Chiara Dordoni

31 papers receiving 808 citations

Peers

Chiara Dordoni
Comparison fields: 5 of 58
  • Genetics 657
  • Medical Terminology 2
  • Rheumatology 118
  • Oncology 100
  • Immunology and Allergy 19
Replace Nicola Chiarelli with:
Nicola Chiarelli Italy
Christina M. Jacobsen United States
Irene Bottillo Italy
Sally Davies United Kingdom
Hariyadarshi Pannu United States
Martin P. Powers United States
Amina F. Zebboudj United States
Tracy L. Stewart United Kingdom
Toshihito Fujii Japan
Chalurmpon Srichomthong Thailand
Chiara Dordoni relative to Nicola Chiarelli Italy Nicola Chiarelli's profile →
Citations per field
00.5×1.5×2×
Nicola Chiarelli · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Chiara Dordoni, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Chiara Dordoni Line = papers co-authored together Chiara Dordoni links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Clinical and molecular characterization of 40 patients with classic Ehlers–Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations
Orphanet Journal of Rare Diseases ·Marco Ritelli, Chiara Dordoni, Marina Venturini, Nicola Chiarelli, Stefano Quinzani, Michele Traversa, Nicoletta Zoppi, Annalisa Vascellaro, Anita Wischmeijer, Emanuela Manfredini, Livia Garavelli, Piergiacomo Calzavara‐Pinton, Marina Colombi
201395
2
Small fiber neuropathy is a common feature of Ehlers-Danlos syndromes
Neurology ·Daniele Cazzato, Marco Castori, Raffaella Lombardi, Francesca Caravello, Eleonora Dalla Bella, Antonio Petrucci, Paola Grammatico, Chiara Dordoni, Marina Colombi, Giuseppe Lauria
201691
3
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 ·Marina Colombi, Chiara Dordoni, Nicola Chiarelli, Marco Ritelli
201588
4
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 ·Marco Castori, Silvia Morlino, Chiara Dordoni, Claudia Celletti, Filippo Camerota, Marco Ritelli, Aldo Morrone, Marina Venturini, Paola Grammatico, Marina Colombi
201273
5
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 ·Marco Castori, Chiara Dordoni, Michele Valiante, Isabella Sperduti, Marco Ritelli, Silvia Morlino, Nicola Chiarelli, Claudia Celletti, Marina Venturini, Filippo Camerota, Piergiacomo Calzavara‐Pinton, Paola Grammatico, Marina Colombi
201468
6
Transcriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type
PLoS ONE ·Nicola Chiarelli, Giulia Carini, Nicoletta Zoppi, Chiara Dordoni, Marco Ritelli, Marina Venturini, Marco Castori, Marina Colombi
201643
7
High prevalence of radiological vertebral fractures in adult patients with Ehlers–Danlos syndrome
Bone ·Gherardo Mazziotti, Chiara Dordoni, Mauro Doga, F. Galderisi, Marina Venturini, Piergiacomo Calzavara‐Pinton, Roberto Maroldi, (unknown), Marina Colombi
201542
8
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 ·Marina Colombi, Chiara Dordoni, Marina Venturini, Arianna Zanca, Piergiacomo Calzavara‐Pinton, Marco Ritelli
201633
9
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations
Molecular Genetics and Metabolism Reports ·Marco Ritelli, Nicola Chiarelli, Nicoletta Zoppi, Chiara Dordoni, Stefano Quinzani, Michele Traversa, Marina Venturini, Piergiacomo Calzavara‐Pinton, Marina Colombi
201430
10
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 ·Marco Castori, Chiara Dordoni, Silvia Morlino, Isabella Sperduti, Marco Ritelli, Michele Valiante, Nicola Chiarelli, Arianna Zanca, Claudia Celletti, Marina Venturini, Filippo Camerota, Piergiacomo Calzavara‐Pinton, Paola Grammatico, Marina Colombi
201529
11
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers‐Danlos syndrome patients
Clinical Genetics ·Marina Colombi, Chiara Dordoni, Marina Venturini, Claudia Ciaccio, Silvia Morlino, Nicola Chiarelli, Arianna Zanca, Piergiacomo Calzavara‐Pinton, Nicoletta Zoppi, Marco Castori, Marco Ritelli
201727
12
Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review
BMC Medical Genetics ·Marco Ritelli, Nicola Chiarelli, Chiara Dordoni, Elena Reffo, Marina Venturini, Stefano Quinzani, Matteo Della Monica, Gioacchino Scarano, Giuseppe Santoro, Maria Giovanna Russo, Piergiacomo Calzavara‐Pinton, Ornella Milanesi, Marina Colombi
201427
13
Further delineation of Loeys-Dietz syndrome type 4 in a family with mild vascular involvement and a TGFB2 splicing mutation
BMC Medical Genetics ·Marco Ritelli, Nicola Chiarelli, Chiara Dordoni, Stefano Quinzani, Marina Venturini, Roberto Maroldi, Piergiacomo Calzavara‐Pinton, Marina Colombi
201425
14
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney Disease
Kidney International Reports ·(unknown), Chiara Dordoni, Laura Econimo, Elisa Delbarba, Francesca Romana Grati, Eva Martin, Cinzia Mazza, Gianfranco Savoldi, Luca Rampoldi, Federico Alberici, Francesco Scolari
202023
15
Recurring and Generalized Visceroptosis in Ehlers–Danlos Syndrome Hypermobility Type
American Journal of Medical Genetics Part A ·Chiara Dordoni, Marco Ritelli, Marina Venturini, Nicola Chiarelli, Lidia Pezzani, Annalisa Vascellaro, Piergiacomo Calzavara‐Pinton, Marina Colombi
201322
16
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 ·Silvia Morlino, Chiara Dordoni, Isabella Sperduti, Marina Venturini, Claudia Celletti, Filippo Camerota, Marina Colombi, Marco Castori
201720
17
A classical Ehlers-Danlos syndrome family with incomplete presentation diagnosed by molecular testing
European Journal of Medical Genetics ·Marina Colombi, Chiara Dordoni, Valeria Cinquina, Marina Venturini, Marco Ritelli
201714
18
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 ·Chiara Dordoni, Claudia Ciaccio, Marina Venturini, Piergiacomo Calzavara‐Pinton, Marco Ritelli, Marina Colombi
201612
19
Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature review
American Journal of Medical Genetics Part A ·Chiara Dordoni, Claudia Ciaccio, Graziano Santoro, Marina Venturini, Ugo Cavallari, Marco Ritelli, Marina Colombi
201611
20
A novel MAP3K7 splice mutation causes cardiospondylocarpofacial syndrome with features of hereditary connective tissue disorder
European Journal of Human Genetics ·Silvia Morlino, Marco Castori, Chiara Dordoni, Valeria Cinquina, Graziano Santoro, Paola Grammatico, Marina Venturini, Marina Colombi, Marco Ritelli
201811

About Chiara Dordoni

Chiara Dordoni is a scholar working on Genetics, Molecular Biology, Oncology, Surgery and Pediatrics, Perinatology and Child Health, having authored 31 papers that have together received 839 indexed citations. Recurring topics across this work include Connective tissue disorders research (21 papers), Dermatological and Skeletal Disorders (8 papers), Bone health and treatments (5 papers), Genetic and Kidney Cyst Diseases (4 papers), Dupuytren's Contracture and Treatments (3 papers), Ubiquitin and proteasome pathways (2 papers), Pregnancy-related medical research (2 papers) and Protease and Inhibitor Mechanisms (2 papers). The work is most often cited by research in Genetics (657 citations), Medical Terminology (2 citations), Rheumatology (118 citations), Oncology (100 citations) and Immunology and Allergy (19 citations). Chiara Dordoni has collaborated with scholars based in Italy, Lebanon and United States. Frequent co-authors include Marina Colombi, Marco Ritelli, Marina Venturini, Nicola Chiarelli, Piergiacomo Calzavara‐Pinton, Marco Castori, Paola Grammatico, Silvia Morlino, Nicoletta Zoppi and Filippo Camerota. Their work appears in journals such as Kidney International Reports, Clinical Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, European Journal of Medical Genetics and Prenatal Diagnosis.

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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