Marco Ritelli

2.8k citations
79 papers · 1.6k · h-index 25

Impact in

  • Genetics top 2%
    • Connective tissue disorders research
    • Dermatological and Skeletal Disorders
  • Rheumatology top 5%
    • Dupuytren's Contracture and Treatments

Papers in

  • Genetics 65
    • Connective tissue disorders research 61
    • Dermatological and Skeletal Disorders 30
  • Molecular Biology 30
    • Wnt/β-catenin signaling in development and cancer 7
    • Ubiquitin and proteasome pathways 6
Co-authors
Marina Colombi (71 shared papers)Nicola Chiarelli (37 shared papers)Nicoletta Zoppi (27 shared papers)Marina Venturini (31 shared papers)Chiara Dordoni (19 shared papers)Valeria Cinquina (21 shared papers)Piergiacomo Calzavara‐Pinton (12 shared papers)Marco Castori (14 shared papers)
Journals
Genes (6 papers)Orphanet Journal of Rare Diseases (4 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (4 papers)European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)
Partner nations
ItalyUnited StatesBelgium

In The Last Decade

Marco Ritelli

78 papers receiving 1.5k citations

Peers

Marco Ritelli
Comparison fields: 5 of 100
  • Genetics 1.1k
  • Rheumatology 269
  • Medical Terminology 2
  • Nephrology 56
  • Neurology 110
Replace Nicola Chiarelli with:
Nicola Chiarelli Italy
Matthew J. Simmonds United Kingdom
Michael B. Bober United States
Renata Bocciardi Italy
Olivier Vanakker Belgium
Jelena Martinović France
J. M. Heward United Kingdom
Nazli B. McDonnell United States
Emily L. Germain‐Lee United States
Takahiro Tsujimura Japan
Marco Ritelli relative to Nicola Chiarelli Italy Nicola Chiarelli's profile →
Citations per field
00.5×1.5×2×2.3×
Nicola Chiarelli · 1×
Citations per year

Countries citing papers authored by Marco Ritelli

Since Specialization
Citations

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

Fields of papers citing papers by Marco Ritelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Marco Ritelli, 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 Marco Ritelli Line = papers co-authored together Marco Ritelli links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 79 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
201393
2
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
3
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
4
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
5
Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes
Genes ·Nicola Chiarelli, Marco Ritelli, Nicoletta Zoppi, Marina Colombi
201948
6
Thoracic Aortic Aneurysm in Infancy in Aneurysms–Osteoarthritis Syndrome Due to a Novel SMAD3 Mutation: Further Delineation of the Phenotype
American Journal of Medical Genetics Part A ·Anita Wischmeijer, Lut Van Laer, Giada Tortora, Nikhita Bolar, Guy Van Camp, Erik Fransén, Nils Peeters, Roberto Di Bartolomeo, Davide Pacini, Gaetano Gargiulo, Simone Turci, Marco Bonvicini, Elisabetta Mariucci, Luigi Lovato, S Brusori, Marco Ritelli, Marina Colombi, Livia Garavelli, Marco Seri, Bart Loeys
201347
7
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
201641
8
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 ·Nicoletta Zoppi, Nicola Chiarelli, Valeria Cinquina, Marco Ritelli, Marina Colombi
201540
9
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 ·Nicoletta Zoppi, Nicola Chiarelli, Silvia Binetti, Marco Ritelli, Marina Colombi
201837
10
Connective tissue anomalies in patients with spontaneous cervical artery dissection
Neurology ·Alessia Giossi, Marco Ritelli, Paolo Costa, Andrea Morotti, Loris Poli, Elisabetta Del Zotto, Irene Volonghi, Nicola Chiarelli, Massimo Gamba, Paolo Bovi, Giampaolo Tomelleri, Monica Carletti, Nicoletta Checcarelli, Giorgio Meneghetti, M Morra, Mauro Chinaglia, Valeria De Giuli, Marina Colombi, Alessandro Padovani, Alessandro Pezzini
201436
11
Complications of Acute Stroke and the Occurrence of Early Seizures
Cerebrovascular Diseases ·Alessandro Pezzini, Mario Grassi, Elisabetta Del Zotto, Alessia Giossi, Irene Volonghi, Paolo Costa, Loris Poli, Andrea Morotti, Massimo Gamba, Marco Ritelli, Marina Colombi, Alessandro Padovani
201335
12
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome
PLoS ONE ·Nicola Chiarelli, Giulia Carini, Nicoletta Zoppi, Marco Ritelli, Marina Colombi
201834
13
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
14
Arterial tortuosity in patients with spontaneous cervical artery dissection
Neuroradiology ·Alessia Giossi, Dikran Mardighian, Filomena Caria, Loris Poli, Valeria De Giuli, Paolo Costa, Andrea Morotti, Massimo Gamba, Nicola Gilberti, Marco Ritelli, Marina Colombi, Maria Sessa, Mario Grassi, Alessandro Padovani, Roberto Gasparotti, Alessandro Pezzini
201731
15
A Novel Homozygous <b><i>SLC2A9</i></b> Mutation Associated with Renal-Induced Hypouricemia
American Journal of Nephrology ·Martin Windpessl, Marco Ritelli, Manfred Wallner, Marina Colombi
201630
16
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
17
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
18
Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives
Orphanet Journal of Rare Diseases ·Marco Ritelli, Marina Venturini, Valeria Cinquina, Nicola Chiarelli, Marina Colombi
202028
19
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients’ skin fibroblasts
PLoS ONE ·Nicola Chiarelli, Giulia Carini, Nicoletta Zoppi, Marco Ritelli, Marina Colombi
201928
20
Spontaneous coronary artery dissection in a young woman with Loeys–Dietz syndrome
American Journal of Medical Genetics Part A ·Rossella Fattori, Pietro Sangiorgio, Elisabetta Mariucci, Marco Ritelli, Anita Wischmeijer, Cristiano Greco, Marina Colombi
201228

About Marco Ritelli

Marco Ritelli is a scholar working on Genetics, Molecular Biology, Rheumatology, Oncology and Cell Biology, having authored 79 papers that have together received 1.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (61 papers), Dermatological and Skeletal Disorders (30 papers), Wnt/β-catenin signaling in development and cancer (7 papers), Dupuytren's Contracture and Treatments (7 papers), Cardiovascular Issues in Pregnancy (7 papers), Bone health and treatments (6 papers), Ubiquitin and proteasome pathways (6 papers) and Cell Adhesion Molecules Research (5 papers). The work is most often cited by research in Genetics (1.1k citations), Rheumatology (269 citations), Medical Terminology (2 citations), Nephrology (56 citations) and Neurology (110 citations). Marco Ritelli has collaborated with scholars based in Italy, United States and Belgium. Frequent co-authors include Marina Colombi, Nicola Chiarelli, Nicoletta Zoppi, Marina Venturini, Chiara Dordoni, Valeria Cinquina, Piergiacomo Calzavara‐Pinton, Marco Castori, Paola Grammatico and Silvia Morlino. Their work appears in journals such as Genes, Orphanet Journal of Rare Diseases, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, European Journal of Human Genetics and Clinical Genetics.

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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