Marco Ritelli

2.9k citations
101 papers · 2.2k · h-index 29

Impact in

  • Genetics top 2%
    • Connective tissue disorders research
    • Genomics and Rare Diseases
  • Neurology top 10%
    • Intracerebral and Subarachnoid Hemorrhage Research

Papers in

  • Genetics 78
    • Connective tissue disorders research 70
    • Genomics and Rare Diseases 7
    • Dermatological and Skeletal Disorders 5
  • Neurology 8
    • Intracerebral and Subarachnoid Hemorrhage Research 7
Co-authors
Marina Colombi (80 shared papers)Nicola Chiarelli (39 shared papers)Nicoletta Zoppi (29 shared papers)Marina Venturini (38 shared papers)Chiara Dordoni (23 shared papers)Valeria Cinquina (23 shared papers)Piergiacomo Calzavara‐Pinton (18 shared papers)Marco Castori (14 shared papers)
Journals
Genes (7 papers)Journal of Dermatological Science (5 papers)Orphanet Journal of Rare Diseases (5 papers)Clinical Genetics (4 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (4 papers)
Partner nations
ItalySwitzerlandBelgium

In The Last Decade

Marco Ritelli

97 papers receiving 2.1k citations

Peers

Marco Ritelli
Comparison fields: 5 of 92
  • Genetics 1.3k
  • Neurology 157
  • Developmental Biology 17
  • Cell Biology 87
  • Nephrology 51
Replace Mine Arslan‐Kirchner with:
Mine Arslan‐Kirchner Germany
V. V. Smith United Kingdom
Mari Wataya‐Kaneda Japan
Anne M. De Paepe Belgium
Atsuo Kikuchi Japan
Mara Giordano Italy
Irina Giurgea France
Hiromichi Hamada Japan
Emilio Arteaga‐Solis United States
Ramakrishnan Rajagopalan United States
Marco Ritelli relative to Mine Arslan‐Kirchner Germany Mine Arslan‐Kirchner's profile →
Citations per field
00.5×2×4×5.1×
Mine Arslan‐Kirchner · 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 101 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
2013106
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
2015101
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
201280
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
201470
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
201960
6
Thoracic Aortic Aneurysm in Infancy in Aneurysms– O steoarthritis Syndrome Due to a Novel SMAD 3 Mutation: Further Delineation of the Phenotype
American Journal of Medical Genetics Part A ·Anita Wischmeijer, Lut Van Laer, Giada Tortora, Nikhita Ajit Bolar, Guy Van Camp, Erik Fransén, Nils Peeters, Roberto Di Bartolomeo
201354
7
Obesity and the Risk of Intracerebral Hemorrhage
Stroke ·Alessandro Pezzini, Mario Grassi, Maurizio Paciaroni, Andrea Zini, Giorgio Silvestrelli, Licia Iacoviello, Augusto Filippo Di Castelnuovo, Elisabetta Del Zotto
201350
8
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
201647
9
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β
Science Immunology ·Juan Li, Marco Ritelli, Cindy S. Ma, Geetha Rao, Tanwir Habib, Emilie Corvilain, Salim Bougarn, Sophie Cypowyj
201946
10
Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders
Genes ·Marco Ritelli, Marina Colombi
202046
11
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
201544
12
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
201343
13
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
201843
14
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
201440
15
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
201838
16
COL1 ‐related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers‐Danlos syndrome overlap
Clinical Genetics ·Silvia Morlino, Lucia Micale, Marco Ritelli, Marianne Rohrbach, Nicoletta Zoppi, Anthony Vandersteen, Sara B. MacKay, Emanuele Agolini
201938
17
Serum cholesterol levels, HMG-CoA reductase inhibitors and the risk of intracerebral haemorrhage. The Multicenter Study on Cerebral Haemorrhage in Italy (MUCH-Italy)
Journal of Neurology Neurosurgery & Psychiatry ·Alessandro Pezzini, Mario Grassi, Licia Iacoviello, Marialuisa Zedde, Simona Marcheselli, Giorgio Silvestrelli, Maria Luisa DeLodovici, Maria Sessa
201637
18
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
201635
19
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
202034
20
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
201433

About Marco Ritelli

Marco Ritelli is a scholar working on Genetics, Neurology, Cell Biology, Immunology and Allergy and Pulmonary and Respiratory Medicine, having authored 101 papers that have together received 2.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (70 papers), Genomics and Rare Diseases (7 papers), Intracerebral and Subarachnoid Hemorrhage Research (7 papers), Dermatological and Skeletal Disorders (5 papers), Skin and Cellular Biology Research (3 papers), Cerebrovascular and Carotid Artery Diseases (3 papers), Tuberculosis Research and Epidemiology (2 papers) and TGF-β signaling in diseases (2 papers). The work is most often cited by research in Genetics (1.3k citations), Neurology (157 citations), Developmental Biology (17 citations), Cell Biology (87 citations) and Nephrology (51 citations). Marco Ritelli has collaborated with scholars based in Italy, Switzerland 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, Journal of Dermatological Science, Orphanet Journal of Rare Diseases, Clinical Genetics and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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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