Maria Gnoli

483 total citations
28 papers, 209 citations indexed

About

Maria Gnoli is a scholar working on Rheumatology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Maria Gnoli has authored 28 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Rheumatology, 16 papers in Genetics and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Maria Gnoli's work include Connective tissue disorders research (10 papers), Bone Tumor Diagnosis and Treatments (9 papers) and Sarcoma Diagnosis and Treatment (6 papers). Maria Gnoli is often cited by papers focused on Connective tissue disorders research (10 papers), Bone Tumor Diagnosis and Treatments (9 papers) and Sarcoma Diagnosis and Treatment (6 papers). Maria Gnoli collaborates with scholars based in Italy, Switzerland and Germany. Maria Gnoli's co-authors include Luca Sangiorgi, Elena Pedrini, Morena Tremosini, Marina Mordenti, Mauro Celli, P D’Eufemia, Paolo Versacci, Anita Wischmeijer, Evelise Brizola and Cecilia Giunta and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Bone.

In The Last Decade

Maria Gnoli

25 papers receiving 205 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Gnoli Italy 8 126 103 50 49 24 28 209
Zayed Al‐Zayed Saudi Arabia 7 155 1.2× 82 0.8× 13 0.3× 63 1.3× 40 1.7× 17 259
Ewelina Bukowska‐Olech Poland 11 147 1.2× 33 0.3× 18 0.4× 157 3.2× 11 0.5× 41 273
Azmy M. Al-Hadidy Jordan 9 89 0.7× 24 0.2× 44 0.9× 94 1.9× 11 0.5× 21 274
Margo Whiteford United Kingdom 11 193 1.5× 58 0.6× 43 0.9× 194 4.0× 10 0.4× 15 398
Johanna Dahlqvist Sweden 11 78 0.6× 59 0.6× 78 1.6× 150 3.1× 21 0.9× 17 347
Fulan Wei China 9 60 0.5× 22 0.2× 35 0.7× 130 2.7× 26 1.1× 23 313
Randi Koll Germany 9 152 1.2× 31 0.3× 26 0.5× 206 4.2× 44 1.8× 13 346
N Kremenevskaja Germany 5 56 0.4× 27 0.3× 38 0.8× 263 5.4× 19 0.8× 7 410
Magdalena Socha Poland 10 113 0.9× 26 0.3× 39 0.8× 143 2.9× 9 0.4× 24 260
Marilena Carmela Di Giacomo Italy 9 140 1.1× 18 0.2× 39 0.8× 148 3.0× 12 0.5× 14 278

Countries citing papers authored by Maria Gnoli

Since Specialization
Citations

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

Fields of papers citing papers by Maria Gnoli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Gnoli

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Gnoli. A scholar is included among the top collaborators of Maria Gnoli 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 Maria Gnoli. Maria Gnoli 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.
Pedrini, Elena, Morena Tremosini, Dario Cocciadiferro, et al.. (2025). Further Evidence of Early-Onset Osteoporosis and Bone Fractures as a New FGFR2-Related Phenotype. International Journal of Molecular Sciences. 26(9). 4204–4204.
2.
Morri, Mattia, Morena Tremosini, Cristiana Forni, et al.. (2025). Pain intensity in patients with genetic metabolic bone diseases: an observational study. Bone. 203. 117736–117736. 1 indexed citations
3.
Bartolotti, Isabella, et al.. (2024). A Novel Pathogenic Large Duplication in EXT1 Identified in a Family with Multiple Osteochondromas. Genes. 15(9). 1169–1169.
4.
5.
Gnoli, Maria, Marco Gambarotti, Alberto Righi, et al.. (2024). Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series. Orphanet Journal of Rare Diseases. 19(1). 63–63. 2 indexed citations
6.
Mordenti, Marina, Federico Banchelli, Diego Antonioli, et al.. (2024). Osteogenesis imperfecta: a cross-sectional study of skeletal and extraskeletal features in a large cohort of Italian patients. Frontiers in Endocrinology. 14. 1299232–1299232. 1 indexed citations
7.
Brizola, Evelise, et al.. (2023). Pathological mandibular fracture complicated by osteonecrosis in an adult patient with pycnodysostosis: clinical report and review of the literature. European Journal of Medical Genetics. 67. 104904–104904. 2 indexed citations
8.
Gnoli, Maria, et al.. (2023). Vitamin D and Bone fragility in Individuals with Osteogenesis Imperfecta: A Scoping Review. International Journal of Molecular Sciences. 24(11). 9416–9416. 5 indexed citations
9.
Mordenti, Marina, Morena Tremosini, Manuela Locatelli, et al.. (2023). Cost-effectiveness of bringing a nurse into an Italian genetic day clinic: a before and after study. BMC Health Services Research. 23(1). 1278–1278. 2 indexed citations
10.
Pedrini, Elena, V.L. Pecoraro, Maria Gnoli, et al.. (2022). Real-World Data and Budget Impact Analysis (BIA): Evaluation of a Targeted Next-Generation Sequencing Diagnostic Approach in Two Orthopedic Rare Diseases. Frontiers in Pharmacology. 13. 785705–785705. 1 indexed citations
11.
Righi, Alberto, Marina Pacheco, Stefania Cocchi, et al.. (2022). Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survival. Orphanet Journal of Rare Diseases. 17(1). 74–74. 6 indexed citations
12.
Gnoli, Maria, Evelise Brizola, Morena Tremosini, et al.. (2021). COL1-Related Disorders: Case Report and Review of Overlapping Syndromes. Frontiers in Genetics. 12. 640558–640558. 13 indexed citations
13.
Brizola, Evelise, Maria Gnoli, Morena Tremosini, et al.. (2020). Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation. Molecular Genetics & Genomic Medicine. 8(9). e1353–e1353. 5 indexed citations
14.
Mordenti, Marina, Fei F. Shih, Elena Pedrini, et al.. (2020). The natural history of multiple osteochondromas in a large Italian cohort of pediatric patients. Bone. 139. 115499–115499. 11 indexed citations
15.
Gnoli, Maria, Eric L. Staals, L Campanacci, et al.. (2019). Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series. Calcified Tissue International. 105(2). 215–221. 6 indexed citations
16.
Lindert, Uschi, Maria Gnoli, Maria Francesca Bedeschi, et al.. (2017). Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta. Calcified Tissue International. 102(3). 373–379. 12 indexed citations
17.
18.
Bozzola, Mauro, Maria Gnoli, Federico Baronio, et al.. (2015). Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 53–53. 6 indexed citations
19.
Wischmeijer, Anita, Pamela Magini, Roberto Giorda, et al.. (2010). Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype. Molecular Syndromology. 1(4). 176–184. 23 indexed citations
20.
Drera, Bruno, Marco Ritelli, Nicoletta Zoppi, et al.. (2009). Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients. Orphanet Journal of Rare Diseases. 4(1). 24–24. 18 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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