Giulia Melloni

658 total citations
10 papers, 167 citations indexed

About

Giulia Melloni is a scholar working on Neurology, Epidemiology and Genetics. According to data from OpenAlex, Giulia Melloni has authored 10 papers receiving a total of 167 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Neurology, 3 papers in Epidemiology and 3 papers in Genetics. Recurrent topics in Giulia Melloni's work include Neurofibromatosis and Schwannoma Cases (5 papers), Meningioma and schwannoma management (3 papers) and Craniofacial Disorders and Treatments (2 papers). Giulia Melloni is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (5 papers), Meningioma and schwannoma management (3 papers) and Craniofacial Disorders and Treatments (2 papers). Giulia Melloni collaborates with scholars based in Italy, Germany and United States. Giulia Melloni's co-authors include Federica Natacci, Roberto Ratiglia, Francesco Viola, Chiara Mapelli, Diego Vezzola, Angelo Selicorni, Edoardo Villani, Giulio Barteselli, Cesare Pirondini and Claudia Cesaretti and has published in prestigious journals such as Ophthalmology, Cancers and Cytogenetic and Genome Research.

In The Last Decade

Giulia Melloni

9 papers receiving 161 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giulia Melloni Italy 6 114 62 39 24 20 10 167
Cathérine Cassiman Belgium 11 101 0.9× 100 1.6× 127 3.3× 27 1.1× 49 2.5× 27 275
Brandon Worley United States 9 39 0.3× 45 0.7× 21 0.5× 14 0.6× 24 1.2× 25 198
Neil Shuey Australia 9 89 0.8× 28 0.5× 28 0.7× 22 0.9× 18 0.9× 22 198
Alessandra Protti Italy 8 145 1.3× 25 0.4× 47 1.2× 22 0.9× 21 1.1× 21 259
Elisa Vegezzi Italy 8 112 1.0× 25 0.4× 9 0.2× 9 0.4× 44 2.2× 26 209
Claudio Moratti Italy 6 63 0.6× 21 0.3× 14 0.4× 13 0.5× 14 0.7× 34 118
Shailee Shah United States 9 205 1.8× 22 0.4× 11 0.3× 37 1.5× 39 1.9× 30 297
Jun Sugasawa Japan 7 61 0.5× 59 1.0× 127 3.3× 27 1.1× 34 1.7× 42 232
Radek Frič Norway 11 99 0.9× 58 0.9× 11 0.3× 9 0.4× 29 1.4× 36 280
Guillaume Direz France 5 50 0.4× 36 0.6× 81 2.1× 131 5.5× 19 0.9× 7 253

Countries citing papers authored by Giulia Melloni

Since Specialization
Citations

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

Fields of papers citing papers by Giulia Melloni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Melloni

This figure shows the co-authorship network connecting the top 25 collaborators of Giulia Melloni. A scholar is included among the top collaborators of Giulia Melloni 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 Giulia Melloni. Giulia Melloni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
2.
Bianchessi, Donatella, Veronica Saletti, Rosina Paterra, et al.. (2020). Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients. Genes. 11(6). 671–671. 8 indexed citations
3.
Saletti, Veronica, Ilaria Viganò, Giulia Melloni, et al.. (2019). Chiari I malformation in defined genetic syndromes in children: are there common pathways?. Child s Nervous System. 35(10). 1727–1739. 12 indexed citations
4.
Melloni, Giulia, Marica Eoli, Claudia Cesaretti, et al.. (2019). Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort. Cancers. 11(12). 1838–1838. 17 indexed citations
5.
Tucci, Arianna, Veronica Saletti, Francesca Menni, et al.. (2017). The absence that makes the difference: choroidal abnormalities in Legius syndrome. Journal of Human Genetics. 62(11). 1001–1004. 5 indexed citations
6.
Natacci, Federica, Giulia Melloni, Francesca Motta, et al.. (2015). Delineating the Mosaic Trisomy 15 Phenotype Using a Serendipitous Mechanism as a Clue. Cytogenetic and Genome Research. 146(1). 44–50. 2 indexed citations
7.
Cesaretti, Claudia, Giulia Melloni, Roberto Fogliani, et al.. (2013). Neurofibromatosis type 1 and pregnancy: Maternal complications and attitudes about prenatal diagnosis. American Journal of Medical Genetics Part A. 161(2). 386–388. 16 indexed citations
8.
Gana, Simone, et al.. (2013). Prenatal phenotype of Nager syndrome and Rodriguez syndrome. Clinical Dysmorphology. 22(4). 135–139. 4 indexed citations
9.
Viola, Francesco, Edoardo Villani, Federica Natacci, et al.. (2011). Choroidal Abnormalities Detected by Near-Infrared Reflectance Imaging as a New Diagnostic Criterion for Neurofibromatosis 1. Ophthalmology. 119(2). 369–375. 95 indexed citations
10.
Cesaretti, Claudia, Barbara Gentilin, Vera Bianchi, et al.. (2011). Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations. Clinical Dysmorphology. 20(4). 229–231. 8 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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2026