Giulia Melloni

673 citations
11 papers · 520 · h-index 7

Impact in

  • Neurology top 10%
    • Neurofibromatosis and Schwannoma Cases
    • Vascular Malformations Diagnosis and Treatment
    • BRCA gene mutations in cancer
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities

Papers in

    • Neurofibromatosis and Schwannoma Cases 5
    • Genomic variations and chromosomal abnormalities 2
    • Craniofacial Disorders and Treatments 2
    • Congenital Ear and Nasal Anomalies 1
    • Genetic Syndromes and Imprinting 1

Giulia Melloni

10 papers receiving 506 citations

Peers

Giulia Melloni
Comparison fields: 5 of 75
  • Neurology 132
  • Genetics 178
  • Reproductive Medicine 37
  • Cancer Research 60
  • Ophthalmology 27
Replace Kuang Lin Ying with:
Kuang Lin Ying United States
N Kanda Japan
Kusum P. Lele United States
A. M. Vagner‐Capodano France
Salah A. D. Ebrahim United States
Katharina Mößinger Germany
Barbara Grammatico Italy
Aleksander Jamsheer Poland
Silvia Genovese Italy
Baoheng Gui China
Giulia Melloni relative to Kuang Lin Ying United States Kuang Lin Ying's profile →
Citations per field
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Citations per year

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-authors

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

All Works

11 of 11 papers shown
#Work
1 2013328
2 2011107
3 201920
4 201319
5 201914
6 20209
7 20118
8 20177
9 20135
10 20153
11 20240

About Giulia Melloni

Giulia Melloni is a scholar working on Neurology, Genetics, Ophthalmology, Pulmonary and Respiratory Medicine and Genetics, having authored 11 papers that have together received 520 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (5 papers), Meningioma and schwannoma management (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Craniofacial Disorders and Treatments (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Congenital Ear and Nasal Anomalies (1 paper), Tracheal and airway disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Neurology (132 citations), Genetics (178 citations), Reproductive Medicine (37 citations), Cancer Research (60 citations) and Ophthalmology (27 citations). Giulia Melloni has collaborated with scholars based in Italy, Germany and United Kingdom. Frequent co-authors include Federica Natacci, Francesco Viola, Angelo Selicorni, Chiara Mapelli, Edoardo Villani, Roberto Ratiglia, Diego Vezzola, Giulio Barteselli, Cesare Pirondini and Veronica Saletti. Their work appears in journals such as Genes, Ophthalmology, Cancers, Cytogenetic and Genome Research and Child s Nervous System.

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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