Simona Mellone

572 total citations
31 papers, 373 citations indexed

About

Simona Mellone is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Simona Mellone has authored 31 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 11 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Simona Mellone's work include Growth Hormone and Insulin-like Growth Factors (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Syndromes and Imprinting (5 papers). Simona Mellone is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Syndromes and Imprinting (5 papers). Simona Mellone collaborates with scholars based in Italy, United States and Russia. Simona Mellone's co-authors include Mara Giordano, Michela Godi, Flavia Prodam, Gianni Bona, Simonetta Bellone, Antonella Petri, Sandra D’Alfonso, Lucia Corrado, Patricia Momigliano‐Richiardi and Yari Carlomagno and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and Neurobiology of Aging.

In The Last Decade

Simona Mellone

29 papers receiving 370 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simona Mellone Italy 13 158 147 133 54 46 31 373
P Bouloux United Kingdom 6 68 0.4× 146 1.0× 159 1.2× 87 1.6× 21 0.5× 7 466
Gabriela Carreno United Kingdom 12 172 1.1× 49 0.3× 219 1.6× 32 0.6× 88 1.9× 18 415
Mark J. McCabe United Kingdom 16 234 1.5× 259 1.8× 331 2.5× 37 0.7× 73 1.6× 22 707
Alicia S. Martínez Argentina 10 377 2.4× 256 1.7× 238 1.8× 43 0.8× 27 0.6× 16 582
Louise Gregory United Kingdom 14 258 1.6× 171 1.2× 224 1.7× 31 0.6× 58 1.3× 25 520
Jean-François Vanbellinghen Belgium 10 110 0.7× 74 0.5× 149 1.1× 65 1.2× 154 3.3× 18 542
Elisabetta Pelo Italy 11 88 0.6× 80 0.5× 216 1.6× 11 0.2× 52 1.1× 36 480
Youn Hee Jee United States 13 147 0.9× 173 1.2× 253 1.9× 13 0.2× 14 0.3× 30 506
Kyriaki S. Alatzoglou United Kingdom 15 491 3.1× 327 2.2× 334 2.5× 37 0.7× 68 1.5× 23 821
Hiroki Ueharu Japan 13 144 0.9× 69 0.5× 264 2.0× 26 0.5× 42 0.9× 33 437

Countries citing papers authored by Simona Mellone

Since Specialization
Citations

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

Fields of papers citing papers by Simona Mellone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simona Mellone

This figure shows the co-authorship network connecting the top 25 collaborators of Simona Mellone. A scholar is included among the top collaborators of Simona Mellone 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 Simona Mellone. Simona Mellone 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.
2.
Costa, Federica, Simona Mellone, Elena Boggio, et al.. (2023). Genes and Microbiota Interaction in Monogenic Autoimmune Disorders. Biomedicines. 11(4). 1127–1127. 2 indexed citations
3.
Daffara, Tommaso, Giovanni Ceccarini, Caterina Pelosini, et al.. (2023). A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature. Frontiers in Endocrinology. 14. 1212729–1212729. 7 indexed citations
4.
Savastio, Silvia, et al.. (2023). Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variants. Frontiers in Endocrinology. 14. 1143736–1143736. 3 indexed citations
5.
Mellone, Simona, Chiara Puricelli, Cinzia Peruzzi, et al.. (2022). The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders. Frontiers in Genetics. 13. 875182–875182. 12 indexed citations
6.
Prodam, Flavia, Simona Mellone, Roberta Ricotti, et al.. (2021). Retrospective Diagnosis of a Novel ACAN Pathogenic Variant in a Family With Short Stature: A Case Report and Review of the Literature. Frontiers in Genetics. 12. 708864–708864. 7 indexed citations
7.
Cugno, Massimo, Paolo Macor, Mara Giordano, et al.. (2021). Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination. Journal of Autoimmunity. 124. 102728–102728. 4 indexed citations
8.
Rolla, Roberta, Chiara Puricelli, Simona Mellone, et al.. (2020). Screening for haemoglobin disorders: The experience of the piedmont north‐eastern quadrant. International Journal of Laboratory Hematology. 43(2). 1 indexed citations
9.
Vannelli, Silvia, Simona Mellone, Lucia Corrado, et al.. (2020). Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency. European Journal of Human Genetics. 29(1). 110–121. 12 indexed citations
10.
Monzani, Alice, Simona Mellone, Giulia Genoni, et al.. (2019). Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies. BMC Medical Genomics. 12(1). 5–5. 8 indexed citations
11.
Musetti, Claudio, Simona Mellone, Marco Quaglia, et al.. (2016). Testing for the cytosine insertion in the VNTR of the MUC1 gene in a cohort of Italian patients with autosomal dominant tubulointerstitial kidney disease. Journal of Nephrology. 29(3). 451–455. 8 indexed citations
12.
Rienzo, Francesca De, Simona Mellone, Simonetta Bellone, et al.. (2015). Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort. Clinical Endocrinology. 83(6). 849–860. 60 indexed citations
13.
Mellone, Simona, Nadia Barizzone, Flavia Prodam, et al.. (2015). Variations in the high-mobility group-A2 gene (HMGA2) are associated with idiopathic short stature. Pediatric Research. 79(2). 258–261. 5 indexed citations
14.
Barizzone, Nadia, Sara Monti, Simona Mellone, et al.. (2013). Rare Variants in theTREX1Gene and Susceptibility to Autoimmune Diseases. BioMed Research International. 2013. 1–6. 27 indexed citations
15.
Vivenza, Daniela, Michela Godi, Maria Felicia Faienza, et al.. (2011). A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing. European Journal of Endocrinology. 164(5). 705–713. 11 indexed citations
16.
Barizzone, Nadia, Maurizio Marchini, Annalisa Chiocchetti, et al.. (2011). Association of osteopontin regulatory polymorphisms with systemic sclerosis. Human Immunology. 72(10). 930–934. 32 indexed citations
17.
Corrado, Lucia, Yari Carlomagno, Simona Mellone, et al.. (2010). A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient. Neurobiology of Aging. 32(3). 552.e1–552.e6. 46 indexed citations
18.
Carlomagno, Yari, Mariacarolina Salerno, Daniela Vivenza, et al.. (2009). A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency. Journal of Endocrinological Investigation. 32(8). 653–658. 12 indexed citations
19.
Giordano, Mara, Michela Godi, Francesca Giacopelli, et al.. (2006). A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity. Molecular and Cellular Endocrinology. 249(1-2). 51–57. 12 indexed citations
20.
Giordano, Mara, Andrea Corrias, Simona Mellone, et al.. (2003). Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency. Clinical Genetics. 64(2). 142–147. 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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