Ilaria Meloni

6.2k total citations
60 papers, 2.4k citations indexed

About

Ilaria Meloni is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Ilaria Meloni has authored 60 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 34 papers in Molecular Biology and 18 papers in Cognitive Neuroscience. Recurrent topics in Ilaria Meloni's work include Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (19 papers) and Autism Spectrum Disorder Research (18 papers). Ilaria Meloni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (19 papers) and Autism Spectrum Disorder Research (18 papers). Ilaria Meloni collaborates with scholars based in Italy, United States and Netherlands. Ilaria Meloni's co-authors include Alessandra Renieri, Ilaria Longo, Francesca Mari, Francesca Ariani, Joussef Hayek, Michele Zappella, Maria Antonietta Mencarelli, Mirella Bruttini, Chiara Pescucci and Ottavia Spiga and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Ilaria Meloni

59 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilaria Meloni Italy 29 1.7k 1.3k 759 166 136 60 2.4k
Francesca Ariani Italy 29 1.6k 1.0× 1.3k 1.0× 581 0.8× 219 1.3× 127 0.9× 70 2.4k
Ilaria Longo Italy 24 1.6k 1.0× 1.3k 0.9× 756 1.0× 274 1.7× 141 1.0× 41 2.3k
Maria Antonietta Mencarelli Italy 26 1.2k 0.7× 982 0.7× 354 0.5× 176 1.1× 92 0.7× 65 1.9k
Francesca Mari Italy 34 2.2k 1.3× 2.2k 1.6× 785 1.0× 453 2.7× 147 1.1× 103 3.8k
Mirella Bruttini Italy 22 777 0.5× 1.0k 0.8× 289 0.4× 294 1.8× 35 0.3× 40 1.6k
Chiara Pescucci Italy 19 745 0.4× 692 0.5× 224 0.3× 119 0.7× 37 0.3× 37 1.3k
Christophe Philippe France 30 1.6k 0.9× 1.5k 1.1× 309 0.4× 23 0.1× 56 0.4× 77 2.7k
Jaakko Ignatius Finland 29 1.1k 0.6× 1.6k 1.2× 213 0.3× 69 0.4× 27 0.2× 74 2.6k
Bert van der Zwaag Netherlands 23 704 0.4× 1.2k 0.9× 200 0.3× 98 0.6× 37 0.3× 44 2.2k
Patrick Calvas France 31 1.4k 0.9× 2.1k 1.6× 338 0.4× 110 0.7× 15 0.1× 104 3.9k

Countries citing papers authored by Ilaria Meloni

Since Specialization
Citations

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

Fields of papers citing papers by Ilaria Meloni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilaria Meloni

This figure shows the co-authorship network connecting the top 25 collaborators of Ilaria Meloni. A scholar is included among the top collaborators of Ilaria Meloni 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 Ilaria Meloni. Ilaria Meloni 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.
Quadalti, Corinne, Vito Antonio Baldassarro, Antonia Gurgone, et al.. (2024). A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling. Heliyon. 10(21). e40165–e40165.
2.
3.
Leoncini, Silvia, Diego Lopergolo, Roberto Canitano, et al.. (2023). Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey. Children. 10(9). 1442–1442. 2 indexed citations
4.
Alaverdian, Diana, et al.. (2021). The Phenomenon of Multidrug Resistance in Glioblastomas. Hematology/Oncology and Stem Cell Therapy. 15(2). 1–7. 18 indexed citations
5.
Croci, Susanna, Miriam Lucia Carriero, Katia Capitani, et al.. (2020). AAV-mediated FOXG1 gene editing in human Rett primary cells. European Journal of Human Genetics. 28(10). 1446–1458. 13 indexed citations
6.
Croci, Susanna, Miriam Lucia Carriero, Katia Capitani, et al.. (2020). High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot. European Journal of Human Genetics. 28(9). 1231–1242. 14 indexed citations
7.
Boggio, Elena, Caterina Lo Rizzo, Francesca Mari, et al.. (2016). Visual impairment in FOXG1-mutated individuals and mice. Neuroscience. 324. 496–508. 33 indexed citations
8.
Baldo, Chiara, Alessandra Renieri, Giuseppe Merla, et al.. (2016). The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks. Orphanet Journal of Rare Diseases. 11(1). 142–142. 27 indexed citations
9.
Signorini, Cinzia, Silvia Leoncini, Claudio De Felice, et al.. (2014). Redox Imbalance and Morphological Changes in Skin Fibroblasts in Typical Rett Syndrome. Oxidative Medicine and Cellular Longevity. 2014. 1–10. 46 indexed citations
10.
Rodriguez, Jayson, Ilaria Meloni, Sydney Ladd, et al.. (2010). Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3. American Journal of Medical Genetics Part A. 152A(3). 713–717. 13 indexed citations
11.
Uliana, Vera, Mafalda Mucciolo, Ilaria Meloni, et al.. (2010). Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2. Pediatric Nephrology. 26(5). 717–724. 23 indexed citations
12.
Mencarelli, Maria Antonietta, Tjitske Kleefstra, Eleni Katzaki, et al.. (2009). 14q12 Microdeletion syndrome and congenital variant of Rett syndrome. European Journal of Medical Genetics. 52(2-3). 148–152. 28 indexed citations
13.
Caselli, Rossella, Maria Antonietta Mencarelli, Filomena Tiziana Papa, et al.. (2008). Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation. American Journal of Medical Genetics Part A. 146A(9). 1195–1199. 19 indexed citations
14.
Sampieri, Katia, Maria Antonietta Mencarelli, Maria Carmela Epistolato, et al.. (2008). Genomic differences between retinoma and retinoblastoma. Acta Oncologica. 47(8). 1483–1492. 36 indexed citations
15.
Pescucci, Chiara, Rossella Caselli, Francesca Mari, et al.. (2006). The Italian XLMR bank: a clinical and molecular database. Human Mutation. 28(1). 13–18. 1 indexed citations
16.
Renieri, Alessandra, Chiara Pescucci, Ilaria Longo, et al.. (2005). Non‐syndromic X‐linked mental retardation: From a molecular to a clinical point of view. Journal of Cellular Physiology. 204(1). 8–20. 32 indexed citations
17.
Mari, Francesca, Rossella Caselli, Silvia Russo, et al.. (2005). Germline mosaicism in Rett syndrome identified by prenatal diagnosis. Clinical Genetics. 67(3). 258–260. 21 indexed citations
18.
Volti, S. Li, Teresio Avitabile, Giovanni Li Volti, et al.. (2002). Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian family. Graefe s Archive for Clinical and Experimental Ophthalmology. 240(9). 771–776. 8 indexed citations
19.
Meloni, Ilaria, Pietro Rubegni, G. De Aloe, et al.. (2001). Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11. Human Mutation. 18(1). 85–85. 37 indexed citations
20.
Seri, Marco, Michelangelo Savino, Domenico Bordo, et al.. (2001). Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene. Human Genetics. 110(2). 182–186. 36 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Francesca Ariani Breakdown of academic impact, for papers by Ilaria Longo Breakdown of academic impact, for papers by Maria Antonietta Mencarelli Breakdown of academic impact, for papers by Francesca Mari Breakdown of academic impact, for papers by Mirella Bruttini Breakdown of academic impact, for papers by Chiara Pescucci Breakdown of academic impact, for papers by Christophe Philippe Breakdown of academic impact, for papers by Jaakko Ignatius Breakdown of academic impact, for papers by Bert van der Zwaag Breakdown of academic impact, for papers by Patrick Calvas
Rankless by CCL
2026