Giulio Piluso

4.1k total citations
83 papers, 2.5k citations indexed

About

Giulio Piluso is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Giulio Piluso has authored 83 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 21 papers in Genetics and 17 papers in Neurology. Recurrent topics in Giulio Piluso's work include Muscle Physiology and Disorders (26 papers), Neurofibromatosis and Schwannoma Cases (14 papers) and Neurogenetic and Muscular Disorders Research (11 papers). Giulio Piluso is often cited by papers focused on Muscle Physiology and Disorders (26 papers), Neurofibromatosis and Schwannoma Cases (14 papers) and Neurogenetic and Muscular Disorders Research (11 papers). Giulio Piluso collaborates with scholars based in Italy, United States and Finland. Giulio Piluso's co-authors include Vincenzo Nigro, Luisa Politano, Angela Belsito, Annibale Alessandro Puca, Stefania Aurino, Gerardo Nigro, Mariz Vainzof, Orlando Paciello, Mayana Zatz and Eloisa De Sá Moreira and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Giulio Piluso

79 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
Giulio Piluso Italy 26 2.0k 516 484 423 405 83 2.5k
Monkol Lek United States 27 1.2k 0.6× 412 0.8× 379 0.8× 257 0.6× 827 2.0× 76 2.0k
Alban Vignaud France 28 1.4k 0.7× 218 0.4× 310 0.6× 314 0.7× 523 1.3× 53 2.0k
Sharon Keers United Kingdom 18 1.8k 0.9× 376 0.7× 553 1.1× 326 0.8× 134 0.3× 28 2.1k
Nigel F. Clarke Australia 29 1.8k 0.9× 1.1k 2.2× 343 0.7× 328 0.8× 294 0.7× 60 2.3k
C. Jimenez‐Mallebrera Spain 25 1.5k 0.7× 273 0.5× 256 0.5× 303 0.7× 177 0.4× 78 1.9k
Rita Barresi United Kingdom 19 1.8k 0.9× 542 1.1× 451 0.9× 497 1.2× 211 0.5× 36 2.1k
Rafaëlle Bernard France 20 2.3k 1.2× 237 0.5× 354 0.7× 367 0.9× 274 0.7× 54 2.8k
Yun Yuan China 27 1.8k 0.9× 344 0.7× 730 1.5× 237 0.6× 206 0.5× 272 3.0k
Belinda S. Cowling France 26 1.3k 0.7× 481 0.9× 383 0.8× 807 1.9× 207 0.5× 48 1.8k
Sasha Bogdanovich United States 21 1.9k 0.9× 295 0.6× 213 0.4× 384 0.9× 319 0.8× 33 2.3k

Countries citing papers authored by Giulio Piluso

Since Specialization
Citations

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

Fields of papers citing papers by Giulio Piluso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulio Piluso

This figure shows the co-authorship network connecting the top 25 collaborators of Giulio Piluso. A scholar is included among the top collaborators of Giulio Piluso 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 Giulio Piluso. Giulio Piluso 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.
Miele, Giuseppina, Irene Russo, Silverio Perrotta, et al.. (2025). Clinical Efficacy of Selumetinib in Alleviating Neuropathic Pain Associated with Plexiform Neurofibroma: A Case Series. Genes. 16(6). 645–645.
2.
Nardecchia, Francesca, Gerarda Cappuccio, S. Rahman, et al.. (2025). Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18). Human Mutation. 2025(1). 3531508–3531508.
3.
Caiazza, Martina, Emanuele Monda, Augusto Esposito, et al.. (2023). An atypical Aymé‐Gripp phenotype detected by exome sequencing. American Journal of Medical Genetics Part A. 194(1). 70–76.
4.
Nigro, Vincenzo, et al.. (2023). Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations. Cancers. 15(4). 1217–1217. 24 indexed citations
5.
Zacchia, Miriam, Giovanna Capolongo, Francesca Del Vecchio Blanco, et al.. (2023). Next-Generation Sequencing (NGS) Analysis Illustrates the Phenotypic Variability of Collagen Type IV Nephropathies. Genes. 14(3). 764–764. 1 indexed citations
6.
Torella, Annalaura, Francesca Del Vecchio Blanco, Esther Picillo, et al.. (2023). Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically. International Journal of Molecular Sciences. 24(11). 9241–9241. 2 indexed citations
7.
Viggiano, Emanuela, Esther Picillo, Luigia Passamano, et al.. (2023). Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy. Genes. 14(1). 214–214. 9 indexed citations
8.
Caiazza, Martina, Antonella Farina, Gioacchino Scarano, et al.. (2023). A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome. Genes. 15(1). 32–32. 1 indexed citations
9.
Santoro, Claudia, et al.. (2022). Patients carrying Arg1809 substitution with no choroidal abnormalities: a further proof of a “Quasi-Incomplete” NF1 phenotype. European Journal of Human Genetics. 31(2). 136–137. 2 indexed citations
10.
Paterra, Rosina, Paola Bettinaglio, Eleonora Mangano, et al.. (2022). A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers. 15(1). 59–59. 3 indexed citations
11.
Napolitano, Filomena, Chiara Terracciano, Maria Teresa Gentile, et al.. (2022). Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype. Genes. 13(7). 1130–1130. 15 indexed citations
12.
Santoro, Claudia, Ferdinando Aliberti, Marco Carotenuto, et al.. (2021). A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome. European Journal of Medical Genetics. 64(5). 104190–104190. 4 indexed citations
13.
Torella, Annalaura, Francesco Musacchia, Paola D′Ambrosio, et al.. (2021). Linked-Read Whole Genome Sequencing Solves a Double DMD Gene Rearrangement. Genes. 12(2). 133–133. 7 indexed citations
14.
D’Amico, Alessandra, Carmen L. Rosano, Luca Pannone, et al.. (2021). Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings. Clinical Genetics. 100(5). 563–572. 5 indexed citations
15.
Santoro, Claudia, Teresa Giugliano, Pia Bernardo, et al.. (2020). A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report. BMC Neurology. 20(1). 327–327. 8 indexed citations
16.
Giugliano, Teresa, Claudia Santoro, Annalaura Torella, et al.. (2019). Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders. Genes. 10(8). 580–580. 29 indexed citations
17.
Santoro, Claudia, Teresa Giugliano, Markus Kraemer, et al.. (2018). Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. PLoS ONE. 13(7). e0200446–e0200446. 22 indexed citations
18.
Terrone, Gaetano, Giuseppina Vitiello, Rita Genesio, et al.. (2017). A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. European Journal of Paediatric Neurology. 21(6). 902–906. 3 indexed citations
19.
Santoro, Claudia, Teresa Giugliano, Mariarosa Anna Beatrice Melone, et al.. (2017). Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype. Clinical Genetics. 93(1). 138–143. 15 indexed citations
20.
Giugliano, Teresa, Claudia Santoro, Annalaura Torella, et al.. (2017). UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism. American Journal of Medical Genetics Part A. 176(3). 722–726. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Monkol Lek Breakdown of academic impact, for papers by Alban Vignaud Breakdown of academic impact, for papers by Sharon Keers Breakdown of academic impact, for papers by Nigel F. Clarke Breakdown of academic impact, for papers by C. Jimenez‐Mallebrera Breakdown of academic impact, for papers by Rita Barresi Breakdown of academic impact, for papers by Rafaëlle Bernard Breakdown of academic impact, for papers by Yun Yuan Breakdown of academic impact, for papers by Belinda S. Cowling Breakdown of academic impact, for papers by Sasha Bogdanovich
Rankless by CCL
2026