Giulio Piluso

4.1k citations

83 papers · 2.5k indexed · h-index 26

Molecular Biology top 5%
Cardiology and Cardiovascular Medicine top 5%
Cellular and Molecular Neuroscience top 5%
Cell Biology top 5%
Genetics top 5%

Co-authors: Vincenzo Nigro Luisa Politano Angela Belsito Annibale Alessandro Puca Stefania Aurino Gerardo Nigro Mariz Vainzof Orlando Paciello
Topics: Muscle Physiology and Disorders (26 papers)Neurofibromatosis and Schwannoma Cases (14 papers)Neurogenetic and Muscular Disorders Research (11 papers)
Cited by: Genetics Molecular Biology Cellular and Molecular Neuroscience
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Nature Genetics
Partner nations: Italy United States Finland

In The Last Decade

Giulio Piluso

79 papers receiving 2.4k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical Efficacy of Selumetinib in Alleviating Neuropathic Pain Associated with Plexiform Neurofibroma: A Case Series 2025 ·Genes ·Giuseppina Miele,Irene Russo,(unknown),Silverio Perrotta,(unknown),Giulio Piluso,Mariarosa Anna Beatrice Melone,Claudia Santoro	0
2	Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18) 2025 ·Human Mutation ·(unknown),Francesca Nardecchia,Gerarda Cappuccio,(unknown),(unknown),S. Rahman,Gaetano Terrone,(unknown),(unknown),Michele Dei,Marco Trinchera,Vincenzo Leuzzi,Giulio Piluso,Vincenzo Nigro,Nicola Brunetti‐Pierri,Annalaura Torella	0
3	An atypical Aymé‐Gripp phenotype detected by exome sequencing 2023 ·American Journal of Medical Genetics Part A ·Martina Caiazza,(unknown),Emanuele Monda,(unknown),Augusto Esposito,Francesca Del Vecchio Blanco,Giulio Piluso,Vincenzo Nigro,Gioacchino Scarano,Giuseppe Limongelli	0
4	Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations 2023 ·Cancers ·(unknown),(unknown),Vincenzo Nigro,Silverio Perrotta,Giulio Piluso,Claudia Santoro	24
5	Next-Generation Sequencing (NGS) Analysis Illustrates the Phenotypic Variability of Collagen Type IV Nephropathies 2023 ·Genes ·Miriam Zacchia,Giovanna Capolongo,Francesca Del Vecchio Blanco,(unknown),Neha Gupta,(unknown),Rosa Maria Pollastro,(unknown),Giulio Piluso,(unknown),Annalaura Torella,Vincenzo Nigro,Alessandra Perna,Giovambattista Capasso,Francesco Trepiccione	1
6	Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically 2023 ·International Journal of Molecular Sciences ·Annalaura Torella,(unknown),(unknown),Francesca Del Vecchio Blanco,Esther Picillo,Luisa Politano,Vincenzo Nigro,Giulio Piluso	2
7	Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy 2023 ·Genes ·Emanuela Viggiano,Esther Picillo,Luigia Passamano,(unknown),Giulio Piluso,Marianna Scutifero,Annalaura Torella,Vincenzo Nigro,Luisa Politano	9
8	A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome 2023 ·Genes ·(unknown),Martina Caiazza,Antonella Farina,Gioacchino Scarano,(unknown),(unknown),Giuseppe Limongelli,Vincenzo Nigro,Giulio Piluso	1
9	Patients carrying Arg1809 substitution with no choroidal abnormalities: a further proof of a “Quasi-Incomplete” NF1 phenotype 2022 ·European Journal of Human Genetics ·Claudia Santoro,(unknown),Claudio Iovino,Giulio Piluso,Silverio Perrotta,Francesca Simonelli	2
10	A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort 2022 ·Cancers ·Rosina Paterra,Paola Bettinaglio,(unknown),Eleonora Mangano,(unknown),Claudia Cesaretti,(unknown),Roberta Bordoni,Claudia Santoro,Sabrina Avignone,Marco Moscatelli,Mariarosa Anna Beatrice Melone,Veronica Saletti,Giulio Piluso,Federica Natacci,Paola Riva,Marica Eoli	3
11	Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype 2022 ·Genes ·Filomena Napolitano,(unknown),Chiara Terracciano,(unknown),Maria Teresa Gentile,Giulio Piluso,Claudia Santoro,Davide Colavito,(unknown),Paolo De Blasiis,Simone Sampaolo,Simona Paladino,Mariarosa Anna Beatrice Melone	15
12	A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 2021 ·European Journal of Medical Genetics ·Claudia Santoro,(unknown),(unknown),Ferdinando Aliberti,Marco Carotenuto,(unknown),(unknown),Vincenzo Nigro,Silverio Perrotta,Giulio Piluso	4
13	Linked-Read Whole Genome Sequencing Solves a Double DMD Gene Rearrangement 2021 ·Genes ·(unknown),Annalaura Torella,Francesco Musacchia,Paola D′Ambrosio,(unknown),Francesca Del Vecchio Blanco,Giulio Piluso,Vincenzo Nigro	7
14	Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings 2021 ·Clinical Genetics ·Alessandra D’Amico,Carmen L. Rosano,Luca Pannone,Valentina Pinna,(unknown),Marialetizia Motta,Lorenzo Ugga,Paola Daniele,(unknown),(unknown),Maria Siano,Claudia Santoro,Giulio Piluso,Simone Martinelli,Pietro Strisciuglio,Alessandro De Luca,Marco Tartaglia,Daniela Melis	5
15	A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report 2020 ·BMC Neurology ·Claudia Santoro,Teresa Giugliano,Pia Bernardo,(unknown),Annalaura Torella,Francesca Del Vecchio Blanco,(unknown),Marco Carotenuto,Vincenzo Nigro,Giulio Piluso	8
16	Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 2019 ·Genes ·Teresa Giugliano,Claudia Santoro,Annalaura Torella,Francesca Del Vecchio Blanco,Anna Grandone,(unknown),Mariarosa Anna Beatrice Melone,Giulia Straccia,Daniela Melis,Vincenzo Piccolo,Giuseppe Limongelli,Salvatore Buono,Silverio Perrotta,Vincenzo Nigro,Giulio Piluso	29
17	Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1 2018 ·PLoS ONE ·Claudia Santoro,Teresa Giugliano,Markus Kraemer,Annalaura Torella,Jan Claudius Schwitalla,Mario Cirillo,Daniela Melis,Peter Berlit,Vincenzo Nigro,Silverio Perrotta,Giulio Piluso	22
18	A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects 2017 ·European Journal of Paediatric Neurology ·Gaetano Terrone,Giuseppina Vitiello,Rita Genesio,Alessandra D’Amico,(unknown),Lorenzo Ugga,Teresa Giugliano,Giulio Piluso,Lucio Nitsch,Nicola Brunetti‐Pierri,Ennio Del Giudice	3
19	Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype 2017 ·Clinical Genetics ·Claudia Santoro,Teresa Giugliano,Mariarosa Anna Beatrice Melone,Mario Cirillo,(unknown),Pia Bernardo,Giovanni Cirillo,Silverio Perrotta,Giulio Piluso	15
20	UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism 2017 ·American Journal of Medical Genetics Part A ·Teresa Giugliano,Claudia Santoro,Annalaura Torella,Francesca Del Vecchio Blanco,Pia Bernardo,Vincenzo Nigro,Giulio Piluso	8

About Giulio Piluso

Giulio Piluso is a scholar working on Genetics, Neurology and Molecular Biology, having authored 83 papers that have together received 2.5k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (26 papers), Neurofibromatosis and Schwannoma Cases (14 papers) and Neurogenetic and Muscular Disorders Research (11 papers). The work is most often cited by research in Genetics (316 citations), Molecular Biology (2.0k citations) and Cellular and Molecular Neuroscience (484 citations). Giulio Piluso has collaborated with scholars based in Italy, United States and Finland. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

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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