Simona Petrucci

2.0k total citations · 1 hit paper
43 papers, 755 citations indexed

About

Simona Petrucci is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Simona Petrucci has authored 43 papers receiving a total of 755 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 10 papers in Molecular Biology and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Simona Petrucci's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological disorders and treatments (8 papers) and Cardiomyopathy and Myosin Studies (7 papers). Simona Petrucci is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological disorders and treatments (8 papers) and Cardiomyopathy and Myosin Studies (7 papers). Simona Petrucci collaborates with scholars based in Italy, United Kingdom and Canada. Simona Petrucci's co-authors include Enza Maria Valente, Monia Ginevrino, Antonio Pizzuti, Federica Consoli, Anna Rita Bentivoglio, Maria Piane, M. Manfredi, Carlo Di Bonaventura, Massimiliano Prencipe and Francesca Bonini and has published in prestigious journals such as PLoS ONE, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Simona Petrucci

36 papers receiving 750 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

European Neuroendocrine Tumor Society 2023 guidance paper for functioning pancreatic neuroendocrine tumour syndromes

2023 95 citations Johannes Hofland, Massimo Falconi et al. Journal of Neuroendocrinology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simona Petrucci Italy	16	453	195	135	135	132	43	755
Lee A. Shapiro United States	15	207 0.5×	174 0.9×	103 0.8×	76 0.6×	290 2.2×	26	835
Daniel Kremens United States	11	734 1.6×	241 1.2×	89 0.7×	64 0.5×	230 1.7×	26	993
Werner Poewe Austria	10	453 1.0×	118 0.6×	146 1.1×	96 0.7×	171 1.3×	18	695
Joachim Brumberg Germany	16	565 1.2×	304 1.6×	44 0.3×	69 0.5×	110 0.8×	47	889
Andres Deik United States	16	379 0.8×	188 1.0×	50 0.4×	224 1.7×	140 1.1×	33	722
Pierre Castelnau France	16	268 0.6×	160 0.8×	109 0.8×	79 0.6×	283 2.1×	50	826
Vasilios C. Constantinides Greece	15	345 0.8×	145 0.7×	38 0.3×	208 1.5×	78 0.6×	71	620
Bogdan Pintea Germany	15	193 0.4×	103 0.5×	87 0.6×	74 0.5×	87 0.7×	41	707
G M Szpak Poland	17	328 0.7×	141 0.7×	55 0.4×	210 1.6×	223 1.7×	41	829
Kurt Farrell United States	17	267 0.6×	164 0.8×	109 0.8×	209 1.5×	198 1.5×	46	754

Countries citing papers authored by Simona Petrucci

Since Specialization

Citations

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

Fields of papers citing papers by Simona Petrucci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simona Petrucci

This figure shows the co-authorship network connecting the top 25 collaborators of Simona Petrucci. A scholar is included among the top collaborators of Simona Petrucci 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 Petrucci. Simona Petrucci 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

Fabiani, Marco, Antonio Pizzuti, Aldo Germani, et al.. (2024). Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review. Preprints.org. 3 indexed citations

Mazzilli, Rossella, Simona Petrucci, Virginia Zamponi, et al.. (2024). Seminological, Hormonal and Ultrasonographic Features of Male Factor Infertility Due to Genetic Causes: Results from a Large Monocentric Retrospective Study. Journal of Clinical Medicine. 13(15). 4399–4399.

Fabiani, Marco, Giacomo Tini, Beatrice Musumeci, et al.. (2024). Reanalysis of Next-generation Sequencing Data in Patients With Hypertrophic Cardiomyopathy: Contribution of Spliceogenic MYBPC3 Variants in an Italian Cohort. Annals of Laboratory Medicine. 45(1). 96–100.

Fabiani, Marco, Antonio Pizzuti, Aldo Germani, et al.. (2024). Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review. International Journal of Molecular Sciences. 25(18). 9787–9787. 1 indexed citations

Germani, Aldo, et al.. (2023). Heterozygous Pathogenic Nonsense Variant in the ATM Gene in a Family with Unusually High Gastric Cancer Susceptibility. Biomedicines. 11(7). 2062–2062. 3 indexed citations

Fabiani, Marco, Erika Pagannone, Beatrice Musumeci, et al.. (2023). A Novel Nonsense Pathogenic TTN Variant Identified in a Patient with Severe Dilated Cardiomyopathy. Current Issues in Molecular Biology. 45(3). 2422–2430. 2 indexed citations

Faggiano, Antongiulio, Virginia Zamponi, Rossella Mazzilli, et al.. (2023). Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors. Genes. 14(9). 1782–1782. 1 indexed citations

Hofland, Johannes, Massimo Falconi, Emanuel Christ, et al.. (2023). European Neuroendocrine Tumor Society 2023 guidance paper for functioning pancreatic neuroendocrine tumour syndromes. Journal of Neuroendocrinology. 35(8). e13318–e13318. 95 indexed citations breakdown →

Piane, Maria, Aldo Germani, Marco Fabiani, et al.. (2022). A New SMAD4 Splice Site Variant in a Three-Generation Italian Family with Juvenile Polyposis Syndrome. Diagnostics. 12(11). 2684–2684. 4 indexed citations

10.

Sciacchitano, Salvatore, Maria Piane, Claudia De Vitis, et al.. (2022). Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?. Diagnostics. 12(12). 2997–2997. 3 indexed citations

11.

Raffa, Salvatore, Rita Mancini, Claudia Battista, et al.. (2022). From Survey Results to a Decision-Making Matrix for Strategic Planning in Healthcare: The Case of Clinical Pathways. International Journal of Environmental Research and Public Health. 19(13). 7806–7806.

12.

Piane, Maria, et al.. (2021). Genotype-Phenotype Correlations in Monogenic Parkinson Disease: A Review on Clinical and Molecular Findings. Frontiers in Neurology. 12. 648588–648588. 36 indexed citations

13.

Magrì, Damiano, Vittoria Mastromarino, Giovanna Gallo, et al.. (2020). Risk Stratification in Hypertrophic Cardiomyopathy. Insights from Genetic Analysis and Cardiopulmonary Exercise Testing. Journal of Clinical Medicine. 9(6). 1636–1636. 19 indexed citations

14.

Germani, Aldo, Simona Petrucci, Laura De Marchis, et al.. (2020). Beyond BRCA1 and BRCA2: Deleterious Variants in DNA Repair Pathway Genes in Italian Families with Breast/Ovarian and Pancreatic Cancers. Journal of Clinical Medicine. 9(9). 3003–3003. 7 indexed citations

15.

Carecchio, Miryam, Chiara Reale, Federica Invernizzi, et al.. (2016). DYT2 screening in early-onset isolated dystonia. European Journal of Paediatric Neurology. 21(2). 269–271. 9 indexed citations

16.

Petrucci, Simona, Federica Consoli, & Enza Maria Valente. (2014). Parkinson Disease Genetics: A “Continuum” from Mendelian to Multifactorial Inheritance. Current Molecular Medicine. 14(8). 1079–1088. 26 indexed citations

17.

Petrucci, Simona & Enza Maria Valente. (2013). Genetic Issues in the Diagnosis of Dystonias. Frontiers in Neurology. 4. 34–34. 15 indexed citations

18.

Onofrj, Marco, Sara Varanese, Laura Bonanni, et al.. (2013). Cohort study of prevalence and phenomenology of tremor in dementia with Lewy bodies. Journal of Neurology. 260(7). 1731–1742. 22 indexed citations

19.

Lapenta, Leonardo, Carlo Di Bonaventura, Jinane Fattouch, et al.. (2010). Focal epileptic seizure induced by transient hypoglycaemia in insulin‐treated diabetes. Epileptic Disorders. 12(1). 84–87. 16 indexed citations

20.

Fattouch, Jinane, Carlo Di Bonaventura, Giancarlo Di Gennaro, et al.. (2008). Electrical status epilepticus “invisible” to surface EEG in late‐onset Rasmussen encephalitis. Epileptic Disorders. 10(3). 219–222. 5 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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