Roberta Petillo

927 total citations
15 papers, 162 citations indexed

About

Roberta Petillo is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Roberta Petillo has authored 15 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Roberta Petillo's work include Muscle Physiology and Disorders (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Cardiac electrophysiology and arrhythmias (4 papers). Roberta Petillo is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Cardiac electrophysiology and arrhythmias (4 papers). Roberta Petillo collaborates with scholars based in Italy, France and Poland. Roberta Petillo's co-authors include Luisa Politano, Paola D′Ambrosio, Alberto Palladino, Andrea Antonio Papa, Marianna Scutifero, Manuela Ergoli, Gerardo Nigro, Luigia Passamano, Annalaura Torella and Antonella Taglia and has published in prestigious journals such as Human Mutation, Frontiers in Neurology and Genes.

In The Last Decade

Roberta Petillo

15 papers receiving 159 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberta Petillo Italy	8	133	77	34	31	27	15	162
Judit Balog Netherlands	6	215 1.6×	63 0.8×	23 0.7×	48 1.5×	51 1.9×	10	236
Vasantha Gowda United Kingdom	6	157 1.2×	57 0.7×	23 0.7×	75 2.4×	22 0.8×	15	204
Manuela Ergoli Italy	8	179 1.3×	66 0.9×	39 1.1×	32 1.0×	33 1.2×	12	205
Kyriaki Kekou Greece	8	148 1.1×	29 0.4×	77 2.3×	27 0.9×	28 1.0×	24	195
C. Cini United Kingdom	5	103 0.8×	40 0.5×	10 0.3×	35 1.1×	38 1.4×	5	148
Camille Dion France	6	130 1.0×	25 0.3×	34 1.0×	41 1.3×	24 0.9×	9	147
Rosanna Trovato Italy	6	146 1.1×	43 0.6×	27 0.8×	33 1.1×	79 2.9×	20	201
S. Makri France	5	140 1.1×	27 0.4×	23 0.7×	12 0.4×	43 1.6×	8	156
Nicolas Dondaine France	5	150 1.1×	31 0.4×	19 0.6×	21 0.7×	45 1.7×	5	196
Carrie Stephan United States	6	119 0.9×	49 0.6×	11 0.3×	35 1.1×	52 1.9×	13	136

Countries citing papers authored by Roberta Petillo

Since Specialization

Citations

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

Fields of papers citing papers by Roberta Petillo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Petillo

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Petillo. A scholar is included among the top collaborators of Roberta Petillo 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 Roberta Petillo. Roberta Petillo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Petillo, Roberta, et al.. (2023). Interatrial block as a first clinical presentation of atrial cardiomyopathy related to a novel LMNA variant: a case report. European Heart Journal - Case Reports. 7(12). ytad532–ytad532. 2 indexed citations

Siano, Maria, Ilaria Maggio, Roberta Petillo, et al.. (2022). De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review. Pediatric Reports. 14(1). 131–139. 16 indexed citations

Palladino, Alberto, Andrea Antonio Papa, Roberta Petillo, et al.. (2022). The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution. Genes. 13(2). 258–258. 10 indexed citations

Scutifero, Marianna, Michele Lanza, Roberta Petillo, et al.. (2022). Gender effect on onset, prevalence and surgical treatment of cataract in patients with Myotonic Dystrophy type 1.. PubMed. 41(3). 105–110. 2 indexed citations

Petillo, Roberta, Paola D′Ambrosio, Manuela Ergoli, et al.. (2020). CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita. Frontiers in Neurology. 11. 63–63. 5 indexed citations

D′Ambrosio, Paola, Roberta Petillo, Annalaura Torella, et al.. (2019). Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies.. PubMed. 38(2). 33–36. 3 indexed citations

Cascella, Raffaella, Claudia Strafella, Valerio Caputo, et al.. (2018). Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in SMCHD1 in a Family With FSHD. Frontiers in Neurology. 9. 1027–1027. 10 indexed citations

Altamura, Concetta, Sabrina Lucchiari, Giacomo P. Comi, et al.. (2018). The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel. Human Mutation. 39(9). 1273–1283. 14 indexed citations

Fontana, Paolo, Cristina Tortora, Roberta Petillo, et al.. (2017). Brachydactyly type E in an Italian family with 6p25 trisomy. European Journal of Medical Genetics. 60(3). 195–199. 4 indexed citations

10.

Papa, Andrea Antonio, Paola D′Ambrosio, Roberta Petillo, Alberto Palladino, & Luisa Politano. (2017). Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series. Intractable & Rare Diseases Research. 6(2). 95–101. 31 indexed citations

11.

Papa, Andrea Antonio, Anna Rago, Roberta Petillo, et al.. (2017). Is the epicardial left ventricular lead implantation an alternative approach to percutaneous attempt in patients with Steinert disease? A case report.. PubMed. 36(4). 213–217. 1 indexed citations

12.

Fontana, Paolo, et al.. (2016). A novel 5q11.2 microdeletion in a child with mild developmental delay and dysmorphic features. American Journal of Medical Genetics Part A. 170(9). 2445–2448. 1 indexed citations

13.

Palladino, Alberto, Paola D′Ambrosio, Andrea Antonio Papa, et al.. (2016). Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms.. PubMed. 35(3). 128–134. 8 indexed citations

14.

Petillo, Roberta, Paola D′Ambrosio, Annalaura Torella, et al.. (2015). Novel mutations in LMNA A/C gene and associated phenotypes.. PubMed Central. 34(2-3). 116–9. 18 indexed citations

15.

Taglia, Antonella, Roberta Petillo, Paola D′Ambrosio, et al.. (2015). Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene.. PubMed. 34(1). 9–13. 37 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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