Stefano Petrocchi

434 total citations
15 papers, 236 citations indexed

About

Stefano Petrocchi is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Stefano Petrocchi has authored 15 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Stefano Petrocchi's work include Genomic variations and chromosomal abnormalities (6 papers), Cystic Fibrosis Research Advances (3 papers) and Genomics and Chromatin Dynamics (2 papers). Stefano Petrocchi is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Cystic Fibrosis Research Advances (3 papers) and Genomics and Chromatin Dynamics (2 papers). Stefano Petrocchi collaborates with scholars based in Italy and United States. Stefano Petrocchi's co-authors include Adriano Angioni, M. Cristina Digilio, Pietro Sirleto, Francesca Romana Lepri, Elisa Pisaneschi, Cecilia Surace, Rossella Capolino, Gemma D’Elia, Leonardo Ciocca and Bruno Dallapiccola and has published in prestigious journals such as Frontiers in Immunology, Archives of Disease in Childhood and Molecular Medicine.

In The Last Decade

Stefano Petrocchi

14 papers receiving 211 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefano Petrocchi Italy	8	129	84	31	22	19	15	236
Aline Receveur France	9	109 0.8×	81 1.0×	20 0.6×	10 0.5×	29 1.5×	22	200
Neda Zadeh United States	7	141 1.1×	152 1.8×	25 0.8×	20 0.9×	6 0.3×	12	253
Ken L. Jones United States	6	96 0.7×	154 1.8×	38 1.2×	28 1.3×	17 0.9×	7	284
Konstantina Kosma Greece	10	137 1.1×	130 1.5×	21 0.7×	24 1.1×	17 0.9×	30	288
Cynthia Lim United States	5	145 1.1×	126 1.5×	24 0.8×	8 0.4×	34 1.8×	9	231
Özge Özalp Yüreğir Türkiye	8	133 1.0×	137 1.6×	27 0.9×	12 0.5×	17 0.9×	20	288
Angeline Lai Singapore	10	133 1.0×	152 1.8×	67 2.2×	17 0.8×	7 0.4×	31	349
Nils Koelling United Kingdom	7	92 0.7×	137 1.6×	12 0.4×	12 0.5×	11 0.6×	10	214
Alina Khromykh United States	10	164 1.3×	202 2.4×	42 1.4×	30 1.4×	8 0.4×	13	367
M. Elizabeth McCready Canada	10	120 0.9×	80 1.0×	7 0.2×	25 1.1×	14 0.7×	25	254

Countries citing papers authored by Stefano Petrocchi

Since Specialization

Citations

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

Fields of papers citing papers by Stefano Petrocchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Petrocchi

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Falco, Alessandro De, Daniele De Brasi, Stefano Petrocchi, et al.. (2023). A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes. 14(1). 119–119. 2 indexed citations

Rossi, Marianna Nicoletta, Silvia Federici, Chiara Passarelli, et al.. (2022). Identification of a Novel Mutation in TNFAIP3 in a Family With Poly-Autoimmunity. Frontiers in Immunology. 13. 804401–804401. 15 indexed citations

Sofia, Valentina, Letizia Da Sacco, Cecilia Surace, et al.. (2016). Extensive Molecular Analysis Suggested the Strong Genetic Heterogeneity of Idiopathic Chronic Pancreatitis. Molecular Medicine. 22(1). 300–309. 18 indexed citations

Cifaldi, Loredana, Rita Maria Pinto, Maurizio Caniglia, et al.. (2016). NK cell effector functions in a Chédiak-Higashi patient undergoing cord blood transplantation: Effects of in vitro treatment with IL-2. Immunology Letters. 180. 46–53. 5 indexed citations

Sofia, Valentina, Cecilia Surace, Fabio Majo, et al.. (2015). Relationship between CFTR and CTRC Variants and the Clinical Phenotype in Late-Onset Cystic Fibrosis Disease with Chronic Pancreatitis. Journal of Molecular Diagnostics. 17(2). 171–178. 6 indexed citations

Pisaneschi, Elisa, Pietro Sirleto, Francesca Romana Lepri, et al.. (2015). CHARGE syndrome due to deletion of region upstream of CHD7 gene START codon. BMC Medical Genetics. 16(1). 78–78. 3 indexed citations

Ciocca, Leonardo, M. Cristina Digilio, Gemma D’Elia, et al.. (2015). Hypoplastic left heart syndrome and 21q22.3 deletion. American Journal of Medical Genetics Part A. 167(3). 579–586. 19 indexed citations

Dentici, Maria Lisa, Francesca Romana Lepri, Maria Gnazzo, et al.. (2014). Kabuki syndrome: clinical and molecular diagnosis in the first year of life. Archives of Disease in Childhood. 100(2). 158–164. 62 indexed citations

Surace, Cecilia, Francesco Berardinelli, Andrea Masotti, et al.. (2014). Telomere shortening and telomere position effect in mild ring 17 syndrome. Epigenetics & Chromatin. 7(1). 1–1. 59 indexed citations

10.

Pontrelli, Giuseppe, Simona Cappelletti, Dianela Claps, et al.. (2014). Epilepsy in Patients With Duplications of Chromosome 14 Harboring FOXG1. Pediatric Neurology. 50(5). 530–535. 15 indexed citations

11.

Sirleto, Pietro, Cecilia Surace, Federico Alghisi, et al.. (2011). Characterization of a novel isolated deletion of the exon 3 within the CFTR gene: Relevance for phenotypic expression and genetic counseling. Clinical Biochemistry. 44(10-11). 799–803. 1 indexed citations

12.

Roberti, María P., Cecilia Surace, M. Cristina Digilio, et al.. (2011). Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome. Orphanet Journal of Rare Diseases. 6(1). 17–17. 9 indexed citations

13.

Alghisi, Federico, Stefano Petrocchi, Cecilia Surace, et al.. (2010). Clinical hallmarks and genetic polymorphisms in the CFTR gene contribute to the disclosure of the A1006E mutation. Clinical and investigative medicine. 33(4). E234–E239. 1 indexed citations

14.

Surace, Cecilia, Pietro Sirleto, Gemma D’Elia, et al.. (2009). Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints location. Clinical Genetics. 76(3). 256–262. 21 indexed citations

15.

Petrocchi, Stefano, et al.. (2004). Limes linguistico e limes artistico nella Roma del Rinascimento. Iris (Roma Tre University). 99–137.

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