Stefano Paolacci

1.0k total citations
53 papers, 706 citations indexed

About

Stefano Paolacci is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Stefano Paolacci has authored 53 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Oncology. Recurrent topics in Stefano Paolacci's work include Lymphatic System and Diseases (9 papers), Genomics and Rare Diseases (5 papers) and Vascular Malformations and Hemangiomas (5 papers). Stefano Paolacci is often cited by papers focused on Lymphatic System and Diseases (9 papers), Genomics and Rare Diseases (5 papers) and Vascular Malformations and Hemangiomas (5 papers). Stefano Paolacci collaborates with scholars based in Italy, Cyprus and Türkiye. Stefano Paolacci's co-authors include Matteo Bertelli, Elena Manara, Sandro Michelini, Tommaso Beccari, K Dhuli, Aysha Karim Kiani, Ján Miertuš, Domenico Pangallo, Astrit Dautaj and Paolo Enrico Maltese and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Gene.

In The Last Decade

Stefano Paolacci

52 papers receiving 687 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefano Paolacci Italy 15 199 125 124 117 79 53 706
Nur-Vaizura Mohamad Malaysia 15 296 1.5× 81 0.6× 187 1.5× 95 0.8× 68 0.9× 28 1.0k
Gareth Marlow New Zealand 14 552 2.8× 138 1.1× 55 0.4× 175 1.5× 88 1.1× 30 967
Hans‐Heinrich Henneicke‐von Zepelin Germany 18 204 1.0× 125 1.0× 65 0.5× 331 2.8× 51 0.6× 37 1.2k
Mehdi Barati Iran 15 193 1.0× 77 0.6× 95 0.8× 32 0.3× 64 0.8× 54 705
Ewa Maria Kratz Poland 19 360 1.8× 90 0.7× 104 0.8× 40 0.3× 49 0.6× 60 938
Anargyros N. Moulas Greece 15 193 1.0× 247 2.0× 53 0.4× 38 0.3× 67 0.8× 36 864
Fábio Hecht Brazil 15 297 1.5× 68 0.5× 81 0.7× 84 0.7× 55 0.7× 33 846
Jiunn‐Min Shieh Taiwan 18 365 1.8× 100 0.8× 101 0.8× 25 0.2× 57 0.7× 29 901
L. Thibault Canada 19 176 0.9× 186 1.5× 66 0.5× 84 0.7× 119 1.5× 45 844
Salim M. A. Bastaki United Arab Emirates 15 241 1.2× 71 0.6× 38 0.3× 108 0.9× 90 1.1× 43 862

Countries citing papers authored by Stefano Paolacci

Since Specialization
Citations

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

Fields of papers citing papers by Stefano Paolacci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Paolacci

This figure shows the co-authorship network connecting the top 25 collaborators of Stefano Paolacci. A scholar is included among the top collaborators of Stefano Paolacci 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 Paolacci. Stefano Paolacci 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.
Cannarella, Rossella, Rosita A. Condorelli, Andrea Bernini, et al.. (2023). Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series. International Journal of Molecular Sciences. 24(8). 7428–7428. 3 indexed citations
2.
Michelini, Sandro, Karen L. Herbst, Vincenza Precone, et al.. (2022). A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy. Journal of Personalized Medicine. 12(2). 268–268. 16 indexed citations
3.
Bonetti, G, Stefano Paolacci, Michele Samaja, et al.. (2022). Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways. International Journal of Molecular Sciences. 23(13). 7414–7414. 8 indexed citations
4.
Cecchin, S, Stefano Paolacci, Ján Miertuš, et al.. (2022). PacMAGI: A pipeline including accurate indel detection for the analysis of PacBio sequencing data applied to RPE65. Gene. 832. 146554–146554. 3 indexed citations
5.
Cristofoli, Francesca, Giulia Guerri, Roberta Maia de Castro Romanelli, et al.. (2021). Variant Selection and Interpretation: An Example of Modified VarSome Classifier of ACMG Guidelines in the Diagnostic Setting. Genes. 12(12). 1885–1885. 9 indexed citations
6.
Tripathi, Yamini Bhusan, Priyanka Mishra, Preeti Tripathi, et al.. (2021). Effect of a dietary supplement on the reduction of lymphedema-progression in mouse tail-cut model. SHILAP Revista de lepidopterología. 4 indexed citations
7.
Precone, Vincenza, Rossella Cannarella, Stefano Paolacci, et al.. (2021). Male Infertility Diagnosis: Improvement of Genetic Analysis Performance by the Introduction of Pre-Diagnostic Genes in a Next-Generation Sequencing Custom-Made Panel. Frontiers in Endocrinology. 11. 605237–605237. 18 indexed citations
8.
Ceccarini, Maria Rachele, Vincenza Precone, Elena Manara, et al.. (2021). A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa. Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 27(5). 1869–1880. 12 indexed citations
9.
Temel, Şehime Gülsün, Mahmut Çerkez Ergören, Elena Manara, et al.. (2020). Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome. European Journal of Human Genetics. 28(12). 1675–1680. 7 indexed citations
10.
Paolacci, Stefano, Raúl Mattassi, Giuseppe Marceddu, et al.. (2020). Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations. Journal of Clinical Medicine. 9(11). 3387–3387. 7 indexed citations
11.
Lorusso, Lorenzo, Vincenza Precone, Daniela Ferrari, et al.. (2020). Paraneoplastic Neurological Syndromes: Study of Prevalence in a Province of the Lombardy Region, Italy. Journal of Clinical Medicine. 9(10). 3105–3105. 4 indexed citations
12.
Vettori, Andrea, Stefano Paolacci, Paolo Enrico Maltese, et al.. (2020). Genetic Determinants of the Effects of Training on Muscle and Adipose Tissue Homeostasis in Obesity Associated with Lymphedema. Lymphatic Research and Biology. 19(4). 322–333. 6 indexed citations
13.
Severino, Mariasavina, Kerem Teralı, Elena Manara, et al.. (2020). Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder. Neurogenetics. 21(3). 179–186. 14 indexed citations
14.
Cannarella, Rossella, Stefano Paolacci, Federica Barbagallo, et al.. (2020). Next-generation sequencing. Asian Journal of Andrology. 23(1). 24–29. 23 indexed citations
15.
Precone, Vincenza, Stefano Paolacci, Pietro Chiurazzi, et al.. (2019). Cardiac conduction defects.. PubMed Central. 90(10-S). 20–29. 3 indexed citations
16.
Bertelli, Matteo, Aysha Karim Kiani, Stefano Paolacci, et al.. (2019). Hydroxytyrosol: A natural compound with promising pharmacological activities. Journal of Biotechnology. 309. 29–33. 187 indexed citations
17.
Martelli, Francesco, et al.. (2019). Electrical Stimulation in the Treatment of Lymphedema and Associated Skin Ulcers. Lymphatic Research and Biology. 18(3). 270–276. 7 indexed citations
18.
Bertelli, Matteo, Aysha Karim Kiani, Stefano Paolacci, et al.. (2019). Molecular pathways involved in lymphedema: Hydroxytyrosol as a candidate natural compound for treating the effects of lymph accumulation. Journal of Biotechnology. 308. 82–86. 11 indexed citations
19.
Paolacci, Stefano, Alessandra Zulian, Alice Bruson, et al.. (2019). Vascular anomalies: molecular bases, genetic testing and therapeutic approaches. International Angiology. 38(2). 157–170. 11 indexed citations
20.
Paolacci, Stefano, G. Pompucci, Barbara Paolini, et al.. (2019). Mendelian non-syndromic obesity.. PubMed. 90(10-S). 87–89. 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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