Paolo Catarsi

1.4k total citations
39 papers, 854 citations indexed

About

Paolo Catarsi is a scholar working on Genetics, Hematology and Rheumatology. According to data from OpenAlex, Paolo Catarsi has authored 39 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 16 papers in Hematology and 15 papers in Rheumatology. Recurrent topics in Paolo Catarsi's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (24 papers), Eosinophilic Disorders and Syndromes (14 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Paolo Catarsi is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (24 papers), Eosinophilic Disorders and Syndromes (14 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Paolo Catarsi collaborates with scholars based in Italy, United States and United Kingdom. Paolo Catarsi's co-authors include Vittorio Rosti, Gian Marco Ghiggeri, Rita Campanelli, Giovanni Barosi, Margherita Massa, Dmitry Lim, Valentina Poletto, Francesco Moccia, Francesco Perfumo and Roberto Ravazzolo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Paolo Catarsi

38 papers receiving 841 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paolo Catarsi Italy 14 355 248 205 180 163 39 854
Martin Siczkowski United Kingdom 16 293 0.8× 100 0.4× 36 0.2× 112 0.6× 204 1.3× 23 692
A Siddiqua United Kingdom 6 222 0.6× 30 0.1× 82 0.4× 49 0.3× 51 0.3× 7 616
Juan A. Ardura Spain 19 687 1.9× 33 0.1× 114 0.6× 54 0.3× 20 0.1× 35 1.1k
Matthew C. Havrda United States 16 712 2.0× 88 0.4× 17 0.1× 181 1.0× 34 0.2× 30 1.2k
Jinzhao Wang United States 16 570 1.6× 71 0.3× 48 0.2× 50 0.3× 24 0.1× 34 1.1k
Arancha R. Gortázar Spain 20 1.0k 2.8× 75 0.3× 72 0.4× 163 0.9× 28 0.2× 39 1.7k
Klaas Koop Netherlands 10 697 2.0× 161 0.6× 285 1.4× 31 0.2× 23 0.1× 21 1.1k
Antonio Maurizi Italy 16 949 2.7× 58 0.2× 59 0.3× 162 0.9× 29 0.2× 39 1.6k
Christopher Tweed United Kingdom 6 524 1.5× 38 0.2× 51 0.2× 47 0.3× 28 0.2× 7 880
Mattia Capulli Italy 22 889 2.5× 71 0.3× 42 0.2× 153 0.8× 28 0.2× 53 1.5k

Countries citing papers authored by Paolo Catarsi

Since Specialization
Citations

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

Fields of papers citing papers by Paolo Catarsi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paolo Catarsi

This figure shows the co-authorship network connecting the top 25 collaborators of Paolo Catarsi. A scholar is included among the top collaborators of Paolo Catarsi 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 Paolo Catarsi. Paolo Catarsi 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.
Croce, Stefania, Chiara Valsecchi, Elisa Lenta, et al.. (2024). Circulating Mesenchymal Stromal Cells in Patients with Infantile Hemangioma: Evaluation of Their Functional Capacity and Gene Expression Profile. Cells. 13(3). 254–254. 1 indexed citations
2.
Barosi, Giovanni, Paolo Catarsi, Rita Campanelli, et al.. (2023). VEGFA rs3025039 is associated with phenotype severity of myelofibrosis‐type megakaryocyte dysplasia. SHILAP Revista de lepidopterología. 4(3). 756–759. 1 indexed citations
3.
Campanelli, Rita, Adriana Carolei, Paolo Catarsi, et al.. (2022). Cells coexpressing both myeloid and endothelial markers are detectable in the spleen and bone marrow of patients with primary myelofibrosis. Experimental Hematology. 116. 26–29.
4.
Barosi, Giovanni, Rita Campanelli, Margherita Massa, et al.. (2022). Clonal Megakaryocyte Dysplasia with Isolated Thrombocytosis Is a Distinct Myeloproliferative Neoplasm Phenotype. Acta Haematologica. 146(1). 15–27. 3 indexed citations
5.
Villani, Laura, Vittorio Rosti, Margherita Massa, et al.. (2021). VEGFA rs3025020 Polymorphism Contributes to CALR-Mutation Susceptibility and Is Associated with Low Risk of Deep Vein Thrombosis in Primary Myelofibrosis. SHILAP Revista de lepidopterología. 5(4). e513–e520. 2 indexed citations
6.
Barosi, Giovanni, Vittorio Rosti, Margherita Massa, et al.. (2021). Clonal Megakaryocyte Dysplasia with Normal Blood Values Is a Distinct Myeloproliferative Neoplasm. Acta Haematologica. 145(1). 30–37. 3 indexed citations
7.
Barosi, Giovanni, Rita Campanelli, Paolo Catarsi, et al.. (2020). Plasma sIL-2Rα levels are associated with disease progression in myelofibrosis with JAK2V617F but not CALR mutation. Leukemia Research. 90. 106319–106319. 7 indexed citations
8.
Catarsi, Paolo. (2019). Digital PCR - Methods and Protocols. European Journal of Histochemistry. 63(4). 14 indexed citations
9.
Campanelli, Rita, Paolo Catarsi, Laura Villani, et al.. (2019). Constitutive STAT5 phosphorylation in CD34+ cells of patients with primary myelofibrosis: Correlation with driver mutation status and disease severity. PLoS ONE. 14(8). e0220189–e0220189. 4 indexed citations
10.
Barosi, Giovanni, Margherita Massa, Rita Campanelli, et al.. (2017). Primary myelofibrosis: Older age and high JAK2V617F allele burden are associated with elevated plasma high-sensitivity C-reactive protein levels and a phenotype of progressive disease. Leukemia Research. 60. 18–23. 27 indexed citations
11.
Zuccolo, Estella, Silvia Dragoni, Valentina Poletto, et al.. (2016). Arachidonic acid-evoked Ca2+ signals promote nitric oxide release and proliferation in human endothelial colony forming cells. Vascular Pharmacology. 87. 159–171. 52 indexed citations
12.
Catarsi, Paolo, Vittorio Rosti, Giacomo Morreale, et al.. (2015). JAK2 Exon 14 Skipping in Patients with Primary Myelofibrosis: A Minor Splice Variant Modulated by the JAK2-V617F Allele Burden. PLoS ONE. 10(1). e0116636–e0116636. 6 indexed citations
13.
Barosi, Giovanni, Rita Campanelli, Valentina Poletto, et al.. (2013). Decrease Of T Regulatory Cells In Patients With Myelofibrosis Receiving Ruxolitinib. Blood. 122(21). 4057–4057. 5 indexed citations
14.
Barosi, Giovanni, Valentina Poletto, Margherita Massa, et al.. (2013). JAK2 V617F Genotype Is a Strong Determinant of Blast Transformation in Primary Myelofibrosis. PLoS ONE. 8(3). e59791–e59791. 12 indexed citations
15.
Buduo, Christian A. Di, Rita Campanelli, Isabella Pallotta, et al.. (2013). Involvement of TGF 1 in autocrine regulation of proplatelet formation in healthy subjects and patients with primary myelofibrosis. Haematologica. 98(4). 514–517. 30 indexed citations
16.
Villani, Laura, Vittorio Rosti, Valentina Poletto, et al.. (2012). JAK2 46/1ハプロタイプは内臓静脈血栓症関連性BCR-ABL陰性の典型的骨髄増殖性腫瘍の素因となる. Leukemia Research. 36(1). 7–9. 1 indexed citations
17.
Giacopelli, Francesca, Angela Pistorio, Paolo Catarsi, et al.. (2004). Polymorphisms in the osteopontin promoter affect its transcriptional activity. Physiological Genomics. 20(1). 87–96. 111 indexed citations
18.
Ghiggeri, Gian Marco, Paolo Catarsi, Francesco Scolari, et al.. (2004). Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study. Clinical Therapeutics. 26(9). 1411–1418. 44 indexed citations
19.
Bruschi, Maurizio, Paolo Catarsi, Giovanni Candiano, et al.. (2003). Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis. Kidney International. 63(2). 686–695. 20 indexed citations
20.
Caridi, Gianluca, Roberta Bertelli, Alba Carrea, et al.. (2001). Prevalence, Genetics, and Clinical Features of Patients Carrying Podocin Mutations in Steroid-Resistant Nonfamilial Focal Segmental Glomerulosclerosis. Journal of the American Society of Nephrology. 12(12). 2742–2746. 140 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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