Claudio Panarello

694 total citations
30 papers, 455 citations indexed

About

Claudio Panarello is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Claudio Panarello has authored 30 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Hematology, 12 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Claudio Panarello's work include Acute Myeloid Leukemia Research (14 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Sarcoma Diagnosis and Treatment (6 papers). Claudio Panarello is often cited by papers focused on Acute Myeloid Leukemia Research (14 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Sarcoma Diagnosis and Treatment (6 papers). Claudio Panarello collaborates with scholars based in Italy and Sweden. Claudio Panarello's co-authors include Cristina Morerio, Cristina Rosanda, Maura Acquila, Elisa Tassano, Francesco Pasquali, Emanuela Maserati, Concetta Micalizzi, Laura Sainati, Mario Sessarego and Göran Stenman and has published in prestigious journals such as Cancer Research, Leukemia and Human Genetics.

In The Last Decade

Claudio Panarello

30 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claudio Panarello Italy 12 193 182 107 88 87 30 455
Cristina Rosanda Italy 12 193 1.0× 194 1.1× 73 0.7× 54 0.6× 78 0.9× 38 479
Cristina Morerio Italy 12 121 0.6× 187 1.0× 97 0.9× 63 0.7× 82 0.9× 29 384
Simonetta Kerim Italy 15 232 1.2× 144 0.8× 44 0.4× 29 0.3× 46 0.5× 34 521
Janet L. Lukacs United States 12 383 2.0× 386 2.1× 89 0.8× 145 1.6× 76 0.9× 27 680
Annet Simons Netherlands 17 153 0.8× 239 1.3× 149 1.4× 181 2.1× 145 1.7× 29 800
Shama L. van Zelderen‐Bhola Netherlands 9 437 2.3× 196 1.1× 51 0.5× 32 0.4× 78 0.9× 11 685
J. W. G. Janssen Germany 13 271 1.4× 234 1.3× 38 0.4× 71 0.8× 22 0.3× 18 564
Costanza Bosi Italy 13 385 2.0× 281 1.5× 98 0.9× 35 0.4× 28 0.3× 25 630
Joyce Murata‐Collins United States 12 175 0.9× 136 0.7× 24 0.2× 44 0.5× 70 0.8× 31 488
C Mecucci Italy 16 392 2.0× 293 1.6× 106 1.0× 51 0.6× 90 1.0× 35 765

Countries citing papers authored by Claudio Panarello

Since Specialization
Citations

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

Fields of papers citing papers by Claudio Panarello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudio Panarello

This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Panarello. A scholar is included among the top collaborators of Claudio Panarello 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 Claudio Panarello. Claudio Panarello 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.
Tassano, Elisa, et al.. (2010). Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma. Cancer Genetics and Cytogenetics. 203(2). 313–315. 4 indexed citations
2.
Tassano, Elisa, et al.. (2010). Cytogenetic characterization of a fibrous hamartoma of infancy with complex translocations. Cancer Genetics and Cytogenetics. 201(1). 66–69. 13 indexed citations
3.
Tassano, Elisa, et al.. (2010). MicroRNA‐125b‐1 and BLID upregulation resulting from a novel IGH translocation in childhood B‐Cell precursor acute lymphoblastic leukemia. Genes Chromosomes and Cancer. 49(8). 682–687. 26 indexed citations
4.
Morerio, Cristina, Paolo Nozza, Elisa Tassano, et al.. (2008). Differential diagnosis of lipoma‐like lipoblastoma. Pediatric Blood & Cancer. 52(1). 132–134. 19 indexed citations
5.
Porta, Giovanni, Elia Mattarucchi, Emanuela Maserati, et al.. (2007). Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR. Journal of Pediatric Hematology/Oncology. 29(3). 163–165. 4 indexed citations
6.
Morerio, Cristina, Elisa Tassano, Edoardo Lanino, et al.. (2006). Gain of 1q in pediatric myelodysplastic syndromes. Leukemia Research. 30(11). 1437–1441. 6 indexed citations
7.
Morerio, Cristina, et al.. (2005). MLL–MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia. Leukemia Research. 29(10). 1223–1226. 10 indexed citations
8.
Maserati, Emanuela, Antonella Minelli, Roberto Valli, et al.. (2005). Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies. Genes Chromosomes and Cancer. 45(4). 375–382. 37 indexed citations
9.
Morerio, Cristina, Cristina Rosanda, Edoardo Lanino, et al.. (2004). MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity. Cancer Genetics and Cytogenetics. 152(2). 108–112. 9 indexed citations
10.
Morerio, Cristina, Maura Acquila, Cristina Rosanda, et al.. (2004). t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia. Leukemia Research. 29(4). 467–470. 23 indexed citations
11.
Panarello, Claudio, Cristina Rosanda, & Cristina Morerio. (2002). Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia. Genes Chromosomes and Cancer. 35(3). 277–281. 27 indexed citations
12.
Morerio, Cristina, et al.. (2002). Is t(10;11)(p11.2;q23) involving MLL and ABI-1 genes associated with congenital acute monocytic leukemia?. Cancer Genetics and Cytogenetics. 139(1). 57–59. 9 indexed citations
13.
Morerio, Cristina, et al.. (2002). XY female with a dysgerminoma and no mutation in the coding sequence of the SRY gene. Cancer Genetics and Cytogenetics. 136(1). 58–61. 2 indexed citations
14.
Garaventa, Alberto, et al.. (2001). Early occurence of a secondary thyroid carcinoma in a child treated for Hodgkin disease. Medical and Pediatric Oncology. 36(3). 396–397. 4 indexed citations
15.
Minelli, Antonella, Cristina Morerio, Emanuela Maserati, et al.. (2001). Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia. Leukemia. 15(6). 971–975. 8 indexed citations
16.
Morerio, Cristina, Ivana Russo, Cristina Rosanda, et al.. (2001). 17q21–qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia. Cancer Genetics and Cytogenetics. 124(1). 12–15. 5 indexed citations
17.
Panarello, Claudio, Cristina Morerio, Ivana Russo, et al.. (2000). Full Cytogenetic Characterization of a New Neuroblastoma Cell Line with a Complex 17q Translocation. Cancer Genetics and Cytogenetics. 116(2). 124–132. 11 indexed citations
18.
Panarello, Claudio, Cristina Rosanda, Cristina Morerio, et al.. (1998). Lipoblastoma: A Case with t(7;8)(q31;q13). Cancer Genetics and Cytogenetics. 102(1). 12–14. 20 indexed citations
19.
Sessarego, Mario, et al.. (1988). Variant Philadelphia translocations in CML: Correlation with fragile sites. Cancer Genetics and Cytogenetics. 31(1). 105–112. 10 indexed citations
20.
Panarello, Claudio, et al.. (1983). G-Bands without pretreatment of slides, in chemically defined conditions. Human Genetics. 63(1). 63–66. 4 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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