Caterina Matteucci

1.2k total citations
49 papers, 604 citations indexed

About

Caterina Matteucci is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Caterina Matteucci has authored 49 papers receiving a total of 604 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Hematology, 19 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in Caterina Matteucci's work include Acute Myeloid Leukemia Research (25 papers), Acute Lymphoblastic Leukemia research (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Caterina Matteucci is often cited by papers focused on Acute Myeloid Leukemia Research (25 papers), Acute Lymphoblastic Leukemia research (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Caterina Matteucci collaborates with scholars based in Italy, Belgium and United Kingdom. Caterina Matteucci's co-authors include Cristina Mecucci, Roberta La Starza, Barbara Crescenzi, Maria Paola Martelli, Gianluca Barba, Valentina Pierini, Paolo Gorello, Sabina Chiaretti, Lei Gao and Massimo Fiorilli and has published in prestigious journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Caterina Matteucci

49 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caterina Matteucci Italy 15 306 219 168 117 114 49 604
Susanna Fenu Italy 15 794 2.6× 510 2.3× 203 1.2× 160 1.4× 52 0.5× 30 929
Jinjun Cheng United States 10 155 0.5× 171 0.8× 78 0.5× 51 0.4× 54 0.5× 24 377
Hagen Graf Einsiedel Germany 7 195 0.6× 233 1.1× 237 1.4× 35 0.3× 41 0.4× 13 548
WE Fibbe Netherlands 10 476 1.6× 161 0.7× 78 0.5× 101 0.9× 31 0.3× 10 742
Naoko Watanabe‐Okochi Japan 15 446 1.5× 481 2.2× 56 0.3× 139 1.2× 27 0.2× 31 809
Jun Mo United States 10 168 0.5× 235 1.1× 46 0.3× 49 0.4× 32 0.3× 26 480
N. Horvath United States 9 417 1.4× 126 0.6× 36 0.2× 95 0.8× 120 1.1× 16 660
Sebastian Vosberg Germany 10 288 0.9× 227 1.0× 154 0.9× 75 0.6× 45 0.4× 20 570
J. Treleaven United Kingdom 10 354 1.2× 177 0.8× 156 0.9× 135 1.2× 141 1.2× 17 636
MM Le Beau United States 8 401 1.3× 267 1.2× 189 1.1× 112 1.0× 77 0.7× 8 597

Countries citing papers authored by Caterina Matteucci

Since Specialization
Citations

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

Fields of papers citing papers by Caterina Matteucci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caterina Matteucci

This figure shows the co-authorship network connecting the top 25 collaborators of Caterina Matteucci. A scholar is included among the top collaborators of Caterina Matteucci 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 Caterina Matteucci. Caterina Matteucci 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.
Pierini, Valentina, Barbara Crescenzi, Caterina Matteucci, et al.. (2024). Epigenetic Modeling of Jumping Translocations of 1q Heterochromatin in Acute Myeloid Leukemia After 5'‐Azacytidine Treatment. Genes Chromosomes and Cancer. 63(11). e70013–e70013. 1 indexed citations
2.
Gorello, Paolo, Roberto Maria Pellegrino, Hovirag Lancioni, et al.. (2023). Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes. International Journal of Molecular Sciences. 24(3). 2529–2529. 4 indexed citations
3.
Guglielmini, Giuseppe, Emanuela Falcinelli, Loredana Bury, et al.. (2021). Germline <i>GATA2</i> variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation. Haematologica. 107(5). 1072–1085. 7 indexed citations
4.
Giacomo, Danika Di, Valentina Pierini, Roberta La Starza, et al.. (2021). Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement. Annals of Hematology. 101(2). 297–307. 8 indexed citations
5.
Lancioni, Hovirag, Roberta La Starza, Irene Cardinali, et al.. (2020). Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study. PLoS ONE. 15(10). e0240632–e0240632. 3 indexed citations
6.
Starza, Roberta La, Lorenza Pastorino, Elisabetta Albi, et al.. (2018). Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin. Molecular Cytogenetics. 11(1). 6–6. 3 indexed citations
7.
Starza, Roberta La, Gianluca Barba, Sofie Demeyer, et al.. (2016). Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia. Haematologica. 101(8). 951–958. 14 indexed citations
8.
Giacomo, Danika Di, et al.. (2014). The GNAS1 gene in myelodysplastic syndromes (MDS). Leukemia Research. 38(7). 804–807. 3 indexed citations
9.
Pierini, Valentina, Roberta La Starza, Gianluca Barba, et al.. (2011). Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. Cancer Genetics. 204(10). 563–568. 1 indexed citations
10.
Gorello, Paolo, Roberta La Starza, Sabina Chiaretti, et al.. (2010). Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults. Haematologica. 95(1). 79–86. 32 indexed citations
11.
Starza, Roberta La, Caterina Matteucci, Paolo Gorello, et al.. (2010). NPM1 Deletion Is Associated with Gross Chromosomal Rearrangements in Leukemia. PLoS ONE. 5(9). e12855–e12855. 10 indexed citations
12.
Starza, Roberta La, Barbara Crescenzi, Valentina Pierini, et al.. (2007). A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma. Cancer Genetics and Cytogenetics. 175(1). 73–76. 18 indexed citations
13.
Rosati, Roberto, Gianluca Barba, Paolo Gorello, et al.. (2007). Cryptic chromosome 9q34 deletion generates TAF-I /CAN and TAF-I /CAN fusion transcripts in acute myeloid leukemia. Haematologica. 92(2). 232–235. 40 indexed citations
14.
Crescenzi, Barbara, Roberta La Starza, Chiara Nozzoli, et al.. (2007). Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia. Cancer Genetics and Cytogenetics. 176(1). 67–71. 10 indexed citations
15.
Starza, Roberta La, Gianluca Barba, Caterina Matteucci, et al.. (2006). Chronic lymphocytic leukaemia. Leukemia Research. 30(12). 1569–1572. 3 indexed citations
16.
Starza, Roberta La, Anna Aventı́n, Caterina Matteucci, et al.. (2006). Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia. Leukemia. 20(6). 958–964. 6 indexed citations
17.
Matteucci, Caterina, Roberta La Starza, Barbara Crescenzi, et al.. (2002). Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line. Cancer Genetics and Cytogenetics. 135(1). 28–34. 9 indexed citations
18.
Falzetti, D, Joris Vermeesch, Caterina Matteucci, et al.. (2000). Microdissection and FISH Investigations in Acute Myeloid Leukemia. Cancer Genetics and Cytogenetics. 118(1). 28–34. 7 indexed citations
19.
Starza, Roberta La, Iwona Włodarska, Caterina Matteucci, et al.. (1998). Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML‐M1). Genes Chromosomes and Cancer. 23(1). 10–15. 1 indexed citations
20.
Angioni, Adriano, Roberta La Starza, Cristina Mecucci, et al.. (1998). Interstitial Insertion of AF10 into the ALL1 Gene in a Case of Infant Acute Lymphoblastic Leukemia. Cancer Genetics and Cytogenetics. 107(2). 107–110. 14 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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