C Barletta

551 citations
28 papers · 452 indexed · h-index 12

Impact in

  • Hematology top 10%
    • Acute Myeloid Leukemia Research
    • Chronic Myeloid Leukemia Treatments
    • Chronic Lymphocytic Leukemia Research
    • Genomic variations and chromosomal abnormalities

Papers in

C Barletta

28 papers receiving 439 citations

Peers

C Barletta
Comparison fields: 5 of 61
  • Hematology 110
  • Genetics 64
  • Genetics 114
  • Molecular Biology 268
  • Immunology 66
Replace P. Mollevanger with:
P. Mollevanger Netherlands
Laëtitia Gressin France
Francesco Acquadro Spain
Maia V. Ouspenskaia United States
T. W. J. Hustinx Netherlands
Martine Guillier France
Marie Trková Czechia
Hélia Neves Portugal
Caterina Tatarelli Italy
Ton de Wit Netherlands
C Barletta relative to P. Mollevanger Netherlands P. Mollevanger's profile →
Citations per field
00.5×
P. Mollevanger · 1×
Citations per year

Countries citing papers authored by C Barletta

Since Specialization
Citations

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

Fields of papers citing papers by C Barletta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside C Barletta, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C Barletta Line = papers co-authored together C Barletta links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20251
2
Cytogenetic, molecular and phenotypic characterization of the newly established renal carcinoma cell line KJ29. Evidence of translocations for chromosomes 1 and 3.
19966
3
Multiple genetic lesions in solid tumors: relevance to diagnosis, prognosis, and molecular mechanisms.
19961
4 199454
5
Evolutionary conservation of the EPS8 gene and its mapping to human chromosome 12q23-q24.
199419
6 199374
7
C-MYB activation and the pathogenesis of ovarian cancer.
19928
8
Endocrine abortion in assisted reproduction technologies (ART).
19921
9 19918
10 199141
11
Chromosome locations of the MYB related genes, AMYB and BMYB.
199112
12
Segregation analysis of autosomal fragile sites in three families with the fragile X chromosome.
19914
13 199016
14 199013
15 19903
16 19902
17 198910
18 19891
19 19866
20
Partial deletion of the long arm of chromosome 17 in acute promyelocitic leukemia.
19851

About C Barletta

C Barletta is a scholar working on Hematology, Developmental Biology, Genetics, Genetics and Immunology, having authored 28 papers that have together received 452 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Acute Myeloid Leukemia Research (4 papers), T-cell and Retrovirus Studies (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Chronic Myeloid Leukemia Treatments (3 papers), Acute Lymphoblastic Leukemia research (3 papers), Virus-based gene therapy research (2 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Hematology (110 citations), Genetics (64 citations), Genetics (114 citations), Molecular Biology (268 citations) and Immunology (66 citations). C Barletta has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Riccardo Dalla‐Favera, Pier Giuseppe Pelicci, Lawrence C. Kenyon, C Peschle, Stephen D. Smith, Ugo Testa, M Valtieri, Teresa Druck, Beverly J. Lange and Margaret Nieborowska-Skorska. Their work appears in journals such as Blood, Genomics, Genes Chromosomes and Cancer, Leukemia Research and International Journal of Molecular Sciences.

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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