D Falzetti

493 citations
21 papers · 298 · h-index 10

Impact in

  • Hematology top 10%
    • Acute Myeloid Leukemia Research
    • Chronic Myeloid Leukemia Treatments
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Chronic Lymphocytic Leukemia Research
    • Myeloproliferative Neoplasms: Diagnosis and Treatment

Papers in

    • Acute Myeloid Leukemia Research 12
    • Chronic Myeloid Leukemia Treatments 6
    • Genomic variations and chromosomal abnormalities 8
    • Chronic Lymphocytic Leukemia Research 6

D Falzetti

21 papers receiving 293 citations

Peers

D Falzetti
Comparison fields: 5 of 29
  • Hematology 109
  • Genetics 83
  • Pathology and Forensic Medicine 70
  • Genetics 69
  • Cancer Research 26
Replace Eva Lumbreras with:
Eva Lumbreras Spain
María T. Ardañaz Spain
Fiona Watkins United Kingdom
P. Mollevanger Netherlands
C. Grace United Kingdom
Claude Denis France
Jean‐Loup Huret France
Rika Kanezaki Japan
Masuzu Ueda Japan
Susana Bizarro Portugal
D Falzetti relative to Eva Lumbreras Spain Eva Lumbreras's profile →
Citations per field
00.5×1.5×1.9×
Eva Lumbreras · 1×
Citations per year

Countries citing papers authored by D Falzetti

Since Specialization
Citations

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

Fields of papers citing papers by D Falzetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside D Falzetti, 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 D Falzetti Line = papers co-authored together D Falzetti links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.
199952
2 199850
3 199844
4 199728
5 200125
6
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus.
199515
7 199814
8 199910
9 19999
10 20029
11 19969
12 20007
13 19996
14 19985
15 20024
16
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies.
19933
17
Metaphase FISH, microdissection, and multicolour FISH. Applications in haematology.
19993
18 19972
19 19981
20
Partial hemizygous deletion of ETV6 gene in two AML cases with an add(12)(p13)
19961

About D Falzetti

D Falzetti is a scholar working on Hematology, Genetics, Molecular Biology, Genetics and Plant Science, having authored 21 papers that have together received 298 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (12 papers), Genomic variations and chromosomal abnormalities (8 papers), Chronic Myeloid Leukemia Treatments (6 papers), Chronic Lymphocytic Leukemia Research (6 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers), Lymphoma Diagnosis and Treatment (2 papers) and RNA Interference and Gene Delivery (2 papers). The work is most often cited by research in Hematology (109 citations), Genetics (83 citations), Pathology and Forensic Medicine (70 citations), Genetics (69 citations) and Cancer Research (26 citations). D Falzetti has collaborated with scholars based in Italy, Belgium and Spain. Frequent co-authors include Cristina Mecucci, Herman Van den Berghe, Barbara Crescenzi, Roberta La Starza, Iwona Włodarska, Ana Aventín, Peter Marynen, Maria Paola Martelli, MF Martelli and Brunangelo Falini. Their work appears in journals such as Blood, Human Genetics, Genes Chromosomes and Cancer, Cytogenetic and Genome Research and Leukemia Research.

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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