Letizia Longo

1.9k total citations
19 papers, 1.5k citations indexed

About

Letizia Longo is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Letizia Longo has authored 19 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Hematology and 3 papers in Genetics. Recurrent topics in Letizia Longo's work include Acute Myeloid Leukemia Research (9 papers), Retinoids in leukemia and cellular processes (9 papers) and Renal and related cancers (3 papers). Letizia Longo is often cited by papers focused on Acute Myeloid Leukemia Research (9 papers), Retinoids in leukemia and cellular processes (9 papers) and Renal and related cancers (3 papers). Letizia Longo collaborates with scholars based in Italy, United Kingdom and United States. Letizia Longo's co-authors include Andrea Biondi, F Grignani, Myriam Alcalay, Pier Giuseppe Pelicci, Emilio Donti, Amedea Mencarelli, PP Pandolfi, Alessandro Rambaldi, M Fagioli and P P Pandolfi and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Letizia Longo

19 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Letizia Longo Italy	15	1.2k	793	282	183	163	19	1.5k
Rohini C. Vyas United States	9	1.2k 1.0×	621 0.8×	301 1.1×	248 1.4×	122 0.7×	11	1.4k
PP Pandolfi Italy	12	1.3k 1.1×	1.1k 1.3×	180 0.6×	249 1.4×	220 1.3×	19	1.6k
Z Chen China	9	957 0.8×	677 0.9×	212 0.8×	99 0.5×	110 0.7×	21	1.2k
Seppo Pakkala Finland	15	451 0.4×	285 0.4×	220 0.8×	53 0.3×	78 0.5×	33	757
Evelio Perez‐Albuerne United States	10	380 0.3×	126 0.2×	138 0.5×	27 0.1×	27 0.2×	14	721
Charles P. Lerner United States	10	607 0.5×	297 0.4×	239 0.8×	10 0.1×	37 0.2×	23	1.0k
Naruyoshi Suwabe Japan	15	917 0.7×	365 0.5×	91 0.3×	11 0.1×	22 0.1×	23	1.3k
Vladimír Divoký Czechia	22	678 0.6×	755 1.0×	155 0.5×	7 0.0×	68 0.4×	78	1.6k
T Umiel United States	13	260 0.2×	78 0.1×	146 0.5×	23 0.1×	45 0.3×	27	642
G Mastroberardino Italy	15	419 0.3×	307 0.4×	86 0.3×	12 0.1×	22 0.1×	37	886

Countries citing papers authored by Letizia Longo

Since Specialization

Citations

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

Fields of papers citing papers by Letizia Longo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Letizia Longo

This figure shows the co-authorship network connecting the top 25 collaborators of Letizia Longo. A scholar is included among the top collaborators of Letizia Longo 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 Letizia Longo. Letizia Longo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Longo, Letizia. (2002). Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal. The EMBO Journal. 21(16). 4229–4239. 119 indexed citations

Longo, Letizia, et al.. (2000). PCR amplification of the 16S mitochondrial gene of Zoanthus sociatus (Zoanthidea, Anthozoa) using heterologous primers. 2 indexed citations

Longo, Letizia, Anne E. Bygrave, Frank Grosveld, & Pier Paolo Pandolfi. (1997). The chromosome make-up of mouse embryonic stem cells is predictive of somatic and germ cell chimaerism. Transgenic Research. 6(5). 321–328. 131 indexed citations

Cristofano, Antonio Di, Maria Strazzullo, Letizia Longo, & Girolama La Mantia. (1995). Characterization and genomic mapping of the ZNF80 locus: expression of this zinc-finger gene is driven by a solitary LTR of ERV9 endogenous retrovrial family. Nucleic Acids Research. 23(15). 2823–2830. 64 indexed citations

Lafage‐Pochitaloff, Mårina, Myriam Alcalay, Letizia Longo, et al.. (1995). Acute promyelocytic leukemia cases with nonreciprocal PML/RARa or RARa/PML fusion genes. Blood. 85(5). 1169–1174. 59 indexed citations

Grignani, F, M Fagioli, Myriam Alcalay, et al.. (1994). Acute promyelocytic leukemia: from genetics to treatment. Blood. 83(1). 10–25. 400 indexed citations

Bessler, Monica, Peter Hillmen, Letizia Longo, Lucio Luzzatto, & Philip J. Mason. (1994). Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21. Human Molecular Genetics. 3(5). 751–757. 56 indexed citations

Trecca, Dino, Letizia Longo, Andrea Biondi, et al.. (1994). Analysis of p53 gene mutations in acute myeloid leukemia. American Journal of Hematology. 46(4). 304–309. 34 indexed citations

Longo, Letizia, Dino Trecca, Andrea Biondi, et al.. (1993). Frequency of RAS and p53 Mutations in Acute Promyelocytic Leukemias. Leukemia & lymphoma. 11(5-6). 405–410. 30 indexed citations

10.

Lanfrancone, Luisa, Gina Pengue, P P Pandolfi, et al.. (1992). Structural and functional organization of the HF.10 human zinc finger gene (ZNF35) located on chromosome 3p21–p22. Genomics. 12(4). 720–728. 15 indexed citations

11.

Alcalay, Myriam, Letizia Longo, M Fagioli, et al.. (1992). Molecular genetics of the t(15;17) of acute promyelocytic leukemia (APPL).. PubMed. 6 Suppl 3. 120S–122S. 6 indexed citations

12.

Biondi, Andrea, Myriam Alcalay, PP Pandolfi, et al.. (1991). RAR-alpha gene rearrangements as a genetic marker for diagnosis and monitoring in acute promyelocytic leukemia. Blood. 77(7). 1418–1422. 4 indexed citations

13.

Biondi, Andrea, Alessandro Rambaldi, Myriam Alcalay, et al.. (1991). RAR-alpha gene rearrangements as a genetic marker for diagnosis and monitoring in acute promyelocytic leukemia. Blood. 77(7). 1418–1422. 85 indexed citations

14.

Alcalay, Myriam, D Zangrilli, P P Pandolfi, et al.. (1991). Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus.. Proceedings of the National Academy of Sciences. 88(5). 1977–1981. 215 indexed citations

15.

Longo, Letizia, Emilio Donti, Amedea Mencarelli, et al.. (1990). Mapping of chromosome 17 breakpoints in acute myeloid leukemias.. PubMed. 5(10). 1557–63. 29 indexed citations

16.

Longo, Letizia, P P Pandolfi, Andrea Biondi, et al.. (1990). Rearrangements and aberrant expression of the retinoic acid receptor alpha gene in acute promyelocytic leukemias.. The Journal of Experimental Medicine. 172(6). 1571–1575. 156 indexed citations

17.

Donti, Emilio, Letizia Longo, Amedea Mencarelli, et al.. (1989). The Myeloperoxidase Gene in Acute Promyelocytic Leukemia. Science. 244(4906). 824–825. 8 indexed citations

18.

Longo, Letizia, et al.. (1988). N-myc amplification at chromosome band 1p32 in neuroblastoma cells as investigated by in situ hybridization. Journal of Cancer Research and Clinical Oncology. 114(6). 636–640. 35 indexed citations

19.

Donti, Emilio, et al.. (1988). Cytogenetic and molecular study of two human neuroblastoma cell lines. Cancer Genetics and Cytogenetics. 30(2). 225–231. 34 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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