Florencia Neffa

1.3k total citations
8 papers, 34 citations indexed

About

Florencia Neffa is a scholar working on Pathology and Forensic Medicine, Genetics and Oncology. According to data from OpenAlex, Florencia Neffa has authored 8 papers receiving a total of 34 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pathology and Forensic Medicine, 5 papers in Genetics and 4 papers in Oncology. Recurrent topics in Florencia Neffa's work include Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (3 papers) and BRCA gene mutations in cancer (3 papers). Florencia Neffa is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (3 papers) and BRCA gene mutations in cancer (3 papers). Florencia Neffa collaborates with scholars based in Uruguay, Chile and Argentina. Florencia Neffa's co-authors include Edenir Inêz Palmero, Mev Dominguez–Valentin, Francisco López-Köstner, Carlos Vaccaro, Karin Álvarez, Dirce Maria Carraro, Patricia Esperón, Mauro Rossi, Patrícia Ashton‐Prolla and Adriana Della Valle and has published in prestigious journals such as Genes Chromosomes and Cancer, Familial Cancer and Pathology - Research and Practice.

In The Last Decade

Florencia Neffa

6 papers receiving 34 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Florencia Neffa Uruguay	3	30	17	17	11	7	8	34
Miriam Mints Sweden	4	21 0.7×	13 0.8×	15 0.9×	7 0.6×	8 1.1×	4	35
Anna Allavena Italy	3	13 0.4×	16 0.9×	11 0.6×	6 0.5×	6 0.9×	4	34
Carolien M. Kets Netherlands	4	27 0.9×	9 0.5×	19 1.1×	14 1.3×	19 2.7×	4	45
R. Pedersini Italy	3	16 0.5×	25 1.5×	24 1.4×	23 2.1×	3 0.4×	4	42
Margaret Klint United States	4	18 0.6×	23 1.4×	16 0.9×	17 1.5×	4 0.6×	6	39
Adriana Della Valle Uruguay	6	60 2.0×	42 2.5×	37 2.2×	17 1.5×	8 1.1×	16	70
Carole Corsini France	4	21 0.7×	9 0.5×	18 1.1×	10 0.9×	23 3.3×	6	41
Marina Antelo Spain	4	30 1.0×	22 1.3×	13 0.8×	8 0.7×	12 1.7×	6	43
Pablo Kalfayan Argentina	3	15 0.5×	7 0.4×	10 0.6×	5 0.5×	4 0.6×	8	19
Emilie Bouvignies France	3	15 0.5×	13 0.8×	16 0.9×	4 0.4×	13 1.9×	3	30

Countries citing papers authored by Florencia Neffa

Since Specialization

Citations

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

Fields of papers citing papers by Florencia Neffa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florencia Neffa

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

All Works

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8 of 8 papers shown

1.

Esperón, Patricia, Florencia Neffa, Walter Pavicic, et al.. (2024). A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin America. Familial Cancer. 23(4). 507–513.

2.

Neffa, Florencia, et al.. (2023). CYP2D6 Genotyping and the Clinical Impact on Outcomes in Breast Cancer Tamoxifen-Treated Patients. Personalized Medicine. 20(6). 477–483.

3.

Neffa, Florencia, et al.. (2022). Genetic and epigenetic characteristics of patients with colorectal cancer from Uruguay. Pathology - Research and Practice. 241. 154264–154264. 2 indexed citations

4.

Neffa, Florencia, et al.. (2018). Aggressive mutation in a familial adenomatous polyposis syndrome family: when phenotype guides clinical surveillance. Journal of Gastrointestinal Oncology. 9(3). 553–559. 1 indexed citations

5.

López‐Köstner, Francisco, Adriana Della Valle, Carlos Vaccaro, et al.. (2018). Evaluation of MLH1 variants of unclear significance. Genes Chromosomes and Cancer. 57(7). 350–358. 5 indexed citations

6.

Valle, Adriana Della, et al.. (2017). Cáncer de mama y ovario hereditario en Uruguay: resultados del screening para mutaciones en genes de susceptibilidad por secuenciación de nueva generación. 33(2). 40–52. 2 indexed citations

7.

Vaccaro, Carlos, Bernard Rossi, Francisco López-Köstner, et al.. (2016). Lynch syndrome in South America: past, present and future. Familial Cancer. 15(3). 437–445. 3 indexed citations

8.

Dominguez–Valentin, Mev, Mef Nilbert, Patrik Wernhoff, et al.. (2013). Mutation spectrum in South American Lynch syndrome families. Hereditary Cancer in Clinical Practice. 11(1). 18–18. 21 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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