Marta Menéndez

493 total citations
11 papers, 388 citations indexed

About

Marta Menéndez is a scholar working on Molecular Biology, Surgery and Oncology. According to data from OpenAlex, Marta Menéndez has authored 11 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Surgery and 2 papers in Oncology. Recurrent topics in Marta Menéndez's work include RNA modifications and cancer (2 papers), Genetic Syndromes and Imprinting (2 papers) and Head and Neck Anomalies (2 papers). Marta Menéndez is often cited by papers focused on RNA modifications and cancer (2 papers), Genetic Syndromes and Imprinting (2 papers) and Head and Neck Anomalies (2 papers). Marta Menéndez collaborates with scholars based in Spain. Marta Menéndez's co-authors include Eliécer Coto, Marı́a Victoria González, Carlos López‐Larrea, Carlos Suárez, Victoria Álvarez, Raúl F. Pérez, Luı́s Rodrigo, S Aguado, Manuel Fresno and María José Ariza and has published in prestigious journals such as Cancer Research, Critical Care and Journal of Clinical Pathology.

In The Last Decade

Marta Menéndez

11 papers receiving 382 citations

Peers

Marta Menéndez

SURGE

ONCOL

GENET

Nebojša Jović Serbia

Guo-Pei Yu United States

Rosy Mondal India

Ruchira Fernando Australia

Chung‐Ho Chen Taiwan

Giampiero Candeloro Italy

Olçay Kandemir Türkiye

Toshiaki Kamano Japan

Kinichi Yokota Japan

Nebojša Jović Serbia

Marta Menéndez

209 ×0.8

57 ×0.5

SURGE

73 ×0.8

ONCOL

41 ×0.5

GENET

75 ×1.3

Citations per year, relative to Marta Menéndez Marta Menéndez (= 1×) peers Nebojša Jović

Countries citing papers authored by Marta Menéndez

Since Specialization

Citations

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

Fields of papers citing papers by Marta Menéndez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Menéndez

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

All Works

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11 of 11 papers shown

Llorente, José Luís, et al.. (2019). Management of Differentiated Thyroid Carcinomas. Acta Otorrinolaringologica (English Edition). 70(4). 200–206. 1 indexed citations

Menéndez, Marta, Blanca Vivanco, Laura Suárez–Fernández, et al.. (2019). Abstract 3325: EGFR mutation and protein expression analysis in sinonasal inverted papilloma and squamous cell carcinoma. Cancer Research. 79(13_Supplement). 3325–3325. 1 indexed citations

Llorente, José Luís, et al.. (2018). Manejo de los carcinomas diferenciados de tiroides. Acta Otorrinolaringológica Española. 70(4). 200–206. 1 indexed citations

Arnalich, Francisco, Marta Menéndez, Veronica I. Lagos, et al.. (2010). Prognostic value of cell-free plasma DNA in patients with cardiac arrest outside the hospital: an observational cohort study. Critical Care. 14(2). R47–R47. 31 indexed citations

González, Marı́a Victoria, et al.. (1998). Genetic polymorphism of N-acetyltransferase-2, glutathione S-transferase-M1, and cytochromes P450IIE1 and P450IID6 in the susceptibility to head and neck cancer.. Journal of Clinical Pathology. 51(4). 294–298. 83 indexed citations

González, Marı́a Victoria, et al.. (1997). Deletion and methylation of the tumour suppressor gene p16/CDKN2 in primary head and neck squamous cell carcinoma.. Journal of Clinical Pathology. 50(6). 509–512. 48 indexed citations

González, Marı́a Victoria, Luı́s Rodrigo, Carlos López‐Larrea, et al.. (1997). Mutation analysis of the p53, APC, and p16 genes in the Barrett's oesophagus, dysplasia, and adenocarcinoma.. Journal of Clinical Pathology. 50(3). 212–217. 94 indexed citations

Ariza, María José, Victoria Álvarez, Raquel Marín, et al.. (1997). A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes.. Journal of Medical Genetics. 34(7). 587–589. 43 indexed citations

González, Marı́a Victoria, et al.. (1995). Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.. PubMed. 1(9). 1043–9. 58 indexed citations

10.

Coto, Eliécer, S. Castro, S Aguado, et al.. (1995). DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease.. Journal of Medical Genetics. 32(6). 442–445. 24 indexed citations

11.

Coto, Eliécer, et al.. (1994). [Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].. PubMed. 103(18). 681–3. 4 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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