Rocío Mena

625 total citations
16 papers, 182 citations indexed

About

Rocío Mena is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Rocío Mena has authored 16 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Nephrology. Recurrent topics in Rocío Mena's work include Genetic and Kidney Cyst Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Rocío Mena is often cited by papers focused on Genetic and Kidney Cyst Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Rocío Mena collaborates with scholars based in Spain, Brazil and France. Rocío Mena's co-authors include Pablo Lapunzina, Julián Nevado, Luís Fernández, Elena Vallespín, Mariluce Riegel, María Ángeles Mori, Elena Mansilla, María Torres, María Palomares‐Bralo and Jair Tenorio and has published in prestigious journals such as International Journal of Molecular Sciences, World Journal of Gastroenterology and Molecular Immunology.

In The Last Decade

Rocío Mena

13 papers receiving 180 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rocío Mena Spain 7 75 65 48 32 27 16 182
Max Kros Netherlands 7 64 0.9× 75 1.2× 27 0.6× 19 0.6× 41 1.5× 10 167
Dinu Antony Kuwait 7 155 2.1× 111 1.7× 81 1.7× 26 0.8× 13 0.5× 12 258
Constance Wells France 7 61 0.8× 49 0.8× 14 0.3× 23 0.7× 20 0.7× 11 124
Jaime Sánchez del Pozo Spain 9 106 1.4× 159 2.4× 12 0.3× 25 0.8× 13 0.5× 27 264
Maria Gnazzo Italy 9 184 2.5× 140 2.2× 32 0.7× 9 0.3× 16 0.6× 26 304
Zeynep H. Coban Akdemir United States 7 49 0.7× 65 1.0× 27 0.6× 17 0.5× 6 0.2× 9 172
Saverio Scianguetta Italy 8 19 0.3× 59 0.9× 28 0.6× 16 0.5× 51 1.9× 16 159
B. Thamm Germany 9 41 0.5× 93 1.4× 37 0.8× 7 0.2× 6 0.2× 13 203
Sophie Delahaye France 7 101 1.3× 139 2.1× 60 1.3× 78 2.4× 21 0.8× 11 363
Karina Meden Sørensen Denmark 7 60 0.8× 107 1.6× 23 0.5× 13 0.4× 13 0.5× 9 185

Countries citing papers authored by Rocío Mena

Since Specialization
Citations

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

Fields of papers citing papers by Rocío Mena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rocío Mena

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

All Works

16 of 16 papers shown
1.
Mena, Rocío, Carmen Rodríguez Jiménez, Ángela del Pozo, et al.. (2023). Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts. International Journal of Molecular Sciences. 24(14). 11429–11429. 4 indexed citations
2.
Peces, R., Rocío Mena, Carolina Blanco, et al.. (2023). A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1. Genes. 14(10). 1878–1878. 3 indexed citations
3.
Peces, R., Rocío Mena, Emilio Cuesta, et al.. (2022). Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes. Genes. 13(3). 394–394.
4.
Parrón, Manuel, Christopher T. Gordon, Fernando Santos‐Simarro, et al.. (2022). Broadening the phenotypic spectrum of EVEN‐PLUS syndrome through identification of HSPA9 pathogenic variants in the original EVE dysplasia family and two sibs with milder facial phenotype. American Journal of Medical Genetics Part A. 188(9). 2819–2824.
5.
6.
Peces, R., Rocío Mena, Hernando Trujillo, et al.. (2021). Historical and geographical distribution of the founder mutation c.610G>A; p.Ala204Thr in the CLCNKB gene linked to Bartter syndrome type III in Spain. Clinical Kidney Journal. 14(8). 1990–1993.
7.
Santos‐Simarro, Fernando, Anna M. Cueto‐González, Elena Mansilla, et al.. (2021). Mosaic Variegated Aneuploidy syndrome 2 caused by biallelic variants in CEP57, two new cases and review of the phenotype. European Journal of Medical Genetics. 64(11). 104338–104338. 7 indexed citations
8.
Peces, R., Rocío Mena, Emilio Cuesta, et al.. (2020). Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early‐onset and fast cyst progression. Clinical Genetics. 97(6). 857–868. 3 indexed citations
9.
Peces, R., Rocío Mena, Yolanda Martín, et al.. (2020). Co‐occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2. Molecular Genetics & Genomic Medicine. 8(8). e1321–e1321. 2 indexed citations
10.
Madejón, Antonio, Míriam Romero, Antonio Olveira, et al.. (2019). Prevalence of hepatocarcinoma-related hepatitis B virus mutants in patients in grey zone of treatment. World Journal of Gastroenterology. 25(38). 5883–5896. 9 indexed citations
11.
Peces, R., Rocío Mena, Fernando Santos‐Simarro, et al.. (2019). Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report. Molecular Genetics & Genomic Medicine. 7(4). e00568–e00568. 8 indexed citations
12.
Santos‐Simarro, Fernando, Ángel Campos‐Barros, C. Camarena, et al.. (2017). A new variant in PHKA2 is associated with glycogen storage disease type IXa. Molecular Genetics and Metabolism Reports. 10. 52–55. 16 indexed citations
13.
Tenorio, Jair, Elvira Barrios, Luís Fernández, et al.. (2014). A founder EIF2AK4 mutation causes an aggressive form of pulmonary arterial hypertension in Iberian Gypsies. Clinical Genetics. 88(6). 579–583. 46 indexed citations
14.
Nevado, Julián, María Palomares‐Bralo, Elena Vallespín, et al.. (2014). New microdeletion and microduplication syndromes: a comprehensive review. Genetics and Molecular Biology. 37(1 suppl 1). 210–219. 65 indexed citations
15.
Mena, Rocío, Alberto López‐Lera, & Margarita López‐Trascasa. (2011). Analysis of SERPING1 expression on hereditary angioedema patients: Quantitative analysis of full-length and exon 3 splicing variants. Immunology Letters. 141(2). 158–164. 5 indexed citations
16.
López‐Lera, Alberto, Sofía Garrido, Rocío Mena, Gumersindo Fontán, & Margarita López‐Trascasa. (2009). Molecular characterization of three new mutations causing C5 deficiency in two non-related families. Molecular Immunology. 46(11-12). 2340–2347. 12 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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