Leonora Luna‐Muñoz

405 total citations
8 papers, 36 citations indexed

About

Leonora Luna‐Muñoz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Leonora Luna‐Muñoz has authored 8 papers receiving a total of 36 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Leonora Luna‐Muñoz's work include Hedgehog Signaling Pathway Studies (2 papers), Congenital Anomalies and Fetal Surgery (2 papers) and Congenital limb and hand anomalies (1 paper). Leonora Luna‐Muñoz is often cited by papers focused on Hedgehog Signaling Pathway Studies (2 papers), Congenital Anomalies and Fetal Surgery (2 papers) and Congenital limb and hand anomalies (1 paper). Leonora Luna‐Muñoz collaborates with scholars based in Mexico. Leonora Luna‐Muñoz's co-authors include Osvaldo M. Mutchinick, Jazmín Arteaga‐Vázquez, Irazú Contreras-Yáñez, Alejandra Ramírez‐Venegas, Beatríz Sánchez-Hernández and Justino Regalado-Piñeda and has published in prestigious journals such as Nicotine & Tobacco Research, American Journal of Medical Genetics Part A and Salud Pública de México.

In The Last Decade

Leonora Luna‐Muñoz

8 papers receiving 36 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leonora Luna‐Muñoz Mexico 5 12 11 10 9 8 8 36
Eulalia Turón‐Viñas Spain 6 23 1.9× 15 1.4× 9 0.9× 4 0.4× 3 0.4× 14 75
Saskia Haitjema Netherlands 2 11 0.9× 6 0.5× 8 0.8× 10 1.1× 6 0.8× 4 48
Lindsay Lambie South Africa 5 13 1.1× 4 0.4× 7 0.7× 14 1.6× 12 1.5× 6 37
Hadassa Rodrigues Santos Brazil 3 7 0.6× 13 1.2× 4 0.4× 24 2.7× 5 0.6× 8 62
Anna Ambrosini Italy 4 22 1.8× 6 0.5× 5 0.5× 10 1.1× 2 0.3× 8 55
Anand Vasudevan Australia 3 14 1.2× 5 0.5× 7 0.7× 9 1.0× 5 0.6× 5 36
Marta Pradas-Juni Spain 5 34 2.8× 9 0.8× 6 0.6× 27 3.0× 22 2.8× 7 75
Lamisse Mansour‐Hendili France 5 36 3.0× 13 1.2× 10 1.0× 21 2.3× 4 0.5× 9 64
Julie Firmin France 4 25 2.1× 5 0.5× 6 0.6× 5 0.6× 5 0.6× 7 48
Lyam Vazquez United States 5 18 1.5× 13 1.2× 5 0.5× 6 0.7× 5 41

Countries citing papers authored by Leonora Luna‐Muñoz

Since Specialization
Citations

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

Fields of papers citing papers by Leonora Luna‐Muñoz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leonora Luna‐Muñoz. 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 Leonora Luna‐Muñoz. The network helps show where Leonora Luna‐Muñoz may publish in the future.

Co-authorship network of co-authors of Leonora Luna‐Muñoz

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

All Works

8 of 8 papers shown
1.
Luna‐Muñoz, Leonora, et al.. (2024). Moderate altitude as a risk factor for isolated congenital malformations. Results from a case–control multicenter–multiregional study. Birth Defects Research. 116(7). e2335–e2335. 1 indexed citations
2.
Luna‐Muñoz, Leonora, et al.. (2022). Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population. Revista de investigaci�n Cl�nica. 74(6). 328–339. 2 indexed citations
3.
Contreras-Yáñez, Irazú, et al.. (2022). Telomeres Length Variations in a Rheumatoid Arthritis Patients Cohort at Early Disease Onset and after Follow-Up. Revista de investigaci�n Cl�nica. 74(4). 202–211. 4 indexed citations
4.
Luna‐Muñoz, Leonora, et al.. (2021). Myelomeningocele genotype–phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways. Birth Defects Research. 113(4). 371–381. 5 indexed citations
5.
Luna‐Muñoz, Leonora, et al.. (2019). Isolated postaxial polydactyly: Epidemiologic characteristics from a multicenter birth defects study. American Journal of Medical Genetics Part A. 179(8). 1432–1441. 2 indexed citations
6.
Arteaga‐Vázquez, Jazmín, et al.. (2019). OEIS complex: Prevalence, clinical, and epidemiologic findings in a multicenter Mexican birth defects surveillance program. Birth Defects Research. 111(11). 666–671. 7 indexed citations
7.
Ramírez‐Venegas, Alejandra, Beatríz Sánchez-Hernández, Leonora Luna‐Muñoz, et al.. (2015). Genetic Risk Determinants for Cigarette Smoking Dependence in Mexican Mestizo Families. Nicotine & Tobacco Research. 18(5). 620–625. 11 indexed citations
8.
Arteaga‐Vázquez, Jazmín, Leonora Luna‐Muñoz, & Osvaldo M. Mutchinick. (2012). Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes. Salud Pública de México. 54(6). 579–586. 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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2026