Yolanda Martín

1.9k total citations
45 papers, 940 citations indexed

About

Yolanda Martín is a scholar working on Neurology, Surgery and Epidemiology. According to data from OpenAlex, Yolanda Martín has authored 45 papers receiving a total of 940 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 11 papers in Surgery and 11 papers in Epidemiology. Recurrent topics in Yolanda Martín's work include Neurofibromatosis and Schwannoma Cases (7 papers), Congenital Heart Disease Studies (6 papers) and RNA modifications and cancer (4 papers). Yolanda Martín is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (7 papers), Congenital Heart Disease Studies (6 papers) and RNA modifications and cancer (4 papers). Yolanda Martín collaborates with scholars based in Spain, United States and Australia. Yolanda Martín's co-authors include Concepción Hernández-Chico, Francisco Javier Álvarez Rodríguez, Miguel Navarro, Ignacio del Arco, Amanda J. Roberts, Fernando Rodrı́guez de Fonseca, George F. Koob, Julie A. Chowen, María Ángeles Villanúa and M. Rocı́o A. Carrera and has published in prestigious journals such as Blood, PLoS ONE and Clinical Cancer Research.

In The Last Decade

Yolanda Martín

42 papers receiving 906 citations

Peers

Yolanda Martín
J.H.N. Deck Canada
Andrew L. Rankin United States
Shin Kariya Japan
Francis J. Hahn United States
Jeong Eun Shin South Korea
Yasuya Nomura Japan
Philip A. March United States
Bradley J. Katz United States
Isaac Melamed United States
Valentina Mancini Italy
J.H.N. Deck Canada
Yolanda Martín
Citations per year, relative to Yolanda Martín Yolanda Martín (= 1×) peers J.H.N. Deck

Countries citing papers authored by Yolanda Martín

Since Specialization
Citations

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

Fields of papers citing papers by Yolanda Martín

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yolanda Martín

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

All Works

20 of 20 papers shown
1.
Domínguez, José Antonio Ruiz, Blanca Fuentes, Noemí Núñez Enamorado, et al.. (2024). Multicentric Pediatric Stroke Code: Insight to the first years after implementation. European Journal of Paediatric Neurology. 53. 95–103. 1 indexed citations
2.
Martín, Yolanda, et al.. (2024). Mineralizing angiopathy as a rare cause of pediatric stroke: review and report of two cases. Child s Nervous System. 40(11). 3499–3504. 2 indexed citations
3.
Rodríguez, Anna Duat, Juan Luís Becerra, Sandra Bonache, et al.. (2022). Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?. Journal of Medical Genetics. 59(10). 1017–1023. 7 indexed citations
4.
Martín, Yolanda, et al.. (2022). Prognostic value of somatosensory-evoked potentials in the newborn with hypoxic-ischemic encephalopathy after the introduction of therapeutic hypothermia. European Journal of Pediatrics. 181(4). 1609–1618. 4 indexed citations
5.
Prieto, Laura, et al.. (2019). Prenatal diagnosis of pericallosal lipoma: Systematic review. European Journal of Paediatric Neurology. 23(6). 764–782. 4 indexed citations
6.
Pallás‐Alonso, Carmen Rosa, Begoña Loureiro, Javier de la Cruz, et al.. (2018). Spanish survey on follow‐up programmes for children born very preterm. Acta Paediatrica. 108(6). 1042–1048. 6 indexed citations
7.
Martín, Yolanda, et al.. (2015). Functional Analysis of Mutations in Exon 9 of NF1 Reveals the Presence of Several Elements Regulating Splicing. PLoS ONE. 10(10). e0141735–e0141735. 9 indexed citations
8.
9.
López, María Vázquez, et al.. (2014). Periventricular Nodular Heterotopia and Dystonia Due to an ARFGEF2 Mutation. Pediatric Neurology. 51(3). 461–464. 14 indexed citations
10.
Merino, P., et al.. (2013). Congenital fibrosis of the extraocular muscles: magnetic resonance imaging findings and surgical treatment. Strabismus. 21(3). 183–189. 8 indexed citations
11.
Cruz, Pedro M. Rodríguez, et al.. (2013). Acute hemicerebellitis in children: Case report and review of literature. European Journal of Paediatric Neurology. 17(5). 447–453. 9 indexed citations
12.
Velasco, Ana, et al.. (2012). RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas. Neurogenetics. 13(3). 267–274. 13 indexed citations
13.
León-Luis, Juan A. De, Yolanda Martín, Francisco Gámez, et al.. (2011). Comparison of measurements of the transverse diameter and perimeter of the fetal thymus obtained by magnetic resonance and ultrasound imaging. Journal of Magnetic Resonance Imaging. 33(5). 1100–1105. 14 indexed citations
14.
Valero, M. Carmen, Yolanda Martín, Alba Hernández, et al.. (2011). A Highly Sensitive Genetic Protocol to Detect NF1 Mutations. Journal of Molecular Diagnostics. 13(2). 113–122. 82 indexed citations
15.
Alías, Laura, Sara Bernal, Pablo Fuentes‐Prior, et al.. (2008). Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. Human Genetics. 125(1). 29–39. 131 indexed citations
16.
Marín, Carlos, et al.. (2007). MR imaging of isolated right subclavian artery. Pediatric Radiology. 38(2). 216–219. 8 indexed citations
17.
Marín, Carlos, et al.. (2007). MR imaging of isolated left ventricular apical hypoplasia. Pediatric Radiology. 37(7). 703–705. 17 indexed citations
18.
19.
Rodríguez-Ballesteros, Montserrat, Francisco Castillo, Yolanda Martín, et al.. (2003). Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF). Human Mutation. 22(6). 451–456. 155 indexed citations
20.

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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