Dolores Martínez‐Rubio

825 total citations
23 papers, 555 citations indexed

About

Dolores Martínez‐Rubio is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Dolores Martínez‐Rubio has authored 23 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Dolores Martínez‐Rubio's work include Hereditary Neurological Disorders (12 papers), Genetic Neurodegenerative Diseases (9 papers) and Neurological diseases and metabolism (6 papers). Dolores Martínez‐Rubio is often cited by papers focused on Hereditary Neurological Disorders (12 papers), Genetic Neurodegenerative Diseases (9 papers) and Neurological diseases and metabolism (6 papers). Dolores Martínez‐Rubio collaborates with scholars based in Spain, Czechia and Israel. Dolores Martínez‐Rubio's co-authors include Carmen Espinós, Francesc Palau, Teresa Sevilla, Juan J. Vílchez, Rafael Sivera, María José Chumillas, Vincenzo Lupo, Nuria Muelas, Luís Bataller and Juan F. Vázquez‐Costa and has published in prestigious journals such as Brain, Neurology and Scientific Reports.

In The Last Decade

Dolores Martínez‐Rubio

23 papers receiving 549 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dolores Martínez‐Rubio Spain 13 356 215 161 122 77 23 555
Abdelmadjid Hamri France 6 267 0.8× 168 0.8× 139 0.9× 63 0.5× 55 0.7× 9 433
Amelie Pandraud United Kingdom 7 327 0.9× 167 0.8× 126 0.8× 207 1.7× 54 0.7× 7 523
Stefania Magri Italy 13 271 0.8× 296 1.4× 66 0.4× 115 0.9× 54 0.7× 33 477
Gloria M. Palomo United States 8 107 0.3× 300 1.4× 53 0.3× 205 1.7× 78 1.0× 11 537
Paola Saveri Italy 14 433 1.2× 257 1.2× 127 0.8× 174 1.4× 106 1.4× 23 597
Gautam Wali Australia 12 169 0.5× 119 0.6× 77 0.5× 103 0.8× 50 0.6× 30 363
Swati Naphade United States 12 96 0.3× 182 0.8× 53 0.3× 86 0.7× 34 0.4× 19 416
Francesca Maltecca Italy 14 408 1.1× 644 3.0× 77 0.5× 121 1.0× 83 1.1× 25 727
Emanuela Piermarini Italy 11 172 0.5× 219 1.0× 28 0.2× 40 0.3× 80 1.0× 14 340
Laurie Robak United States 7 270 0.8× 266 1.2× 78 0.5× 121 1.0× 47 0.6× 11 583

Countries citing papers authored by Dolores Martínez‐Rubio

Since Specialization
Citations

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

Fields of papers citing papers by Dolores Martínez‐Rubio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dolores Martínez‐Rubio. 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 Dolores Martínez‐Rubio. The network helps show where Dolores Martínez‐Rubio may publish in the future.

Co-authorship network of co-authors of Dolores Martínez‐Rubio

This figure shows the co-authorship network connecting the top 25 collaborators of Dolores Martínez‐Rubio. A scholar is included among the top collaborators of Dolores Martínez‐Rubio 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 Dolores Martínez‐Rubio. Dolores Martínez‐Rubio 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.
Martínez‐Rubio, Dolores, Clara Marco‐Marín, Vincenzo Lupo, et al.. (2023). Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. International Journal of Molecular Sciences. 24(22). 16400–16400. 3 indexed citations
2.
Jesús, Silvia, Fátima Carrillo, Dolores Martínez‐Rubio, et al.. (2021). NR4A2 Mutations Can Cause Intellectual Disability and Language Impairment With Persistent Dystonia-Parkinsonism. Neurology Genetics. 7(1). e543–e543. 12 indexed citations
3.
Andrés-Bordería, Amparo, Dolores Martínez‐Rubio, Luba Blumkin, et al.. (2021). Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration. International Journal of Molecular Sciences. 22(5). 2505–2505. 8 indexed citations
4.
Ruiz, Pedro, Dolores Martínez‐Rubio, Mario Ezquerra, et al.. (2021). Regulatory rare variants of the dopaminergic gene ANKK1 as potential risk factors for Parkinson’s disease. Scientific Reports. 11(1). 9879–9879. 4 indexed citations
5.
Frasquet, Marina, Ricard Rojas‐García, Juan F. Vázquez‐Costa, et al.. (2020). Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation. European Journal of Neurology. 28(4). 1334–1343. 42 indexed citations
6.
Espinós, Carmen, Máximo Ibo Galindo, Maria Adelaida García-Gimeno, et al.. (2020). Oxidative Stress, a Crossroad Between Rare Diseases and Neurodegeneration. Antioxidants. 9(4). 313–313. 48 indexed citations
7.
Frasquet, Marina, Dolores Martínez‐Rubio, Inmaculada Pitarch Castellano, et al.. (2019). A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4. Journal of the Neurological Sciences. 402. 156–161. 6 indexed citations
8.
Lupo, Vincenzo, Marina Frasquet, Ana L. Pelayo‐Negro, et al.. (2018). Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations. Journal of Medical Genetics. 55(12). 814–823. 15 indexed citations
9.
Sevilla, Teresa, Vincenzo Lupo, Dolores Martínez‐Rubio, et al.. (2015). Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease. Brain. 139(1). 62–72. 58 indexed citations
10.
Hoenicka, Janet, Pedro Ruiz, G. Ponce, et al.. (2014). The Addiction-Related Gene ANKK1 in Parkinsonian Patients with Impulse Control Disorder. Neurotoxicity Research. 27(3). 205–208. 16 indexed citations
11.
Calpena, Eduardo, Dolores Martínez‐Rubio, Javier Arpa, et al.. (2014). A novel locus for a hereditary recurrent neuropathy on chromosome 21q21. Neuromuscular Disorders. 24(8). 660–665. 2 indexed citations
12.
Sevilla, Teresa, Dolores Martínez‐Rubio, Catalina Márquez-Vega, et al.. (2012). Genetics of the Charcot‐Marie‐Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy‐Russe in depth. Clinical Genetics. 83(6). 565–570. 25 indexed citations
13.
Calpena, Eduardo, Mercedes Casado, Dolores Martínez‐Rubio, et al.. (2012). 5-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense Changes. JIMD Reports. 7. 123–128. 13 indexed citations
14.
Espinós, Carmen, Eduardo Calpena, Dolores Martínez‐Rubio, & Vincenzo Lupo. (2012). Autosomal Recessive Charcot-Marie-Tooth Neuropathy. Advances in experimental medicine and biology. 724. 61–75. 4 indexed citations
15.
Sevilla, Teresa, Vincenzo Lupo, Rafael Sivera, et al.. (2011). Congenital hypomyelinating neuropathy due to a novel MPZ mutation. Journal of the Peripheral Nervous System. 16(4). 347–352. 12 indexed citations
16.
Pineda, Mercè, Raquel Montero, Ana Mas, et al.. (2010). Coenzyme Q10‐responsive ataxia: 2‐year‐treatment follow‐up. Movement Disorders. 25(9). 1262–1268. 39 indexed citations
17.
Espinós, Carmen, Àngels García‐Cazorla, Dolores Martínez‐Rubio, et al.. (2010). Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuria. Clinical Genetics. 78(6). 554–559. 9 indexed citations
18.
Sivera, Rafael, Carmen Espinós, Juan J. Vílchez, et al.. (2010). Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot‐Marie‐Tooth disease. Journal of the Peripheral Nervous System. 15(4). 334–344. 54 indexed citations
19.
Lupo, Vincenzo, Máximo Ibo Galindo, Dolores Martínez‐Rubio, et al.. (2009). Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway. Human Molecular Genetics. 18(23). 4603–4614. 47 indexed citations
20.
Fernández‐Burriel, Miguel, et al.. (2008). A Novel Delins Mutation in the α-TTP Gene in a Family Segregating Ataxia With Isolated Vitamin E Deficiency. Pediatric Research. 64(3). 262–264. 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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