María‐Jesús Sobrido

918 total citations
30 papers, 563 citations indexed

About

María‐Jesús Sobrido is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, María‐Jesús Sobrido has authored 30 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in María‐Jesús Sobrido's work include Genomics and Rare Diseases (7 papers), Hereditary Neurological Disorders (6 papers) and Migraine and Headache Studies (5 papers). María‐Jesús Sobrido is often cited by papers focused on Genomics and Rare Diseases (7 papers), Hereditary Neurological Disorders (6 papers) and Migraine and Headache Studies (5 papers). María‐Jesús Sobrido collaborates with scholars based in Spain, United States and Netherlands. María‐Jesús Sobrido's co-authors include Beatriz Quintáns, Bru Cormand, Alfons Macaya, Ángel Carracedo, João Ricardo Mendes de Oliveira, Roser Corominas, Jessica Fernández‐Morales, Patricia Blanco, Patricia Pozo‐Rosich and Pilar Cacheiro and has published in prestigious journals such as Brain, Neurology and Journal of the Neurological Sciences.

In The Last Decade

María‐Jesús Sobrido

30 papers receiving 547 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María‐Jesús Sobrido Spain 15 214 102 96 91 88 30 563
Yan Zhan China 13 225 1.1× 81 0.8× 29 0.3× 44 0.5× 179 2.0× 35 710
Ali Sazcı Türkiye 19 255 1.2× 45 0.4× 185 1.9× 168 1.8× 87 1.0× 42 993
Matthew T. Goodus United States 12 123 0.6× 87 0.9× 66 0.7× 27 0.3× 33 0.4× 13 479
Masanori Iwai Japan 17 385 1.8× 305 3.0× 49 0.5× 45 0.5× 98 1.1× 45 1.3k
Wallaya Jongjaroenprasert Thailand 12 327 1.5× 97 1.0× 19 0.2× 71 0.8× 238 2.7× 22 767
Wenli Sheng China 13 200 0.9× 53 0.5× 60 0.6× 42 0.5× 139 1.6× 39 641
Jiasi Li China 12 148 0.7× 37 0.4× 40 0.4× 33 0.4× 55 0.6× 26 513
Emily Fessler United States 9 289 1.4× 75 0.7× 58 0.6× 48 0.5× 44 0.5× 11 581
Brittany L. Adler United States 13 147 0.7× 83 0.8× 43 0.4× 25 0.3× 70 0.8× 31 570
Kenneth C. Dole United States 7 174 0.8× 77 0.8× 124 1.3× 47 0.5× 61 0.7× 7 638

Countries citing papers authored by María‐Jesús Sobrido

Since Specialization
Citations

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

Fields of papers citing papers by María‐Jesús Sobrido

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by María‐Jesús Sobrido. 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 María‐Jesús Sobrido. The network helps show where María‐Jesús Sobrido may publish in the future.

Co-authorship network of co-authors of María‐Jesús Sobrido

This figure shows the co-authorship network connecting the top 25 collaborators of María‐Jesús Sobrido. A scholar is included among the top collaborators of María‐Jesús Sobrido 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 María‐Jesús Sobrido. María‐Jesús Sobrido 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.
Navas‐Sánchez, Francisco J., Daniel Martín de Blas, Yasser Alemán‐Gómez, et al.. (2022). Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study. Journal of Neurology. 269(6). 3189–3203. 3 indexed citations
2.
Quintáns, Beatriz, João Ricardo Mendes de Oliveira, & María‐Jesús Sobrido. (2018). Primary familial brain calcifications. Handbook of clinical neurology. 147. 307–317. 26 indexed citations
3.
Sesar, Ángel, Pilar Cacheiro, Marisol López, et al.. (2016). Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico. Journal of the Neurological Sciences. 362. 321–325. 18 indexed citations
4.
Arias, Manuel, et al.. (2015). Targeted NGS meets expert clinical characterization: Efficient diagnosis of spastic paraplegia type 11. PubMed. 5. 33–36. 4 indexed citations
5.
Quintáns, Beatriz, Andrés Ordóñez‐Ugalde, Pilar Cacheiro, Ángel Carracedo, & María‐Jesús Sobrido. (2014). Medical genomics: The intricate path from genetic variant identification to clinical interpretation. PubMed. 3(3). 60–67. 23 indexed citations
6.
Fachal, Laura, Ana Mosquera‐Miguel, Pau Pástor, et al.. (2014). No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(1). 54–65. 39 indexed citations
7.
Taboada, M., et al.. (2013). SNOMED CT module-driven clinical archetype management. Journal of Biomedical Informatics. 46(3). 388–400. 10 indexed citations
8.
Sintas, Cèlia, Jessica Fernández‐Morales, Pilar Cacheiro, et al.. (2012). A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample. Cephalalgia. 32(14). 1076–1080. 11 indexed citations
9.
Sobrido, María‐Jesús, Pilar Cacheiro, Ángel Carracedo, & Lars Bertram. (2012). Databases for neurogenetics: Introduction, overview, and challenges. Human Mutation. 33(9). 1311–1314. 3 indexed citations
10.
Bettencourt, Conceição, Beatriz Quintáns, Raquel Ros, et al.. (2012). Revisiting genotype-phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias. Human Mutation. 33(9). 1315–1323. 13 indexed citations
11.
Quintáns, Beatriz, José Ruiz Pardo, Berta Campos, et al.. (2011). Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. Case Reports in Neurology. 3(1). 86–90. 12 indexed citations
12.
Seijo‐Martínez, Manuel, et al.. (2011). Prevalence of parkinsonism and Parkinson's disease in the Arosa Island (Spain): A community-based door-to-door survey. Journal of the Neurological Sciences. 304(1-2). 49–54. 15 indexed citations
13.
Ortolano, Saida, Rosa Tarrı́o, Patricia Blanco, et al.. (2011). A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy. Neuromuscular Disorders. 21(4). 254–262. 35 indexed citations
14.
Corominas, Roser, Jessica Fernández‐Morales, María‐Jesús Sobrido, et al.. (2011). SNP variants within the vanilloidTRPV1andTRPV3receptor genes are associated with migraine in the Spanish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(1). 94–103. 66 indexed citations
15.
Povey, Sue, Aida I. Al Aqeel, Anne Cambon‐Thomsen, et al.. (2010). Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs). Human Mutation. 31(11). 1179–1184. 28 indexed citations
16.
Corominas, Roser, María‐Jesús Sobrido, Marta Ribasès, et al.. (2009). Association study of the serotoninergic system in migraine in the spanish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 177–184. 35 indexed citations
17.
Corominas, Roser, Marta Ribasès, Ester Cuenca-León, et al.. (2009). Two-stage case-control association study of dopamine-related genes and migraine. BMC Medical Genetics. 10(1). 95–95. 25 indexed citations
18.
Arias, Manuel, Julio Pardo, Patricia Blanco, et al.. (2006). Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation. Neuromuscular Disorders. 16(8). 498–503. 20 indexed citations
19.
Peñaranda, José Manuel Suárez, et al.. (2000). Value of MIB-1 labelling index (LI) in gliomas and its correlation with other prognostic factors. A clinicopathologic study.. PubMed. 44(4). 203–9; discussion 209. 26 indexed citations
20.
Aldrey, José Manuel, et al.. (1996). [Cerebral hemorrhage and migraine].. PubMed. 24(126). 183–6. 1 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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