M.J. Sobrido

614 total citations
19 papers, 370 citations indexed

About

M.J. Sobrido is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, M.J. Sobrido has authored 19 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Neurology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in M.J. Sobrido's work include Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Genomics and Rare Diseases (4 papers). M.J. Sobrido is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Genomics and Rare Diseases (4 papers). M.J. Sobrido collaborates with scholars based in Spain, United States and Austria. M.J. Sobrido's co-authors include Manuel Arias, Daniel H. Geschwind, Adriano Jiménez‐Escrig, Julio Pardo, José Ramón Fernández Lorenzo, J. Duarte, Belén Pilo‐de‐la‐Fuente, María García-Murias, Ãngel Carracedo and Jeremy A. Cholfin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Cancer.

In The Last Decade

M.J. Sobrido

19 papers receiving 365 citations

Peers

M.J. Sobrido

SURGE

CMN

NEURO

ONCOL

Katsuhito Yasuno United States

Alan T. Tang United States

Coro Sánchez‐Quintana Spain

James P. Leu United States

Magda Barsoum‐Homsy Canada

Athina Kladi Greece

Farid Meggouh France

Lindsey D. Goodman United States

Nomingerel Tserentsoodol United States

Andrea Legati Italy

Katsuhito Yasuno United States

M.J. Sobrido

274 ×1.2

55 ×0.5

SURGE

100 ×1.1

CMN

134 ×1.6

NEURO

29 ×0.5

ONCOL

Citations per year, relative to M.J. Sobrido M.J. Sobrido (= 1×) peers Katsuhito Yasuno

Countries citing papers authored by M.J. Sobrido

Since Specialization

Citations

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

Fields of papers citing papers by M.J. Sobrido

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.J. 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 M.J. Sobrido. The network helps show where M.J. Sobrido may publish in the future.

Co-authorship network of co-authors of M.J. Sobrido

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

All Works

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19 of 19 papers shown

Arias, Manuel, Pablo Mir, Marta Fernández‐Matarrubia, et al.. (2021). Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: first families detected in Spain. SHILAP Revista de lepidopterología. 37(4). 257–262. 1 indexed citations

Arias, Manuel, Raquel Cruz, Beatriz Quintáns, et al.. (2020). Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36). The Cerebellum. 19(4). 501–509. 9 indexed citations

Arias, Manuel, Pablo Mir, Marta Fernández‐Matarrubia, et al.. (2019). Heredoataxia cerebelosa recesiva ARCA1/SCAR8: primeras familias detectadas en España. Neurología. 37(4). 257–262. 2 indexed citations

Cacheiro, Pilar, Andrés Ordóñez‐Ugalde, Beatriz Quintáns, et al.. (2017). Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants. Molecular Diagnosis & Therapy. 21(3). 303–313. 6 indexed citations

Arias, Manuel, María García-Murias, & M.J. Sobrido. (2017). Spinocerebellar ataxia 36 (SCA36): “Costa da Morte ataxia”. SHILAP Revista de lepidopterología. 32(6). 386–393. 10 indexed citations

Arias, Manuel, María García-Murias, & M.J. Sobrido. (2015). La ataxia espinocerebelosa 36 (SCA36): «Ataxia da Costa da Morte». Neurología. 32(6). 386–393. 9 indexed citations

Taboada, M., et al.. (2014). Automated semantic annotation of rare disease cases: a case study. Database. 2014(0). bau045–bau045. 24 indexed citations

Calviño, Jesús, María M. Adeva, & M.J. Sobrido. (2012). Membranous nephropathy, leiomyoma and autoimmune myasthenia: more than a coincidence?. Clinical Kidney Journal. 5(6). 562–565. 3 indexed citations

Sobrido, M.J., et al.. (2011). Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis. SHILAP Revista de lepidopterología. 26(7). 397–404. 15 indexed citations

10.

Sobrido, M.J., et al.. (2011). Utilidad de los niveles de colestanol en el diagnóstico y seguimiento de los pacientes con xantomatosis cerebrotendinosa. Neurología. 26(7). 397–404. 11 indexed citations

11.

Pilo‐de‐la‐Fuente, Belén, Adriano Jiménez‐Escrig, José Ramón Fernández Lorenzo, et al.. (2011). Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic survey. European Journal of Neurology. 18(10). 1203–1211. 101 indexed citations

12.

Quintáns, Beatriz, Montse Fernández‐Prieto, Ãngel Carracedo, & M.J. Sobrido. (2010). Asesoramiento genético en Neurología: un problema complejo que necesita regulación. Neurología. 26(3). 129–136. 2 indexed citations

13.

Blanco, Patricia, Anja P. Einholm, Hafsa Mamsa, et al.. (2009). A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism. Human Molecular Genetics. 18(13). 2370–2377. 45 indexed citations

14.

Oliveira, João Ricardo Mendes de, M.J. Sobrido, Elizabeth Spiteri, et al.. (2007). Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification (“Fahr” Disease’). Journal of Molecular Neuroscience. 33(2). 151–154. 20 indexed citations

15.

Sobrido, M.J., Sandra Weıntraub, Nancy Johnson, et al.. (2003). Possible association of the tau H1/H1 genotype with primary progressive aphasia. Neurology. 60(5). 862–864. 32 indexed citations

16.

Sobrido, M.J., Jeremy A. Cholfin, Susan Perlman, Stefan M. Pulst, & Daniel H. Geschwind. (2001). SCA8 repeat expansions in ataxia: A controversial association. Neurology. 57(7). 1310–1312. 37 indexed citations

17.

Vega, Ana, M.J. Sobrido, Clara Ruíz-Ponte, Francisco Barros, & Ãngel Carracedo. (2001). RareHRAS1 alleles are a risk factor for the development of brain tumors. Cancer. 92(11). 2920–2926. 10 indexed citations

18.

Peñaranda, José Manuel Suárez, et al.. (2001). Analysis of 2 Antiapoptotic Factors in Gliomas. Archives of Pathology & Laboratory Medicine. 125(2). 218–223. 14 indexed citations

19.

Sobrido, M.J.. (2000). Low frequency of replication errors in primary nervous system tumours. Journal of Neurology Neurosurgery & Psychiatry. 69(3). 369–375. 19 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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