Miguel Tomás‐Vila

883 total citations
11 papers, 166 citations indexed

About

Miguel Tomás‐Vila is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Miguel Tomás‐Vila has authored 11 papers receiving a total of 166 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Neurology and 2 papers in Surgery. Recurrent topics in Miguel Tomás‐Vila's work include Mitochondrial Function and Pathology (3 papers), Neurological diseases and metabolism (2 papers) and Obstructive Sleep Apnea Research (2 papers). Miguel Tomás‐Vila is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Neurological diseases and metabolism (2 papers) and Obstructive Sleep Apnea Research (2 papers). Miguel Tomás‐Vila collaborates with scholars based in Spain and United States. Miguel Tomás‐Vila's co-authors include Núria Roure, María José Jurado, Francesc Sanmartí, Joaquín Téran‐Santos, María Luz Alonso-Álvarez, Milagros Merino-Andreu, David Gozal, Victoria Domínguez-Márquez, Leonardo Landa Rivera and Alfonso Caro‐Llopis and has published in prestigious journals such as International Journal of Molecular Sciences, Neuropathology and Applied Neurobiology and Clinical Chemistry and Laboratory Medicine (CCLM).

In The Last Decade

Miguel Tomás‐Vila

10 papers receiving 164 citations

Peers

Miguel Tomás‐Vila
Eric Libre United States
I. Simon France
Bijal Jain United States
Karen Pysden United Kingdom
Edward Roufail Australia
Miguel Tomás‐Vila
Citations per year, relative to Miguel Tomás‐Vila Miguel Tomás‐Vila (= 1×) peers Sertan Göktaş

Countries citing papers authored by Miguel Tomás‐Vila

Since Specialization
Citations

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

Fields of papers citing papers by Miguel Tomás‐Vila

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Miguel Tomás‐Vila. 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 Miguel Tomás‐Vila. The network helps show where Miguel Tomás‐Vila may publish in the future.

Co-authorship network of co-authors of Miguel Tomás‐Vila

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

All Works

11 of 11 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.
Vílchez, Juan J., Marina Frasquet, Nuria Muelas, et al.. (2022). A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy. Neuropathology and Applied Neurobiology. 48(5). e12817–e12817. 8 indexed citations
3.
Tomás‐Vila, Miguel, Juan J. Vílchez, Inmaculada Azorı́n, et al.. (2021). Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene. Clinical Genetics. 101(2). 233–241. 9 indexed citations
4.
Tomás‐Vila, Miguel, et al.. (2021). Enfermedad de moyamoya: descripción de una serie de casos pediátricos. Revista de Neurología. 73(8). 261–261.
5.
Frasquet, Marina, Juan F. Vázquez‐Costa, Inmaculada Pitarch Castellano, et al.. (2021). Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center. Annals of Clinical and Translational Neurology. 8(9). 1809–1816. 7 indexed citations
6.
Tomás‐Vila, Miguel, et al.. (2019). Síndrome HaNDL en una niña de 12 años. Revista de Neurología. 69(8). 332–332. 1 indexed citations
7.
Rosello, Mónica, et al.. (2018). A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism. International Journal of Endocrinology and Metabolism. In Press(In Press). e67329–e67329. 14 indexed citations
8.
García‐García, Gema, et al.. (2017). The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease. Clinical Chemistry and Laboratory Medicine (CCLM). 56(2). 229–235. 7 indexed citations
9.
Alonso-Álvarez, María Luz, María José Jurado, Milagros Merino-Andreu, et al.. (2012). Documento de consenso del síndrome de apneas-hipopneas durante el sueño en niños (versión completa). 51(1). 23–50. 1 indexed citations
10.
Alonso-Álvarez, María Luz, David Gozal, María José Jurado, et al.. (2011). Documento de consenso del síndrome de apneas-hipopneas durante el sueño en niños (versión completa). Archivos de Bronconeumología. 47. 2–18. 76 indexed citations
11.
Rivera, Leonardo Landa, et al.. (2008). Vigilancia epidemiológica de la transmisión vertical de la enfermedad de Chagas en tres maternidades de la Comunidad Valenciana. Enfermedades Infecciosas y Microbiología Clínica. 26(10). 609–613. 40 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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