Susana Teijeira

1.2k total citations
38 papers, 689 citations indexed

About

Susana Teijeira is a scholar working on Molecular Biology, Rheumatology and Physiology. According to data from OpenAlex, Susana Teijeira has authored 38 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Rheumatology and 13 papers in Physiology. Recurrent topics in Susana Teijeira's work include Glycogen Storage Diseases and Myoclonus (14 papers), Lysosomal Storage Disorders Research (12 papers) and Muscle Physiology and Disorders (7 papers). Susana Teijeira is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (14 papers), Lysosomal Storage Disorders Research (12 papers) and Muscle Physiology and Disorders (7 papers). Susana Teijeira collaborates with scholars based in Spain, United States and France. Susana Teijeira's co-authors include Carmen Navarro, José M. Fernández, Beatriz San Millán, Irene Viéitez, Antoni L. Andreu, Carlos Rubio-Terrés, Giuseppe Legname, Miguel A. Martı́n, Stanley B. Prusiner and Mariana N. Dimitrova and has published in prestigious journals such as Brain, Annals of Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Susana Teijeira

37 papers receiving 673 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susana Teijeira Spain 16 322 305 192 120 113 38 689
Irene Viéitez Spain 12 191 0.6× 171 0.6× 134 0.7× 67 0.6× 88 0.8× 21 418
Ali‐Reza Moslemi Sweden 20 162 0.5× 956 3.1× 69 0.4× 154 1.3× 132 1.2× 40 1.2k
F. A. Beemer Netherlands 12 248 0.8× 232 0.8× 293 1.5× 31 0.3× 167 1.5× 21 714
Takekazu Ohi Japan 12 59 0.2× 187 0.6× 55 0.3× 71 0.6× 32 0.3× 27 466
James D. Weisfeld‐Adams United States 14 286 0.9× 284 0.9× 61 0.3× 39 0.3× 90 0.8× 27 663
Elena Procopio Italy 16 53 0.2× 407 1.3× 165 0.9× 60 0.5× 88 0.8× 47 670
Roberto Della Casa Italy 16 311 1.0× 138 0.5× 139 0.7× 33 0.3× 166 1.5× 34 536
Miriam Rigoldi Italy 16 228 0.7× 119 0.4× 286 1.5× 21 0.2× 83 0.7× 29 544
Charalampos Karadimas Greece 14 55 0.2× 473 1.6× 41 0.2× 101 0.8× 135 1.2× 17 627
Christine Broissand France 7 66 0.2× 138 0.5× 175 0.9× 14 0.1× 130 1.2× 10 416

Countries citing papers authored by Susana Teijeira

Since Specialization
Citations

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

Fields of papers citing papers by Susana Teijeira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susana Teijeira

This figure shows the co-authorship network connecting the top 25 collaborators of Susana Teijeira. A scholar is included among the top collaborators of Susana Teijeira 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 Susana Teijeira. Susana Teijeira 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.
Millán, Beatriz San, Carmen Navarro, Julián Fernández-Martín, et al.. (2023). Morphological Hallmarks of Classical Fabry Disease: An Ultrastructural Study in a Large Spanish Family. Journal of Clinical Medicine. 12(17). 5689–5689. 1 indexed citations
2.
Eraña, Hasier, Beatriz San Millán, Jorge M. Charco, et al.. (2022). Description of the first Spanish case of Gerstmann–Sträussler–Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization. Journal of Neurology. 269(8). 4253–4263. 1 indexed citations
3.
Biferi, Maria Grazia, Mathilde Cohen-Tannoudji, Irene Viéitez, et al.. (2020). Systemic Treatment of Fabry Disease Using a Novel AAV9 Vector Expressing α-Galactosidase A. Molecular Therapy — Methods & Clinical Development. 20. 1–17. 20 indexed citations
4.
González, Juan Carlos Montejo, et al.. (2019). Muscle weakness: Understanding the principles of myopathy and neuropathy in the critically ill patient and the management options. Clinical Nutrition. 39(5). 1331–1344. 12 indexed citations
5.
Millán, Beatriz San, Alberto Blázquez, Aitor Delmiro, et al.. (2016). Variable skeletal muscle involvement in VARS2 mitochondrial encephalomyopathy. Neuromuscular Disorders. 26. S178–S178. 1 indexed citations
6.
Lucía, Alejandro, Jonatan R. Ruiz, Alfredo Santalla, et al.. (2012). Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry. Journal of Neurology Neurosurgery & Psychiatry. 83(3). 322–328. 96 indexed citations
7.
Viéitez, Irene, Susana Teijeira, José M. Fernández, et al.. (2011). Molecular and clinical study of McArdle’s disease in a cohort of 123 European patients. Identification of 20 novel mutations. Neuromuscular Disorders. 21(12). 817–823. 28 indexed citations
8.
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
9.
Llano, Luis Pérez de, et al.. (2010). Shrinking lung syndrome caused by lupus myopathy. QJM. 104(3). 259–262. 11 indexed citations
10.
Viéitez, Irene, et al.. (2009). Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.. PubMed. 125(1). 114–335. 6 indexed citations
11.
Nadaj‐Pakleza, Aleksandra, Pascal Laforêt, B. Eymard, et al.. (2009). Permanent muscle weakness in MCArdle disease. Muscle & Nerve. 40(3). 350–357. 46 indexed citations
12.
Navarro, Carmen, Susana Teijeira, & Beatriz San Millán. (2009). Pathology and Diagnosis of Muscular Dystrophies. Advances in experimental medicine and biology. 652. 1–11. 1 indexed citations
13.
Millán, Beatriz San, et al.. (2007). Acute Necrotizing Encephalopathy of Childhood: Report of a Spanish Case. Pediatric Neurology. 37(6). 438–441. 24 indexed citations
14.
Navarro, Carmen, Susana Teijeira, Carmen Domı́nguez, et al.. (2006). Fabry disease: an ultrastructural comparative study of skin in hemizygous and heterozygous patients. Acta Neuropathologica. 111(2). 178–185. 23 indexed citations
15.
Requena, Jesús R., Mariana N. Dimitrova, Giuseppe Legname, et al.. (2004). Oxidation of methionine residues in the prion protein by hydrogen peroxide. Archives of Biochemistry and Biophysics. 432(2). 188–195. 70 indexed citations
16.
Navarro, Cláudia Maria & Susana Teijeira. (2003). Neuromuscular disorders in the Gypsy ethnic group. A short review.. PubMed. 22(1). 11–4. 6 indexed citations
17.
Rivas, Eloy, et al.. (2003). [A brain tissue bank in a neuropathology laboratory. Basic methodology].. PubMed. 18(10). 709–15.
18.
Calvo, Francisco, et al.. (2000). Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients. Neuromuscular Disorders. 10(8). 560–566. 30 indexed citations
19.
Fernández, Roberto, José M. Fernández, Carlos Cervera, et al.. (1999). Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle. Neuromuscular Disorders. 9(3). 136–143. 23 indexed citations
20.
Teijeira, Susana, et al.. (1998). Subsarcolemmal expression of utrophin in neuromuscular disorders: an immunohistochemical study of 80 cases. Acta Neuropathologica. 96(5). 481–486. 7 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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