Teresa Temudo

1.7k total citations
51 papers, 1.0k citations indexed

About

Teresa Temudo is a scholar working on Genetics, Cognitive Neuroscience and Neurology. According to data from OpenAlex, Teresa Temudo has authored 51 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 15 papers in Cognitive Neuroscience and 13 papers in Neurology. Recurrent topics in Teresa Temudo's work include Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (14 papers) and Botulinum Toxin and Related Neurological Disorders (5 papers). Teresa Temudo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (14 papers) and Botulinum Toxin and Related Neurological Disorders (5 papers). Teresa Temudo collaborates with scholars based in Portugal, United States and Spain. Teresa Temudo's co-authors include Patrı́cia Maciel, José Pedro Vieira, Guiomar Oliveira, Eulália Calado, Jorge Sequeiros, Ana Isabel Dias, Pedro Cabral, M. Pineda, Ana Moreira and Sylvie Goldman and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Epilepsia.

In The Last Decade

Teresa Temudo

46 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Teresa Temudo Portugal 16 413 299 291 263 180 51 1.0k
Deborah K. Sokol United States 19 431 1.0× 303 1.0× 174 0.6× 374 1.4× 125 0.7× 56 1.1k
Edvige Veneselli Italy 17 210 0.5× 190 0.6× 352 1.2× 236 0.9× 306 1.7× 41 1.1k
Josette Mancini France 19 454 1.1× 484 1.6× 224 0.8× 305 1.2× 79 0.4× 29 1.2k
Ryoichi Sakuta Japan 22 408 1.0× 841 2.8× 359 1.2× 256 1.0× 72 0.4× 59 1.7k
Xinhua Bao China 24 864 2.1× 1.1k 3.6× 388 1.3× 341 1.3× 159 0.9× 130 2.0k
Francesca Darra Italy 24 522 1.3× 365 1.2× 819 2.8× 285 1.1× 131 0.7× 86 1.6k
M. Pineda Spain 22 398 1.0× 618 2.1× 299 1.0× 253 1.0× 92 0.5× 51 1.7k
Julie S. Cohen United States 22 578 1.4× 617 2.1× 176 0.6× 76 0.3× 121 0.7× 44 1.4k
Nupur Nag Australia 15 368 0.9× 289 1.0× 66 0.2× 295 1.1× 60 0.3× 50 919
Amirthagowri Ambalavanan Canada 15 348 0.8× 335 1.1× 65 0.2× 77 0.3× 135 0.8× 31 795

Countries citing papers authored by Teresa Temudo

Since Specialization
Citations

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

Fields of papers citing papers by Teresa Temudo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Temudo

This figure shows the co-authorship network connecting the top 25 collaborators of Teresa Temudo. A scholar is included among the top collaborators of Teresa Temudo 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 Teresa Temudo. Teresa Temudo 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.
Martins, Joana, et al.. (2022). Trastornos paroxísticos del movimiento de carácter benigno y transitorio en la infancia. Revista de Neurología. 74(4). 135–135.
2.
Soares, Gabriela, Cecília Silva, Rosário Santos, et al.. (2020). Two Compound Heterozygous Variants in SNX14 Cause Stereotypies and Dystonia in Autosomal Recessive Spinocerebellar Ataxia 20. Frontiers in Genetics. 11. 1038–1038. 3 indexed citations
3.
Martins, Joana, Alejandra Darling, Cristina Garrido, et al.. (2019). Sensory Tricks in Pantothenate Kinase‐Associated Neurodegeneration: Video‐Analysis of 43 Patients. Movement Disorders Clinical Practice. 6(8). 704–707. 1 indexed citations
4.
Melo, Cláudia, et al.. (2016). Idiopathic toe walking in children and adolescents. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 25(1). 27–34. 1 indexed citations
5.
Lopes, Fátima, Mafalda Barbosa, Adam Ameur, et al.. (2016). Identification of novel genetic causes of Rett syndrome-like phenotypes. Journal of Medical Genetics. 53(3). 190–199. 126 indexed citations
6.
Lopes, Fátima, Mafalda Barbosa, Teresa Temudo, et al.. (2015). ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing. International Journal of Developmental Neuroscience. 47(Part_A). 99–99.
7.
Ramalheira, João, et al.. (2014). Resective surgery in the treatment of super-refractory partial status epilepticus secondary to NMDAR antibody encephalitis. European Journal of Paediatric Neurology. 18(3). 449–452. 27 indexed citations
8.
Garrido, Cristina, et al.. (2014). Esclerosis tuberosa: caracterización clínica e intento de correlación fenotipo/genotipo. Anales de Pediatría. 81(5). 289–296. 7 indexed citations
9.
Goldman, Sylvie & Teresa Temudo. (2012). Hand stereotypies distinguish Rett syndrome from autism disorder. Movement Disorders. 27(8). 1060–1062. 20 indexed citations
10.
Sequeiros, Jorge, et al.. (2009). Trastornos nutricionales y gastrointestinales en el síndrome de Rett: importancia de la intervención temprana. Anales de Pediatría. 72(3). 191–198. 10 indexed citations
11.
Pineda, M., Mar O’Callaghan, Marina Vilaseca, et al.. (2009). Clinical experience with miglustat therapy in pediatric patients with Niemann–Pick disease type C: A case series. Molecular Genetics and Metabolism. 99(4). 358–366. 93 indexed citations
12.
Temudo, Teresa, Patrı́cia Maciel, & Jorge Sequeiros. (2007). Abnormal movements in Rett syndrome are present before the regression period: A case study. Movement Disorders. 22(15). 2284–2287. 18 indexed citations
13.
Marini, Carla, Davide Mei, Teresa Temudo, et al.. (2007). Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities. Epilepsia. 48(9). 1678–1685. 132 indexed citations
14.
Ramaekers, V., J.M. Sequeira, Rafael Artuch, et al.. (2007). Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome. Neuropediatrics. 38(4). 179–183. 49 indexed citations
15.
Tavares, Susana M., et al.. (2007). Tics en niños y adolescentes: análisis retrospectivo de 78 casos. Anales de Pediatría. 66(2). 129–134. 12 indexed citations
16.
Vries, Boukje de, Carolina Lemos, Teresa Temudo, et al.. (2007). Two novel functional mutations in the Na+,K+‐ATPase α2‐subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. Clinical Genetics. 73(1). 37–43. 26 indexed citations
17.
Temudo, Teresa. (2004). [Paroxysmal dyskinesias in children].. PubMed. 38(1). 53–7. 1 indexed citations
18.
Temudo, Teresa. (2004). Discinesia paroxística en la infancia. Revista de Neurología. 38(1). 53–53. 1 indexed citations
19.
Pineda, M., Marta Vilaseca, Teresa Temudo, et al.. (1996). Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome.. Archives of Disease in Childhood. 74(3). 242–243. 13 indexed citations
20.
Pineda, Mercè, Jaume Campistol, Marina Vilaseca, et al.. (1995). An atypical French form of pyruvate carboxylase deficiency. Brain and Development. 17(4). 276–279. 15 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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