Paula Coutinho

9.2k total citations · 2 hit papers
87 papers, 4.7k citations indexed

About

Paula Coutinho is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Paula Coutinho has authored 87 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Cellular and Molecular Neuroscience, 50 papers in Molecular Biology and 23 papers in Neurology. Recurrent topics in Paula Coutinho's work include Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (38 papers) and Neurological diseases and metabolism (16 papers). Paula Coutinho is often cited by papers focused on Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (38 papers) and Neurological diseases and metabolism (16 papers). Paula Coutinho collaborates with scholars based in Portugal, France and Canada. Paula Coutinho's co-authors include Jorge Sequeiros, Carolina Silva, Luís Ruano, Cláudia Melo, Isabel Silveira, José Barros, Clara Barbot, Lawrence J. Schut, Patrı́cia Maciel and K. Wessel and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Paula Coutinho

87 papers receiving 4.6k citations

Hit Papers

International Cooperative Ataxia Rating Scale for pharmac... 1997 2026 2006 2016 1997 2014 250 500 750 1000

Peers

Paula Coutinho
Paula Coutinho
Citations per year, relative to Paula Coutinho Paula Coutinho (= 1×) peers Jean Mathieu

Countries citing papers authored by Paula Coutinho

Since Specialization
Citations

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

Fields of papers citing papers by Paula Coutinho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paula Coutinho

This figure shows the co-authorship network connecting the top 25 collaborators of Paula Coutinho. A scholar is included among the top collaborators of Paula Coutinho 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 Paula Coutinho. Paula Coutinho 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.
Brás, José, Isabel Alonso, Clara Barbot, et al.. (2015). Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4. The American Journal of Human Genetics. 96(3). 474–479. 93 indexed citations
2.
Cruz, Vítor Tedim, J Lopez Pais, Luís Ruano, et al.. (2014). Implementation and Outcomes of a Collaborative Multi-Center Network Aimed at Web-Based Cognitive Training – COGWEB Network. JMIR Mental Health. 1(1). e2–e2. 9 indexed citations
3.
Ruano, Luís, Cláudia Melo, Carolina Silva, & Paula Coutinho. (2014). The Global Epidemiology of Hereditary Ataxia and Spastic Paraplegia: A Systematic Review of Prevalence Studies. Neuroepidemiology. 42(3). 174–183. 416 indexed citations breakdown →
4.
Martins, Sandra, Christopher E. Pearson, Paula Coutinho, et al.. (2014). Modifiers of (CAG)n instability in Machado–Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes. Human Genetics. 133(10). 1311–1318. 25 indexed citations
5.
Loureiro, José Leal, Jorge Pinto‐Basto, Ana M. Lopes, et al.. (2012). Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutations. Genetics in Medicine. 14(1). 143–151. 21 indexed citations
6.
Ferreira, Margarida, et al.. (2008). Elevação da lipase e amilase no doente crítico: estudo retrospectivo. Revista Brasileira de Terapia Intensiva. 20(4). 362–369. 3 indexed citations
7.
Dürr, Alexandra, Agnès Camuzat, Chantal Tallaksen, et al.. (2004). Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia. Archives of Neurology. 61(12). 1867–72. 81 indexed citations
8.
Conceição, Isabel, Mamede de Carvalho, Teresinha Evangelista, et al.. (2003). Gelsolin‐related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies. Muscle & Nerve. 28(6). 715–721. 25 indexed citations
9.
Barbot, Clara, Nobutada Tachi, Pascale Bomont, et al.. (2002). Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34. European Journal of Human Genetics. 10. 272–273. 3 indexed citations
10.
Barbot, Clara, Nobutada Tachi, Naoki Kozuka, et al.. (2001). Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity. The American Journal of Human Genetics. 68(2). 501–508. 58 indexed citations
11.
Barbot, Clara, Paula Coutinho, Rui Chorão, et al.. (2001). Recessive Ataxia With Ocular Apraxia. Archives of Neurology. 58(2). 201–201. 68 indexed citations
12.
Coutinho, Paula. (2000). Neurogenetics. Archives of Neurology. 57(1). 59–59. 1 indexed citations
13.
Silveira, Isabel, Isabel Alonso, Laura Guimarães, et al.. (2000). High Germinal Instability of the (CTG)n at the SCA8 Locus of Both Expanded and Normal Alleles. The American Journal of Human Genetics. 66(3). 830–840. 61 indexed citations
14.
Paúl, Constança, et al.. (1999). Living with Machado-Joseph Disease in a Small Rural Community of the Tagus Valley. Public Health Genomics. 2(4). 190–195. 13 indexed citations
15.
Lima, Manuela, et al.. (1997). Prevalence, geographic distribution, and genealogical investigation of Machado-Joseph disease in the Azores (Portugal).. PubMed. 69(3). 383–91. 14 indexed citations
16.
Lima, Manuela, Augusto Abade, Paula Coutinho, & Francine M. Mayer. (1997). Diffusion of a dominant gene: biodemographic study of the families affected by Machado-Joseph disease in the Islands of the Azores (Portugal). 203–210. 3 indexed citations
17.
Trouillas, P, T Takayanagi, Mark Hallett, et al.. (1997). International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. Journal of the Neurological Sciences. 145(2). 205–211. 1010 indexed citations breakdown →
18.
Silva, Carolina, et al.. (1997). Hereditary Ataxias and Spastic Paraplegias: Methodological Aspects of a Prevalence Study in Portugal. Journal of Clinical Epidemiology. 50(12). 1377–1384. 63 indexed citations
19.
Lopes‐Cendes, Íscia, Patrı́cia Maciel, Stephen J. Kish, et al.. (1996). Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and machado‐joseph disease. Annals of Neurology. 40(2). 199–206. 51 indexed citations
20.
Major, E., et al.. (1983). Meptazinol in the treatment of severe post-operative pain: a comparison with morphine.. PubMed. 59 Suppl 1. 35–40. 9 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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