José Barros

3.5k total citations
52 papers, 1.8k citations indexed

About

José Barros is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, José Barros has authored 52 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Psychiatry and Mental health and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in José Barros's work include Migraine and Headache Studies (18 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (10 papers). José Barros is often cited by papers focused on Migraine and Headache Studies (18 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (10 papers). José Barros collaborates with scholars based in Portugal, France and Netherlands. José Barros's co-authors include Jorge Sequeiros, Félix Neto, Alda Sousa, Paula Coutinho, Teresa Coelho, Clara Barbot, Isabel Alonso, José Pereira‐Monteiro, Pedro Mendonça and Carolina Lemos and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

José Barros

49 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José Barros Portugal 22 909 570 398 238 206 52 1.8k
Laurel Morris United Kingdom 30 440 0.5× 334 0.6× 272 0.7× 166 0.7× 167 0.8× 72 2.5k
Gerry Evers‐Kiebooms Belgium 37 629 0.7× 949 1.7× 188 0.5× 73 0.3× 438 2.1× 99 3.3k
Gary W. Beecham United States 24 994 1.1× 418 0.7× 181 0.5× 138 0.6× 581 2.8× 89 2.5k
Donald C. Shields United States 27 441 0.5× 513 0.9× 77 0.2× 108 0.5× 413 2.0× 80 1.9k
Jane A. Cox United States 25 710 0.8× 557 1.0× 136 0.3× 172 0.7× 66 0.3× 52 2.2k
Yota Fujimura Japan 22 497 0.5× 449 0.8× 227 0.6× 54 0.2× 120 0.6× 62 2.0k
Jing Lan China 19 440 0.5× 642 1.1× 115 0.3× 189 0.8× 127 0.6× 41 2.3k
Manuel Mattheisen Germany 30 852 0.9× 241 0.4× 552 1.4× 121 0.5× 59 0.3× 94 2.8k
Christopher Salvatore United States 25 609 0.7× 856 1.5× 1.1k 2.8× 149 0.6× 34 0.2× 66 2.5k
Brigitte Chamak France 21 383 0.4× 629 1.1× 284 0.7× 43 0.2× 89 0.4× 86 2.0k

Countries citing papers authored by José Barros

Since Specialization
Citations

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

Fields of papers citing papers by José Barros

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of José Barros

This figure shows the co-authorship network connecting the top 25 collaborators of José Barros. A scholar is included among the top collaborators of José Barros 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 José Barros. José Barros 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.
Damásio, Joana, Sara Costa, Mariana Santos, et al.. (2025). Movement Disorders in Hereditary Cerebellar Ataxia. Movement Disorders Clinical Practice. 12(6). 784–795.
2.
Oliveira, Jorge, Mariana Santos, Sara Costa, et al.. (2024). Spinocerebellar Ataxias: Phenotypic Spectrum of PolyQ versus Non-Repeat Expansion Forms. The Cerebellum. 23(6). 2258–2268. 1 indexed citations
3.
Oliveira, Jorge, et al.. (2023). Pseudodominance in Friedreich Ataxia—Impact of High Prevalence of Carriers and Intrafamilial Clinical Variation. Movement Disorders Clinical Practice. 10(4). 670–676. 1 indexed citations
4.
Santos, Mariana, Joana Damásio, Susana Carmona, et al.. (2022). Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia. Cells. 11(6). 981–981. 5 indexed citations
5.
Damásio, Joana, Diana Santos, Sara Morais, et al.. (2021). Congenital ataxia due to novel variant in ATP8A2 . Clinical Genetics. 100(1). 79–83. 6 indexed citations
6.
Damásio, Joana, Mariana Santos, Raquel Samões, et al.. (2021). Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clinical Genetics. 100(6). 743–747. 5 indexed citations
7.
Damásio, Joana, et al.. (2021). Rare occurrence of severe blindness and deafness in Friedreich ataxia: a case report. SHILAP Revista de lepidopterología. 8(1). 17–17. 3 indexed citations
8.
Pereira‐Monteiro, José, José Barros, Jorge Sequeiros, et al.. (2013). Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility. PLoS ONE. 8(9). e74087–e74087. 18 indexed citations
9.
Lemos, Carolina, Isabel Alonso, José Barros, et al.. (2012). Assessing Risk Factors for Migraine: Differences in Gender Transmission. PLoS ONE. 7(11). e50626–e50626. 19 indexed citations
10.
Barros, José, Joana Damásio, Assunção Tuna, & José Pereira‐Monteiro. (2012). Migraine-Induced Epistaxis and Sporadic Hemiplegic Migraine: Unusual Features in the Same Patient. Case Reports in Neurology. 4(2). 116–119. 7 indexed citations
11.
Lemos, Carolina, José Pereira‐Monteiro, Denisa Mendonça, et al.. (2010). A role for endothelin receptor type A in migraine without aura susceptibility? A study in Portuguese patients. European Journal of Neurology. 18(4). 649–655. 12 indexed citations
12.
Castro, M J, Anine H Stam, Carolina Lemos, et al.. (2007). Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine. Journal of Human Genetics. 52(12). 990–998. 17 indexed citations
13.
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
14.
Barros, José, et al.. (2006). Enxaqueca: Fisiopatogenia, clínica e tratamento. SHILAP Revista de lepidopterología. 22(4). 2 indexed citations
15.
Costa, Maria do Carmo, Andreia Teixeira‐Castro, Marco Constante, et al.. (2006). Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype. Journal of Human Genetics. 51(8). 645–651. 23 indexed citations
16.
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
17.
Barbot, Clara, Paula Coutinho, Rui Chorão, et al.. (2001). Recessive Ataxia With Ocular Apraxia. Archives of Neurology. 58(2). 201–201. 68 indexed citations
18.
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
19.
Coutinho, Paula, José Barros, Cristina Alves, et al.. (1999). Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias. Archives of Neurology. 56(8). 943–943. 56 indexed citations
20.
Barros, José, et al.. (1994). Epilepsy and Cerebrovascular Diseases in an Outpatient Clinic. Cerebrovascular Diseases. 4(2). 96–100. 14 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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