Jorge Sequeiros

9.7k total citations
209 papers, 5.0k citations indexed

About

Jorge Sequeiros is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Jorge Sequeiros has authored 209 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Molecular Biology, 111 papers in Cellular and Molecular Neuroscience and 57 papers in Genetics. Recurrent topics in Jorge Sequeiros's work include Genetic Neurodegenerative Diseases (108 papers), Mitochondrial Function and Pathology (78 papers) and DNA Repair Mechanisms (36 papers). Jorge Sequeiros is often cited by papers focused on Genetic Neurodegenerative Diseases (108 papers), Mitochondrial Function and Pathology (78 papers) and DNA Repair Mechanisms (36 papers). Jorge Sequeiros collaborates with scholars based in Portugal, France and United Kingdom. Jorge Sequeiros's co-authors include Paula Coutinho, Isabel Silveira, Alda Sousa, José Barros, Isabel Alonso, Teresa Coelho, Patrı́cia Maciel, Laura Bannach Jardim, Carolina Lemos and Milena Paneque and has published in prestigious journals such as Nature Medicine, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jorge Sequeiros

204 papers receiving 4.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jorge Sequeiros Portugal 39 3.3k 2.6k 1.1k 1.0k 450 209 5.0k
Jean Mathieu Canada 38 2.8k 0.9× 3.2k 1.2× 1.8k 1.6× 319 0.3× 505 1.1× 142 4.9k
Richard J. Sinke Netherlands 39 2.2k 0.7× 1.2k 0.4× 543 0.5× 1.2k 1.2× 180 0.4× 119 4.4k
Kari Majamaa Finland 41 4.3k 1.3× 775 0.3× 837 0.7× 1.2k 1.1× 415 0.9× 187 6.7k
Paula Coutinho Portugal 31 2.8k 0.8× 3.3k 1.2× 1.6k 1.4× 371 0.4× 928 2.1× 87 4.7k
Katherine D. Mathews United States 38 4.3k 1.3× 1.8k 0.7× 750 0.7× 668 0.6× 133 0.3× 175 5.9k
Nancy S. Wexler United States 30 3.3k 1.0× 3.4k 1.3× 1.8k 1.6× 951 0.9× 189 0.4× 54 5.0k
Martin B. Delatycki Australia 47 3.9k 1.2× 3.4k 1.3× 1.6k 1.4× 1.8k 1.8× 424 0.9× 336 8.7k
David W. Stockton United States 32 3.3k 1.0× 1.3k 0.5× 483 0.4× 1.3k 1.3× 141 0.3× 70 4.9k
Dena Hernández United States 35 2.6k 0.8× 1.1k 0.4× 1.9k 1.7× 1.4k 1.3× 1.0k 2.3× 73 5.4k
E. Schwinger Germany 40 2.7k 0.8× 1.3k 0.5× 1.0k 0.9× 2.0k 1.9× 303 0.7× 210 6.0k

Countries citing papers authored by Jorge Sequeiros

Since Specialization
Citations

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

Fields of papers citing papers by Jorge Sequeiros

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jorge Sequeiros

This figure shows the co-authorship network connecting the top 25 collaborators of Jorge Sequeiros. A scholar is included among the top collaborators of Jorge Sequeiros 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 Jorge Sequeiros. Jorge Sequeiros 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.
Silva, Paulo, et al.. (2025). Medically Actionable Secondary Findings from Whole-Exome Sequencing (WES) Data in a Sample of 3972 Individuals. International Journal of Molecular Sciences. 26(8). 3509–3509.
2.
Damásio, Joana, Sara Costa, Mariana Santos, et al.. (2025). Movement Disorders in Hereditary Cerebellar Ataxia. Movement Disorders Clinical Practice. 12(6). 784–795.
3.
Barbosa, Maria das Graças Vale, Angus Clarke, Alison Metcalfe, et al.. (2025). Communicating Genetic Information in Families with Inherited Late-Onset Neurodegenerative Diseases: A Scoping Review. Health Communication. 40(12). 2651–2673. 2 indexed citations
4.
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
5.
Couto, Daniela, Jorge Sequeiros, Manuela Lima, Liliana Sousa, & Álvaro Mendes. (2024). From stigma to increased social acceptance? Living with Machado-Joseph disease in São Miguel, Azores, Portugal. Journal of Community Genetics. 16(6). 853–859.
6.
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
7.
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
8.
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
9.
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
10.
Santos, Diana, Teresa Coelho, Miguel Alves‐Ferreira, et al.. (2019). C1QA and C1QC modify age‐at‐onset in familial amyloid polyneuropathy patients. Annals of Clinical and Translational Neurology. 6(4). 748–754. 13 indexed citations
11.
Oliveira, Cláudia, et al.. (2018). A repeat-primed PCR assay for pentanucleotide repeat alleles in spinocerebellar ataxia type 37. Journal of Human Genetics. 63(9). 981–987. 7 indexed citations
12.
Ogun, Shamsideen Abayomi, et al.. (2014). Machado–Joseph disease in a Nigerian family: mutational origin and review of the literature. European Journal of Human Genetics. 23(2). 271–273. 8 indexed citations
13.
Leite, Ângela, et al.. (2013). Anxiety and pre-symptomatic testing for neurodegenerative disorders. 3(2). 14–26. 4 indexed citations
14.
Paneque, Milena, Jorge Sequeiros, & Heather Skirton. (2011). Quality Assessment of Genetic Counseling Process in the Context of Presymptomatic Testing for Late-Onset Disorders: A Thematic Analysis of Three Review Articles. Genetic Testing and Molecular Biomarkers. 16(1). 36–45. 13 indexed citations
15.
Almeida, Teresa, Isabel Alonso, Sandra Martins, et al.. (2009). Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10). PLoS ONE. 4(2). e4553–e4553. 39 indexed citations
16.
Ferro, Anabela, M J Castro, Carolina Lemos, et al.. (2008). The C677T Polymorphism in MTHFR Is Not Associated with Migraine in Portugal. Disease Markers. 25(2). 107–113. 21 indexed citations
17.
Costa, Maria do Carmo, Cristina Costa, Ana Paula Silva, et al.. (2005). Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics. 6(4). 209–215. 34 indexed citations
18.
Leite, Ângela, Constança Paúl, & Jorge Sequeiros. (2002). O bem-estar psicológico em indivíduos de risco para doenças neurológicas hereditárias de aparecimento tardio e controlos. Repositório do ISPA (Instituto Superior de Psicologia Aplicada). 3(2). 113–118. 1 indexed citations
19.
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
20.
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

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jean Mathieu Breakdown of academic impact, for papers by Richard J. Sinke Breakdown of academic impact, for papers by Kari Majamaa Breakdown of academic impact, for papers by Paula Coutinho Breakdown of academic impact, for papers by Katherine D. Mathews Breakdown of academic impact, for papers by Nancy S. Wexler Breakdown of academic impact, for papers by Martin B. Delatycki Breakdown of academic impact, for papers by David W. Stockton Breakdown of academic impact, for papers by Dena Hernández Breakdown of academic impact, for papers by E. Schwinger
Rankless by CCL
2026