Jorge Oliveira

1.5k total citations
56 papers, 694 citations indexed

About

Jorge Oliveira is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jorge Oliveira has authored 56 papers receiving a total of 694 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jorge Oliveira's work include Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (9 papers) and RNA modifications and cancer (8 papers). Jorge Oliveira is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (9 papers) and RNA modifications and cancer (8 papers). Jorge Oliveira collaborates with scholars based in Portugal, United Kingdom and Netherlands. Jorge Oliveira's co-authors include Mário Sousa, Rute Pereira, Rosário Santos, Ana Gonçalves, Manuel Melo Pires, Teresinha Evangelista, Ricardo Taipa, Márcia E. Oliveira, Isabel Fineza and Elsa Bronze-da-Rocha and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Jorge Oliveira

51 papers receiving 686 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 Oliveira Portugal 15 436 219 82 76 70 56 694
Duncan B. Johnstone United States 13 450 1.0× 155 0.7× 35 0.4× 64 0.8× 33 0.5× 16 844
Mélissa Beaudoin Canada 13 424 1.0× 122 0.6× 22 0.3× 93 1.2× 84 1.2× 17 650
Jin He China 12 549 1.3× 174 0.8× 50 0.6× 32 0.4× 70 1.0× 52 1.1k
Tuomo Mantere Finland 12 330 0.8× 243 1.1× 27 0.3× 45 0.6× 36 0.5× 22 605
Panayiota Trifillis United States 15 662 1.5× 153 0.7× 20 0.2× 205 2.7× 96 1.4× 34 940
David F. LePage United States 14 674 1.5× 123 0.6× 50 0.6× 95 1.3× 41 0.6× 19 844
Sunnie Wong United States 9 831 1.9× 360 1.6× 18 0.2× 59 0.8× 37 0.5× 14 1.1k
R. Tyler Hillman United States 16 719 1.6× 215 1.0× 51 0.6× 20 0.3× 24 0.3× 53 1.0k
R. Williamson United Kingdom 12 341 0.8× 270 1.2× 99 1.2× 52 0.7× 19 0.3× 27 703
M. E. Robertson United Kingdom 9 457 1.0× 206 0.9× 58 0.7× 37 0.5× 43 0.6× 13 712

Countries citing papers authored by Jorge Oliveira

Since Specialization
Citations

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

Fields of papers citing papers by Jorge Oliveira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jorge Oliveira

This figure shows the co-authorship network connecting the top 25 collaborators of Jorge Oliveira. A scholar is included among the top collaborators of Jorge Oliveira 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 Oliveira. Jorge Oliveira 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.
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.
3.
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
4.
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
5.
Nogueira, Célia, et al.. (2023). Diagnosis across a cohort of “atypical” atypical and complex parkinsonism. Parkinsonism & Related Disorders. 111. 105408–105408. 1 indexed citations
6.
7.
Oliveira, Jorge, et al.. (2023). Lower Facial Dystonia: An Unexpected Presentation Associated with Pathogenic RFC1 Repeat Expansions. Movement Disorders Clinical Practice. 10(7). 1150–1151. 1 indexed citations
8.
Rodrigues, Esmeralda, et al.. (2022). Congenital heart defects associated with pathogenic variants in WAC gene: Expanding the phenotypic and genotypic spectrum of DeSanto–Shinawi syndrome. American Journal of Medical Genetics Part A. 188(4). 1311–1316.
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.
Moráis, Sara, Jorge Oliveira, Catarina Monteiro, et al.. (2020). αIIbβ3 variants in ten families with autosomal dominant macrothrombocytopenia: Expanding the mutational and clinical spectrum. PLoS ONE. 15(12). e0235136–e0235136. 9 indexed citations
11.
Pereira, Rute, Jorge Oliveira, & Mário Sousa. (2020). Bioinformatics and Computational Tools for Next-Generation Sequencing Analysis in Clinical Genetics. Journal of Clinical Medicine. 9(1). 132–132. 140 indexed citations
12.
Pereira, Rute, Telma Barbosa, Ângela Alves, et al.. (2019). Unveiling the genetic etiology of primary ciliary dyskinesia: When standard genetic approach is not enough. Advances in Medical Sciences. 65(1). 1–11. 5 indexed citations
13.
Pereira, Rute, Jorge Oliveira, Ângela Alves, et al.. (2018). Structural and molecular analysis of the cancer prostate cell line PC3: Oocyte zona pellucida glycoproteins. Tissue and Cell. 55. 91–106. 11 indexed citations
14.
Oliveira, Jorge, Ana Gonçalves, Ricardo Taipa, et al.. (2016). New massive parallel sequencing approach improves the genetic characterization of congenital myopathies. Journal of Human Genetics. 61(6). 497–505. 14 indexed citations
15.
Duarte, Sofia, Sandra Jacinto, Jorge Oliveira, et al.. (2014). Atypical phenotype in two patients with LAMA2 mutations. Neuromuscular Disorders. 24(5). 419–424. 29 indexed citations
16.
Lopes, Pedro, et al.. (2013). Variobox: Automatic Detection and Annotation of Human Genetic Variants. Human Mutation. 35(2). 202–207. 5 indexed citations
17.
Duarte, Sofia, et al.. (2011). Dominant and recessive RYR1 mutations in adults with core lesions and mild muscle symptoms. Muscle & Nerve. 44(1). 102–108. 27 indexed citations
18.
Oliveira, Jorge, et al.. (2011). New Approaches in Molecular Diagnosis and Population Carrier Screening for Spinal Muscular Atrophy. Genetic Testing and Molecular Biomarkers. 15(5). 319–326. 4 indexed citations
19.
Oliveira, Jorge, Cristina Dias, E. Redeker, et al.. (2010). Development of NIPBL Locus-Specific Database Using LOVD: From Novel Mutations to Further Genotype-Phenotype Correlations in Cornelia de Lange Syndrome. Human Mutation. 31(11). 1216–1222. 15 indexed citations
20.
Correia, João, et al.. (2007). Abcesso Hepático Piogénico: Casuística de 19 anos. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 14(3). 128–133. 3 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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