Pedro Mendonça

1.7k total citations
13 papers, 677 citations indexed

About

Pedro Mendonça is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Pedro Mendonça has authored 13 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Pedro Mendonça's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (5 papers) and DNA Repair Mechanisms (4 papers). Pedro Mendonça is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (5 papers) and DNA Repair Mechanisms (4 papers). Pedro Mendonça collaborates with scholars based in Portugal, Brazil and France. Pedro Mendonça's co-authors include Jorge Sequeiros, Paula Coutinho, José Barros, Clara Barbot, Nobutada Tachi, Naoki Kozuka, Michel Kœnig, Eiji Uchida, Masao Watanabe and Tetsuya Nagata and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Neurology.

In The Last Decade

Pedro Mendonça

11 papers receiving 664 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pedro Mendonça Portugal 10 580 389 102 71 59 13 677
Kevin A. Glenn United States 10 280 0.5× 72 0.2× 56 0.5× 71 1.0× 45 0.8× 18 458
Sophie Aubert France 9 625 1.1× 143 0.4× 34 0.3× 55 0.8× 73 1.2× 14 721
Paolo Marchi United Kingdom 10 223 0.4× 102 0.3× 29 0.3× 42 0.6× 27 0.5× 15 333
Jenna Nguyen United States 5 359 0.6× 156 0.4× 6 0.1× 85 1.2× 49 0.8× 7 468
Ahrin Koppel United States 7 338 0.6× 392 1.0× 215 2.1× 20 0.3× 26 0.4× 9 514
Yumiko Taguchi Japan 9 254 0.4× 82 0.2× 220 2.2× 20 0.3× 31 0.5× 20 595
Kenji Ohtawa Japan 9 373 0.6× 131 0.3× 30 0.3× 50 0.7× 72 1.2× 9 557
Pui Pik Law United Kingdom 8 275 0.5× 130 0.3× 40 0.4× 53 0.7× 27 0.5× 10 383
Mark Moffat United States 11 259 0.4× 112 0.3× 36 0.4× 109 1.5× 38 0.6× 14 402
Ya-Ping Lin United States 10 327 0.6× 79 0.2× 8 0.1× 42 0.6× 31 0.5× 12 458

Countries citing papers authored by Pedro Mendonça

Since Specialization
Citations

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

Fields of papers citing papers by Pedro Mendonça

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pedro Mendonça

This figure shows the co-authorship network connecting the top 25 collaborators of Pedro Mendonça. A scholar is included among the top collaborators of Pedro Mendonça 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 Pedro Mendonça. Pedro Mendonça is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
2.
Mendonça, Pedro, et al.. (2023). Clinically Expired Platelet Concentrates as a Source of Extracellular Vesicles for Targeted Anti-Cancer Drug Delivery. Pharmaceutics. 15(3). 953–953. 10 indexed citations
3.
Almeida, Henrique, et al.. (2022). Pulsed Electric Fields for Valorization of Platelets with No Therapeutic Value towards a High Biomedical Potential Product—A Proof of Concept. Applied Sciences. 12(12). 5773–5773. 5 indexed citations
4.
Conceição, Cláudia, et al.. (2013). Health professionals moving to… and from Portugal. Health Policy. 114(2-3). 97–108. 31 indexed citations
5.
Mota‐Vieira, Luísa, Paula Pacheco, Rita Cabral, et al.. (2006). Human DNA bank in Sao Miguel Island (Azores): A resource for genetic diversity studies. International Congress Series. 1288. 388–390. 11 indexed citations
6.
Pacheco, Paula, Cláudia C. Branco, Rita Cabral, et al.. (2006). The Y-chromosome in the Azores Islands: Phylogeny and diversity. International Congress Series. 1288. 259–261.
7.
Pacheco, Paula, Cláudia C. Branco, Rita Cabral, et al.. (2005). The Y‐chromosomal Heritage of the Azores Islands Population. Annals of Human Genetics. 69(2). 145–156. 20 indexed citations
8.
Jardim, Laura Bannach, Isabel Silveira, Maria Luiza Saraiva Pereira, et al.. (2003). Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype. Acta Neurologica Scandinavica. 107(3). 211–214. 20 indexed citations
9.
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
10.
Barbot, Clara, Paula Coutinho, Rui Chorão, et al.. (2001). Recessive Ataxia With Ocular Apraxia. Archives of Neurology. 58(2). 201–201. 68 indexed citations
11.
Barbot, Clara, Nobutada Tachi, Naoki Kozuka, et al.. (2001). The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin. Nature Genetics. 29(2). 189–193. 323 indexed citations
12.
Jardim, Laura Bannach, Isabel Silveira, Anabela Ferro, et al.. (2001). A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations. Journal of Neurology. 248(10). 870–876. 70 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

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

Rankless by CCL
2026