Tiago Matos

469 total citations
22 papers, 332 citations indexed

About

Tiago Matos is a scholar working on Molecular Biology, Sensory Systems and Spectroscopy. According to data from OpenAlex, Tiago Matos has authored 22 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Sensory Systems and 5 papers in Spectroscopy. Recurrent topics in Tiago Matos's work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Connexins and lens biology (9 papers) and Protein purification and stability (6 papers). Tiago Matos is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (10 papers), Connexins and lens biology (9 papers) and Protein purification and stability (6 papers). Tiago Matos collaborates with scholars based in Portugal, Sweden and United Kingdom. Tiago Matos's co-authors include João A. Queiroz, Leif Bülow, Helena Caria, D.M.F. Prazeres, Fani Sousa, Graça Fialho, O Dias, Mário Andrea, Folke Tjerneld and Juliana Silva da Luz and has published in prestigious journals such as SHILAP Revista de lepidopterología, Analytical Biochemistry and Journal of Chromatography A.

In The Last Decade

Tiago Matos

22 papers receiving 328 citations

Peers

Tiago Matos

RNMI

Jacob P. Keller United States

Mariana C. Fiori United States

Michael David Clark United States

Nicolás Enrique Argentina

Le Xie China

Tina Bugge Pedersen Norway

Sébastien Febvay United States

Byeonghyeon Lee South Korea

Joachim Hermann United States

Jacob P. Keller United States

Tiago Matos

181 ×0.8

81 ×0.8

0 ×0.0

11 ×0.3

RNMI

31 ×0.9

Citations per year, relative to Tiago Matos Tiago Matos (= 1×) peers Jacob P. Keller

Countries citing papers authored by Tiago Matos

Since Specialization

Citations

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

Fields of papers citing papers by Tiago Matos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tiago Matos

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

All Works

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20 of 20 papers shown

Matos, Tiago & Leif Bülow. (2018). Separation of Nucleic Acids Using Single- and Multimodal Chromatography. Current Protein and Peptide Science. 20(1). 49–55. 4 indexed citations

Matos, Tiago, et al.. (2017). Fetal hemoglobin is much less prone to DNA cleavage compared to the adult protein. Redox Biology. 12. 114–120. 23 indexed citations

Matos, Tiago, Elsayed T. Mohamed, João A. Queiroz, & Leif Bülow. (2016). Capto™ Resins for Chromatography of DNA: A Minor Difference in Ligand Composition Greatly Influences the Separation of Guanidyl-Containing Fragments. Chromatographia. 79(19-20). 1277–1282. 2 indexed citations

Matos, Tiago, et al.. (2015). The controversial p.Met34Thr variant in GJB2 gene: Two siblings, one genotype, two phenotypes. International Journal of Pediatric Otorhinolaryngology. 79(8). 1316–1319. 3 indexed citations

Matos, Tiago, et al.. (2015). Preparative isolation of polymerase chain reaction products using mixed-mode chromatography. Analytical Biochemistry. 489. 73–75. 6 indexed citations

Matos, Tiago, et al.. (2014). WFS1 and non-syndromic low-frequency sensorineural hearing loss: A novel mutation in a Portuguese case. Gene. 538(2). 288–291. 13 indexed citations

Matos, Tiago, João A. Queiroz, & Leif Bülow. (2014). Plasmid DNA purification using a multimodal chromatography resin. Journal of Molecular Recognition. 27(4). 184–189. 31 indexed citations

Matos, Tiago, João A. Queiroz, & Leif Bülow. (2013). Binding and elution behavior of small deoxyribonucleic acid fragments on a strong anion-exchanger multimodal chromatography resin. Journal of Chromatography A. 1302. 40–44. 16 indexed citations

Matos, Tiago, Silja Senkbeil, António Mendonça, et al.. (2013). Nucleic acid and protein extraction from electropermeabilized E. coli cells on a microfluidic chip. The Analyst. 138(24). 7347–7347. 5 indexed citations

10.

Matos, Tiago, Helena Caria, Joana Rita Chora, et al.. (2013). Spectrum and frequency ofGJB2mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients. International Journal of Audiology. 52(7). 466–471. 16 indexed citations

11.

Matos, Tiago, et al.. (2013). Isolation of PCR DNA fragments using aqueous two-phase systems. Separation and Purification Technology. 122. 144–148. 41 indexed citations

12.

Chora, Joana Rita, et al.. (2012). A novel p.Leu213X mutation in GJB2 gene in a Portuguese family. International Journal of Pediatric Otorhinolaryngology. 77(1). 89–91. 1 indexed citations

13.

Johansson, Hans-Olof, Tiago Matos, Juliana Silva da Luz, et al.. (2012). Plasmid DNA partitioning and separation using poly(ethylene glycol)/poly(acrylate)/salt aqueous two-phase systems. Journal of Chromatography A. 1233. 30–35. 28 indexed citations

14.

Matos, Tiago, O Dias, Mário Andrea, et al.. (2011). Novel splice-site mutation c.1615-2A>G (IVS14-2A>G) in the SLC26A4 gene causing Pendred syndrome in a consanguineous Portuguese family. American Journal of Medical Genetics Part A. 155(4). 924–927. 4 indexed citations

15.

Matos, Tiago, Helena Caria, Rita Cascão, et al.. (2011). Assessing Noncoding Sequence Variants of GJB2 for Hearing Loss Association. SHILAP Revista de lepidopterología. 2011. 1–8. 8 indexed citations

16.

Chora, Joana Rita, et al.. (2010). DFNB1-associated deafness in Portuguese cochlear implant users: Prevalence and impact on oral outcome. International Journal of Pediatric Otorhinolaryngology. 74(10). 1135–1139. 19 indexed citations

17.

Matos, Tiago, et al.. (2009). The Controversial p.Arg127His Mutation in GJB2 : Report on Three Portuguese Hearing Loss Family Cases. Genetic Testing and Molecular Biomarkers. 14(1). 141–144. 13 indexed citations

18.

Matos, Tiago, Helena Caria, Trond Aasen, et al.. (2008). A novel M163L mutation in connexin 26 causing cell death and associated with autosomal dominant hearing loss. Hearing Research. 240(1-2). 87–92. 29 indexed citations

19.

Sousa, Fani, Tiago Matos, D.M.F. Prazeres, & João A. Queiroz. (2007). Specific recognition of supercoiled plasmid DNA in arginine affinity chromatography. Analytical Biochemistry. 374(2). 432–434. 53 indexed citations

20.

Caria, Helena, Tiago Matos, Rui Oliveira Soares, et al.. (2005). A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma. Journal of the European Academy of Dermatology and Venereology. 19(4). 455–458. 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.

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