Miguel Dias

454 total citations
13 papers, 238 citations indexed

About

Miguel Dias is a scholar working on Molecular Biology, Ophthalmology and Oncology. According to data from OpenAlex, Miguel Dias has authored 13 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 2 papers in Ophthalmology and 2 papers in Oncology. Recurrent topics in Miguel Dias's work include Retinal Development and Disorders (5 papers), Advanced biosensing and bioanalysis techniques (3 papers) and CRISPR and Genetic Engineering (2 papers). Miguel Dias is often cited by papers focused on Retinal Development and Disorders (5 papers), Advanced biosensing and bioanalysis techniques (3 papers) and CRISPR and Genetic Engineering (2 papers). Miguel Dias collaborates with scholars based in Spain, France and Austria. Miguel Dias's co-authors include Miguel Carballo, Imma Hernán, Emma Borràs, María José Gamundi, José A. G. Agúndez, Miguel Blanca, Àngels Arcusa, Gerhart Braunegg, Martin Koller and Alejandra Rodríguez‐Contreras and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Thin Solid Films.

In The Last Decade

Miguel Dias

13 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miguel Dias Spain 8 114 55 51 46 42 13 238
Yuhua Tian China 9 146 1.3× 41 0.7× 34 0.7× 85 1.8× 13 0.3× 23 304
Alice Fiévet France 9 104 0.9× 57 1.0× 45 0.9× 39 0.8× 6 0.1× 15 187
Keith Wells United States 7 184 1.6× 187 3.4× 9 0.2× 57 1.2× 11 0.3× 11 364
Bárbara Marques Portugal 9 147 1.3× 39 0.7× 75 1.5× 34 0.7× 5 0.1× 19 272
Linus Lee United States 8 204 1.8× 82 1.5× 15 0.3× 59 1.3× 3 0.1× 29 317
Haochen Mou China 10 96 0.8× 66 1.2× 11 0.2× 52 1.1× 6 0.1× 17 265
Konstanze Stangner Germany 4 180 1.6× 90 1.6× 16 0.3× 35 0.8× 4 0.1× 5 283
Alexandra Faustino Portugal 9 164 1.4× 82 1.5× 30 0.6× 32 0.7× 6 0.1× 11 266

Countries citing papers authored by Miguel Dias

Since Specialization
Citations

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

Fields of papers citing papers by Miguel Dias

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miguel Dias

This figure shows the co-authorship network connecting the top 25 collaborators of Miguel Dias. A scholar is included among the top collaborators of Miguel Dias 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 Miguel Dias. Miguel Dias 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
1.
Orhan, Elise, Marion Neuillé, Miguel Dias, et al.. (2021). A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency. International Journal of Molecular Sciences. 22(9). 4424–4424. 5 indexed citations
2.
3.
Dias, Miguel, Christian P. Hamel, Isabelle Meunier, et al.. (2017). Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family.. PubMed. 23. 131–139. 9 indexed citations
4.
Dias, Miguel, Imma Hernán, Emma Borràs, et al.. (2015). New COL6A6 variant detected by whole-exome sequencing is linked to break points in intron 4 and 3'-UTR, deleting exon 5 of RHO, and causing adRP.. PubMed. 21. 857–70. 6 indexed citations
5.
Koller, Martin, Miguel Dias, Alejandra Rodríguez‐Contreras, et al.. (2015). Liquefied Wood as Inexpensive Precursor-Feedstock for Bio-Mediated Incorporation of (R)-3-Hydroxyvalerate into Polyhydroxyalkanoates. Materials. 8(9). 6543–6557. 32 indexed citations
6.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2015). Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancer. Clinical & Translational Oncology. 17(7). 576–580. 3 indexed citations
7.
Dias, Miguel, Tassia L. Junqueira, Mateus Ferreira Chagas, et al.. (2014). Production of Butanol and Other High Valued Chemicals Using Ethanol as Feedstock Integrated to a First and Second Generation Sugarcane Distillery. SHILAP Revista de lepidopterología. 5 indexed citations
8.
Millá, Elena, Susana Duch, Imma Hernán, et al.. (2013). Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.. PubMed. 19. 1707–22. 29 indexed citations
9.
Borràs, Emma, et al.. (2013). Detection of novel genetic variation in autosomal dominant retinitis pigmentosa. Clinical Genetics. 84(5). 441–452. 8 indexed citations
10.
Borràs, Emma, E. Dotor, Àngels Arcusa, et al.. (2013). High-resolution melting analysis of the common c.1905+1G>A mutation causing dihydropyrimidine dehydrogenase deficiency and lethal 5-fluorouracil toxicity. Frontiers in Genetics. 3. 312–312. 10 indexed citations
11.
Dias, Miguel, et al.. (2013). Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing.. PubMed. 19. 654–64. 21 indexed citations
12.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2012). Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing. Journal of Molecular Diagnostics. 14(3). 286–293. 40 indexed citations
13.
Borràs, Emma, Imma Hernán, María José Gamundi, et al.. (2011). Clinical pharmacogenomic testing of KRAS, BRAF and EGFRmutations by high resolution melting analysis and ultra-deep pyrosequencing. BMC Cancer. 11(1). 406–406. 68 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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