Emma Borràs

650 total citations
17 papers, 312 citations indexed

About

Emma Borràs is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Emma Borràs has authored 17 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Oncology and 3 papers in Genetics. Recurrent topics in Emma Borràs's work include Advanced biosensing and bioanalysis techniques (4 papers), Retinal Development and Disorders (4 papers) and CRISPR and Genetic Engineering (3 papers). Emma Borràs is often cited by papers focused on Advanced biosensing and bioanalysis techniques (4 papers), Retinal Development and Disorders (4 papers) and CRISPR and Genetic Engineering (3 papers). Emma Borràs collaborates with scholars based in Spain, United States and Poland. Emma Borràs's co-authors include Miguel Carballo, Imma Hernán, María José Gamundi, Miguel Dias, José A. G. Agúndez, Miguel Blanca, Àngels Arcusa, Ester Planas‐Rigol, Xavier Parés and Jaume Farrés and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Investigative Ophthalmology & Visual Science.

In The Last Decade

Emma Borràs

17 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Borràs Spain 9 174 74 62 59 46 17 312
Chun‐Hua Wang Taiwan 14 385 2.2× 127 1.7× 100 1.6× 33 0.6× 4 0.1× 21 502
Poh Yong Ng Singapore 8 266 1.5× 58 0.8× 108 1.7× 41 0.7× 5 0.1× 8 462
K.W. Foreman United States 4 229 1.3× 63 0.9× 58 0.9× 40 0.7× 3 0.1× 4 350
Jianxin Yu China 12 181 1.0× 52 0.7× 18 0.3× 35 0.6× 5 0.1× 19 372
Shinsuke Araki Japan 11 323 1.9× 73 1.0× 59 1.0× 23 0.4× 5 0.1× 22 425
Chenming Zeng China 12 304 1.7× 60 0.8× 77 1.2× 9 0.2× 8 0.2× 22 440
Benjamin R. Topacio United States 5 214 1.2× 119 1.6× 34 0.5× 15 0.3× 9 0.2× 6 351
Thomas D. Hart United States 10 171 1.0× 180 2.4× 41 0.7× 39 0.7× 3 0.1× 13 361
Laurent Bermont France 11 207 1.2× 78 1.1× 54 0.9× 83 1.4× 7 0.2× 23 398

Countries citing papers authored by Emma Borràs

Since Specialization
Citations

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

Fields of papers citing papers by Emma Borràs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Borràs

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

All Works

17 of 17 papers shown
1.
Seplyarskiy, Vladimir B., Mariona Terradas, Pilar Mur, et al.. (2024). Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells. European Journal of Human Genetics. 32(7). 837–845. 5 indexed citations
2.
Totten, Vicken Y., Gisela Teixidó‐Turà, Paula Fernández‐Álvarez, et al.. (2024). Arterial aneurysm and dissection: toward the evolving phenotype of Tatton-Brown-Rahman syndrome. Journal of Medical Genetics. 61(9). 870–877. 1 indexed citations
3.
Millá, Elena, María José Gamundi, Emma Borràs, et al.. (2024). Next-generation sequencing-based gene panel tests for the detection of rare variants and hypomorphic alleles associated with primary open-angle glaucoma. PLoS ONE. 19(1). e0282133–e0282133. 1 indexed citations
4.
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
5.
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
6.
Borràs, Emma, Ricard Albalat, Gregg Duester, Xavier Parés, & Jaume Farrés. (2014). The Xenopusalcohol dehydrogenase gene family: characterization and comparative analysis incorporating amphibian and reptilian genomes. BMC Genomics. 15(1). 216–216. 6 indexed citations
7.
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
8.
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
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.
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
11.
Agúndez, José A. G., Francisco Abad‐Santos, Ana Aldea‐Perona, et al.. (2012). Toward a clinical practice guide in pharmacogenomics testing for functional polymorphisms of drug-metabolizing enzymes. Gene/drug pairs and barriers perceived in Spain. Frontiers in Genetics. 3. 273–273. 18 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.
Hernán, Imma, Emma Borràs, Blanca Garcı́a-Sandoval, et al.. (2011). Novel p.M96T variant of NRL and shRNA‐based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa. Clinical Genetics. 82(5). 446–452. 14 indexed citations
14.
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
15.
Hernán, Imma, et al.. (2011). Cellular Expression and siRNA-Mediated Interference of Rhodopsincis-Acting Splicing Mutants Associated with Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 52(6). 3723–3723. 20 indexed citations
16.
Porté, Sergio, Emma Borràs, N. Shafqat, et al.. (2009). Three-dimensional Structure and Enzymatic Function of Proapoptotic Human p53-inducible Quinone Oxidoreductase PIG3. Journal of Biological Chemistry. 284(25). 17194–17205. 54 indexed citations
17.
Domínguez, Marta, Rosana Álvarez, Emma Borràs, et al.. (2005). Synthesis of enantiopure C3- and C4-hydroxyretinals and their enzymatic reduction by ADH8 from Xenopus laevis. Organic & Biomolecular Chemistry. 4(1). 155–164. 8 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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