Emma Borràs

18 papers receiving 325 citations

Peers

Emma Borràs
Comparison fields: 5 of 66
  • Ophthalmology 33
  • Cancer Research 53
  • Pharmacology 24
  • Oncology 69
  • Molecular Biology 154
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Chenming Zeng China
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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-authors

The 25 scholars most cited alongside Emma Borràs, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Emma Borràs Line = papers co-authored together Emma Borràs links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 201169
2 200957
3 201242
4
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.
201331
5
Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing.
201321
6 201220
7 201120
8 201114
9 201310
10 20139
11 20058
12 20246
13 20146
14
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.
20156
15 20153
16 20012
17 20241
18 20241

About Emma Borràs

Emma Borràs is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Oncology, Ophthalmology and Genetics, having authored 18 papers that have together received 326 indexed citations. Recurring topics across this work include Retinal Development and Disorders (5 papers), DNA Repair Mechanisms (2 papers), BRCA gene mutations in cancer (2 papers), Glaucoma and retinal disorders (2 papers), Genetic factors in colorectal cancer (2 papers), Pharmacogenetics and Drug Metabolism (1 paper), Retinal Diseases and Treatments (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Ophthalmology (33 citations), Cancer Research (53 citations), Pharmacology (24 citations), Oncology (69 citations) and Molecular Biology (154 citations). Emma Borràs has collaborated with scholars based in Spain, United States and Poland. Frequent co-authors include Miguel Carballo, Imma Hernán, María José Gamundi, Miguel Dias, José A. G. Agúndez, Miguel Blanca, Àngels Arcusa, Jaume Farrés, Xavier Parés and Ester Planas‐Rigol. Their work appears in journals such as Frontiers in Genetics, Clinical Genetics, European Journal of Human Genetics, BMC Cancer and Investigative Ophthalmology & Visual Science.

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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