Emma Borràs
Impact in
- Ophthalmology top 10%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
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- Cancer Genomics and Diagnostics
Papers in
-
- Advanced biosensing and bioanalysis techniques 4
- Retinal Development and Disorders 4
- CRISPR and Genetic Engineering 3
- Biochemical and Molecular Research 2
- Oncology 4
- Colorectal Cancer Treatments and Studies 2
- Co-authors
- Miguel Carballo (12 shared papers)Imma Hernán (11 shared papers)María José Gamundi (7 shared papers)Miguel Dias (8 shared papers)José A. G. Agúndez (4 shared papers)Miguel Blanca (3 shared papers)Àngels Arcusa (3 shared papers)Xavier Parés (3 shared papers)
- Journals
- Frontiers in Genetics (2 papers)Clinical Genetics (2 papers)Clinical & Translational Oncology (1 paper)BMC Genomics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- SpainUnited StatesPoland
In The Last Decade
Emma Borràs
17 papers receiving 311 citations
Peers
Comparison fields: 5 of 69
- Ophthalmology 46
- Cancer Research 62
- Oncology 74
- Molecular Biology 174
- Pharmacology 22
Countries citing papers authored by Emma Borràs
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
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.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 68 | |
| 2 | 2009 | 54 | |
| 3 | 2012 | 40 | |
| 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. | 2013 | 29 |
| 5 | Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing. | 2013 | 21 |
| 6 | 2011 | 20 | |
| 7 | 2012 | 18 | |
| 8 | 2011 | 14 | |
| 9 | 2013 | 10 | |
| 10 | 2005 | 8 | |
| 11 | 2013 | 8 | |
| 12 | 2014 | 6 | |
| 13 | 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. | 2015 | 6 |
| 14 | 2024 | 5 | |
| 15 | 2015 | 3 | |
| 16 | 2024 | 1 | |
| 17 | 2024 | 1 |
About Emma Borràs
Emma Borràs is a scholar working on Molecular Biology, Oncology, Genetics, Pathology and Forensic Medicine and Ophthalmology, having authored 17 papers that have together received 312 indexed citations. Recurring topics across this work include Advanced biosensing and bioanalysis techniques (4 papers), Retinal Development and Disorders (4 papers), CRISPR and Genetic Engineering (3 papers), Colorectal Cancer Treatments and Studies (2 papers), Genetic factors in colorectal cancer (2 papers), Glaucoma and retinal disorders (2 papers), BRCA gene mutations in cancer (2 papers) and Biochemical and Molecular Research (2 papers). The work is most often cited by research in Ophthalmology (46 citations), Cancer Research (62 citations), Oncology (74 citations), Molecular Biology (174 citations) and Pharmacology (22 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, Xavier Parés, Ester Planas‐Rigol and Jaume Farrés. Their work appears in journals such as Frontiers in Genetics, Clinical Genetics, Clinical & Translational Oncology, BMC Genomics and European Journal of Human Genetics.
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.