Carmen Ramos
- Molecular Biology
- Genetics top 10%
- Ophthalmology top 5%
- Genetics top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Co-authors
- Carmen AyusoJavier Benı́tezRaúl SanzJuan A. ReyM. Josefa BelloM.Elena KusakIsabel Lorda‐SánchezPaola Bovolenta
- Topics
- Retinal Development and Disorders (9 papers)Genomic variations and chromosomal abnormalities (7 papers)Prenatal Screening and Diagnostics (6 papers)
- Cited by
- OphthalmologyGenetics
- Partner nations
- SpainUnited StatesNetherlands
In The Last Decade
Carmen Ramos
32 papers receiving 691 citations
Peers
Comparison fields: 5 of 72
- Molecular Biology 450
- Genetics 268
- Ophthalmology 125
- Genetics 105
- Pediatrics, Perinatology and Child Health 94
Countries citing papers authored by Carmen Ramos
This map shows the geographic impact of Carmen Ramos'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 Carmen Ramos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carmen Ramos more than expected).
Fields of papers citing papers by Carmen Ramos
This network shows the impact of papers produced by Carmen Ramos. 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 Carmen Ramos. The network helps show where Carmen Ramos may publish in the future.
Co-authorship network of co-authors of Carmen Ramos
This figure shows the co-authorship network connecting the top 25 collaborators of Carmen Ramos. A scholar is included among the top collaborators of Carmen Ramos 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 Carmen Ramos. Carmen Ramos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 8 | |
| 2 | 26 | |
| 3 | 1 | |
| 4 | 32 | |
| 5 | Early noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosis. | 10 |
| 6 | 23 | |
| 7 | 46 | |
| 8 | 24 | |
| 9 | 6 | |
| 10 | 6 | |
| 11 | A maternal inherited translocation t(1;22)(q11;p11) in two infertile brothers. | 5 |
| 12 | 17 | |
| 13 | 9 | |
| 14 | 33 | |
| 15 | 126 | |
| 16 | 4 | |
| 17 | 13 | |
| 18 | 14 | |
| 19 | 14 | |
| 20 | 112 |
About Carmen Ramos
Carmen Ramos is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 32 papers that have together received 720 indexed citations. Recurring topics across this work include Retinal Development and Disorders (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Ophthalmology (125 citations), Genetics (105 citations) and Genetics (268 citations). Carmen Ramos has collaborated with scholars based in Spain, United States and Netherlands. Frequent co-authors include Carmen Ayuso, Javier Benı́tez, Raúl Sanz, Juan A. Rey, M. Josefa Bello, M.Elena Kusak, Isabel Lorda‐Sánchez, Paola Bovolenta, Javier López-Rı́os and M. Esther Gallardo. Their work appears in journals such as Investigative Ophthalmology & Visual Science, British Journal of Ophthalmology and Genomics.
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.