Irma López
Impact in
- Ophthalmology top 1%
- Retinal Diseases and Treatments
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
-
- Retinal Development and Disorders 23
-
- Retinal Diseases and Treatments 5
- Glaucoma and retinal disorders 2
- Co-authors
- Robert K. Koenekoop (28 shared papers)Frans P.M. Cremers (10 shared papers)Anneke I. den Hollander (9 shared papers)L. Ingeborgh van den Born (7 shared papers)Carel B. Hoyng (5 shared papers)Klaus Rohrschneider (4 shared papers)Suzanne Yzer (5 shared papers)Marijke N. Zonneveld (4 shared papers)
- Journals
- Investigative Ophthalmology & Visual Science (8 papers)Human Molecular Genetics (5 papers)The American Journal of Human Genetics (3 papers)Journal of Clinical Investigation (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- CanadaUnited StatesNetherlands
In The Last Decade
Irma López
35 papers receiving 2.0k citations
Irma López's Hit Papers
Peers
Comparison fields: 5 of 94
- Ophthalmology 468
- Sensory Systems 212
- Molecular Biology 1.6k
- Genetics 583
- Cell Biology 198
Countries citing papers authored by Irma López
This map shows the geographic impact of Irma López'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 Irma López with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irma López more than expected).
Fields of papers citing papers by Irma López
This network shows the impact of papers produced by Irma López. 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 Irma López. The network helps show where Irma López may publish in the future.
Co-authors
The 25 scholars most cited alongside Irma López, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis Hit paper breakdown → | 2006 | 512 |
| 2 | 2010 | 188 | |
| 3 | 2007 | 137 | |
| 4 | 2007 | 95 | |
| 5 | 1961 | 94 | |
| 6 | 2009 | 92 | |
| 7 | 2010 | 88 | |
| 8 | 2010 | 84 | |
| 9 | 2010 | 84 | |
| 10 | 2007 | 81 | |
| 11 | 2013 | 77 | |
| 12 | 2013 | 52 | |
| 13 | 2010 | 48 | |
| 14 | 2010 | 47 | |
| 15 | Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290. | 2012 | 43 |
| 16 | 2014 | 41 | |
| 17 | 2007 | 39 | |
| 18 | 2006 | 36 | |
| 19 | 2015 | 33 | |
| 20 | 2016 | 33 |
About Irma López
Irma López is a scholar working on Molecular Biology, Ophthalmology, Genetics, Sensory Systems and Cell Biology, having authored 36 papers that have together received 2.1k indexed citations. Recurring topics across this work include Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Genomics and Rare Diseases (3 papers), Cellular transport and secretion (2 papers), Glaucoma and retinal disorders (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Photoreceptor and optogenetics research (2 papers). The work is most often cited by research in Ophthalmology (468 citations), Sensory Systems (212 citations), Molecular Biology (1.6k citations), Genetics (583 citations) and Cell Biology (198 citations). Irma López has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Robert K. Koenekoop, Frans P.M. Cremers, Anneke I. den Hollander, L. Ingeborgh van den Born, Carel B. Hoyng, Klaus Rohrschneider, Suzanne Yzer, Marijke N. Zonneveld, Tim M. Strom and Thomas Meitinger. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Human Molecular Genetics, The American Journal of Human Genetics, Journal of Clinical Investigation and Genetics in Medicine.
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.