Françoise Meire
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments 7
- Intraocular Surgery and Lenses 6
- Sensory Systems top 5%
- Molecular Biology top 5%
- Retinal Development and Disorders 18
- Mitochondrial Function and Pathology 8
- Connexins and lens biology 6
- Genetics top 5%
- Ocular Disorders and Treatments 12
- Connective tissue disorders research 10
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- Metabolism and Genetic Disorders 5
- Co-authors
- Ann HallemansEls OrtibusElfride De BaerePeter AertsFrauke CoppietersJ.W. DellemanMaria M. van GenderenBart P. Leroy
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Françoise Meire
70 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 112
- Ophthalmology 677
- Physical Therapy, Sports Therapy and Rehabilitation 108
- Sensory Systems 108
- Molecular Biology 1.3k
- Genetics 487
Countries citing papers authored by Françoise Meire
This map shows the geographic impact of Françoise Meire'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 Françoise Meire with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Françoise Meire more than expected).
Fields of papers citing papers by Françoise Meire
This network shows the impact of papers produced by Françoise Meire. 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 Françoise Meire. The network helps show where Françoise Meire may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Françoise Meire, 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 | 2014 | 17 | |
| 2 | Homozygous deletion of glutamate receptor gene GRID2 causes new human hotfoot mutant phenotype, characterized by early-onset cerebellar ataxia and retinal dystrophy | 2014 | 2 |
| 3 | 2012 | 134 | |
| 4 | 2011 | 66 | |
| 5 | 2010 | 75 | |
| 6 | 2010 | 156 | |
| 7 | 2010 | 110 | |
| 8 | 2008 | 8 | |
| 9 | 2001 | 16 | |
| 10 | 2001 | 34 | |
| 11 | 1998 | 13 | |
| 12 | 1997 | 20 | |
| 13 | Kinderen met een visuele handicap | 1995 | 1 |
| 14 | 1995 | 30 | |
| 15 | Familial exudative vitreoretinopathy. | 1994 | 1 |
| 16 | 1994 | 19 | |
| 17 | 1994 | 14 | |
| 18 | 1992 | 10 | |
| 19 | Ocular manifestations of congenital Marfan syndrome with contractures. | 1991 | 0 |
| 20 | 1985 | 27 |
About Françoise Meire
Françoise Meire is a scholar working on Ophthalmology, Genetics and Developmental Biology, having authored 72 papers that have together received 2.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (18 papers), Ocular Disorders and Treatments (12 papers), Connective tissue disorders research (10 papers), Mitochondrial Function and Pathology (8 papers), Retinal Diseases and Treatments (7 papers), Intraocular Surgery and Lenses (6 papers), Connexins and lens biology (6 papers) and Metabolism and Genetic Disorders (5 papers). The work is most often cited by research in Ophthalmology (677 citations), Physical Therapy, Sports Therapy and Rehabilitation (108 citations) and Sensory Systems (108 citations). Françoise Meire has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Ann Hallemans, Els Ortibus, Elfride De Baere, Peter Aerts, Frauke Coppieters, J.W. Delleman, Maria M. van Genderen, Bart P. Leroy, Nicole Van Regemorter and Frans C. C. Riemslag. Their work appears in journals such as Ophthalmic Genetics, Human Mutation, Genetics in Medicine, The American Journal of Human Genetics 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.