Manir Ali
Impact in
- Ophthalmology top 2%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
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- Corneal surgery and disorders
- Corneal Surgery and Treatments
- Retinal Imaging and Analysis
Papers in
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- Retinal Development and Disorders 17
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- Retinal Diseases and Treatments 10
- Glaucoma and retinal disorders 4
- Co-authors
- Chris F. Inglehearn (38 shared papers)Timothy M. Cox (7 shared papers)Peter Rellos (3 shared papers)Martin McKibbin (22 shared papers)Carmel Toomes (18 shared papers)P.M. Hocking (10 shared papers)Alexander F. Markham (8 shared papers)Erica di Martino (1 shared paper)
- Journals
- Investigative Ophthalmology & Visual Science (9 papers)Journal of Medical Genetics (3 papers)Human Mutation (3 papers)PLoS ONE (3 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesEgypt
In The Last Decade
Manir Ali
60 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 103
- Ophthalmology 302
- Radiology, Nuclear Medicine and Imaging 356
- Genetics 277
- Clinical Biochemistry 67
- Endocrinology, Diabetes and Metabolism 160
Countries citing papers authored by Manir Ali
This map shows the geographic impact of Manir Ali'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 Manir Ali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manir Ali more than expected).
Fields of papers citing papers by Manir Ali
This network shows the impact of papers produced by Manir Ali. 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 Manir Ali. The network helps show where Manir Ali may publish in the future.
Co-authors
The 25 scholars most cited alongside Manir Ali, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 110 | |
| 2 | 2011 | 90 | |
| 3 | 2000 | 80 | |
| 4 | 2017 | 66 | |
| 5 | 2012 | 61 | |
| 6 | 2019 | 56 | |
| 7 | 2007 | 55 | |
| 8 | 2017 | 38 | |
| 9 | 1992 | 37 | |
| 10 | 2013 | 37 | |
| 11 | 2005 | 35 | |
| 12 | 1996 | 35 | |
| 13 | 2001 | 34 | |
| 14 | 2005 | 33 | |
| 15 | Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma. | 2010 | 33 |
| 16 | 2017 | 32 | |
| 17 | A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. | 2008 | 32 |
| 18 | 2006 | 31 | |
| 19 | 2014 | 31 | |
| 20 | 2009 | 29 |
About Manir Ali
Manir Ali is a scholar working on Molecular Biology, Ophthalmology, Radiology, Nuclear Medicine and Imaging, Genetics and Cell Biology, having authored 61 papers that have together received 1.4k indexed citations. Recurring topics across this work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (10 papers), Diet, Metabolism, and Disease (6 papers), Corneal surgery and disorders (6 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Corneal Surgery and Treatments (5 papers) and Glaucoma and retinal disorders (4 papers). The work is most often cited by research in Ophthalmology (302 citations), Radiology, Nuclear Medicine and Imaging (356 citations), Genetics (277 citations), Clinical Biochemistry (67 citations) and Endocrinology, Diabetes and Metabolism (160 citations). Manir Ali has collaborated with scholars based in United Kingdom, United States and Egypt. Frequent co-authors include Chris F. Inglehearn, Timothy M. Cox, Peter Rellos, Martin McKibbin, Carmel Toomes, P.M. Hocking, Alexander F. Markham, Erica di Martino, John D. Isaacs and James A. Poulter. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Journal of Medical Genetics, Human Mutation, PLoS ONE and European Journal of Medical 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.