R. Bashir
Impact in
-
- Photoreceptor and optogenetics research
- Genetic Neurodegenerative Diseases
- Nerve injury and regeneration
- Developmental Neuroscience top 10%
Papers in
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- Muscle Physiology and Disorders 8
- Retinal Development and Disorders 7
- Ubiquitin and proteasome pathways 2
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- Photoreceptor and optogenetics research 6
- Genetic Neurodegenerative Diseases 3
- Co-authors
- C.F. Inglehearn (6 shared papers)Douglas H. Lester (5 shared papers)Alan C. Bird (5 shared papers)Shoumo Bhattacharya (4 shared papers)Sharon Keers (4 shared papers)S. Britton (3 shared papers)Jessica Moss (2 shared papers)Louise V.B. Anderson (2 shared papers)
- Journals
- Neuromuscular Disorders (4 papers)Genomics (3 papers)Human Molecular Genetics (2 papers)Journal of Medical Genetics (1 paper)Journal of Hepatology (1 paper)
- Partner nations
- United KingdomItalyUnited States
In The Last Decade
R. Bashir
25 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 69
- Cellular and Molecular Neuroscience 433
- Developmental Neuroscience 56
- Molecular Biology 906
- Cell Biology 157
- Ophthalmology 65
Countries citing papers authored by R. Bashir
This map shows the geographic impact of R. Bashir'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 R. Bashir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. Bashir more than expected).
Fields of papers citing papers by R. Bashir
This network shows the impact of papers produced by R. Bashir. 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 R. Bashir. The network helps show where R. Bashir may publish in the future.
Co-authors
The 25 scholars most cited alongside R. Bashir, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 235 | |
| 2 | 1997 | 208 | |
| 3 | 1999 | 141 | |
| 4 | 1991 | 130 | |
| 5 | A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. | 1991 | 94 |
| 6 | 2014 | 85 | |
| 7 | 1990 | 55 | |
| 8 | 1996 | 40 | |
| 9 | 1996 | 39 | |
| 10 | 1990 | 28 | |
| 11 | Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity. | 1990 | 21 |
| 12 | 1996 | 17 | |
| 13 | 1984 | 13 | |
| 14 | Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families. | 1992 | 12 |
| 15 | 1992 | 8 | |
| 16 | Sturge-Weber syndrome. | 1983 | 6 |
| 17 | 1999 | 5 | |
| 18 | IDENTIFICATION OF NOVEL RHODOPSIN MUTATIONS IN PATIENTS WITH AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA | 1991 | 4 |
| 19 | 1992 | 4 | |
| 20 | 1996 | 3 |
About R. Bashir
R. Bashir is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Cell Biology and Genetics, having authored 25 papers that have together received 1.2k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (8 papers), Retinal Development and Disorders (7 papers), Photoreceptor and optogenetics research (6 papers), Cardiomyopathy and Myosin Studies (5 papers), Genetic Neurodegenerative Diseases (3 papers), Ubiquitin and proteasome pathways (2 papers), Retinopathy of Prematurity Studies (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (433 citations), Developmental Neuroscience (56 citations), Molecular Biology (906 citations), Cell Biology (157 citations) and Ophthalmology (65 citations). R. Bashir has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include C.F. Inglehearn, Douglas H. Lester, Alan C. Bird, Shoumo Bhattacharya, Sharon Keers, S. Britton, Jessica Moss, Louise V.B. Anderson, Kenneth Davison and I. Mahjneh. Their work appears in journals such as Neuromuscular Disorders, Genomics, Human Molecular Genetics, Journal of Medical Genetics and Journal of Hepatology.
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.