Andreas Gal
Impact in
- Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
- Ophthalmology top 0.2%
- Retinal Diseases and Treatments
Papers in
-
- Retinal Development and Disorders 55
- Physiology 66
- Lysosomal Storage Disorders Research 56
- Co-authors
- Debra A. Thompson (12 shared papers)Ulrike Orth (26 shared papers)Michael Beck (25 shared papers)E. Schwinger (23 shared papers)Susanna Bunge (20 shared papers)Eckart Apfelstedt-Sylla (10 shared papers)Catharina Whybra (11 shared papers)Ulrich Finckh (16 shared papers)
- Journals
- Human Mutation (27 papers)Nature Genetics (13 papers)Human Genetics (12 papers)Human Molecular Genetics (10 papers)The American Journal of Human Genetics (7 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Andreas Gal
224 papers receiving 11.8k citations
Andreas Gal's Hit Papers
Peers
Comparison fields: 5 of 138
- Sensory Systems 947
- Ophthalmology 1.5k
- Physiology 3.4k
- Molecular Biology 6.8k
- Cell Biology 1.5k
Countries citing papers authored by Andreas Gal
This map shows the geographic impact of Andreas Gal'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 Andreas Gal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Gal more than expected).
Fields of papers citing papers by Andreas Gal
This network shows the impact of papers produced by Andreas Gal. 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 Andreas Gal. The network helps show where Andreas Gal may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Gal, 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 228 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa Hit paper breakdown → | 2000 | 570 |
| 2 | Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy Hit paper breakdown → | 1997 | 545 |
| 3 | 2001 | 415 | |
| 4 | 2000 | 379 | |
| 5 | 2000 | 304 | |
| 6 | 2000 | 284 | |
| 7 | 1995 | 245 | |
| 8 | 2004 | 222 | |
| 9 | 2001 | 222 | |
| 10 | Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration. | 2000 | 220 |
| 11 | 2009 | 195 | |
| 12 | 1994 | 192 | |
| 13 | 2004 | 192 | |
| 14 | 2004 | 185 | |
| 15 | 1990 | 176 | |
| 16 | 2003 | 174 | |
| 17 | 1989 | 174 | |
| 18 | 2005 | 169 | |
| 19 | Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. | 2000 | 167 |
| 20 | 2003 | 167 |
About Andreas Gal
Andreas Gal is a scholar working on Molecular Biology, Physiology, Genetics, Cellular and Molecular Neuroscience and Ophthalmology, having authored 228 papers that have together received 12.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (56 papers), Retinal Development and Disorders (55 papers), Trypanosoma species research and implications (24 papers), Retinal Diseases and Treatments (23 papers), Photoreceptor and optogenetics research (22 papers), Glycogen Storage Diseases and Myoclonus (17 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Carbohydrate Chemistry and Synthesis (14 papers). The work is most often cited by research in Sensory Systems (947 citations), Ophthalmology (1.5k citations), Physiology (3.4k citations), Molecular Biology (6.8k citations) and Cell Biology (1.5k citations). Andreas Gal has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Debra A. Thompson, Ulrike Orth, Michael Beck, E. Schwinger, Susanna Bunge, Eckart Apfelstedt-Sylla, Catharina Whybra, Ulrich Finckh, Samuel G. Jacobson and Markus Ries. Their work appears in journals such as Human Mutation, Nature Genetics, Human Genetics, Human Molecular Genetics and The American Journal of Human 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.