James S. Friedman
- Molecular Biology top 10%
- Ophthalmology top 2%
- Cellular and Molecular Neuroscience top 10%
- Cell Biology top 10%
- Genetics
- Co-authors
- Anand SwaroopTiziana CogliatiElspeth A. BrufordMichael A. WalterKoji M. NishiguchiDavid HicksShirley HeAlan J. Mears
- Topics
- Retinal Development and Disorders (13 papers)Photoreceptor and optogenetics research (5 papers)Retinoids in leukemia and cellular processes (4 papers)
- Journals
- Proceedings of the National Academy of SciencesJournal of Biological ChemistryThe American Journal of Human Genetics
- Partner nations
- United StatesCanadaJapan
In The Last Decade
James S. Friedman
20 papers receiving 928 citations
Peers
Comparison fields: 5 of 79
- Molecular Biology 793
- Ophthalmology 257
- Cellular and Molecular Neuroscience 255
- Cell Biology 131
- Genetics 113
Countries citing papers authored by James S. Friedman
This map shows the geographic impact of James S. Friedman'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 James S. Friedman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James S. Friedman more than expected).
Fields of papers citing papers by James S. Friedman
This network shows the impact of papers produced by James S. Friedman. 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 James S. Friedman. The network helps show where James S. Friedman may publish in the future.
Co-authorship network of co-authors of James S. Friedman
This figure shows the co-authorship network connecting the top 25 collaborators of James S. Friedman. A scholar is included among the top collaborators of James S. Friedman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with James S. Friedman. James S. Friedman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Genomewide search for genetic modifiers in patients with Leber congenital amaurosis using whole exome sequencing | 1 |
| 2 | 184 | |
| 3 | Loss of Lysophosphatidylcholine Acyltransferase 1 (LPCAT1) Leads to Photoreceptor Degeneration in rd11 Mice | 1 |
| 4 | 64 | |
| 5 | 48 | |
| 6 | Canine Rod Cone Dysplasia Type 2 (rcd2) Is the Canine Ortholog of Human and Murine RD3 | 2 |
| 7 | 44 | |
| 8 | 11 | |
| 9 | 56 | |
| 10 | 95 | |
| 11 | 49 | |
| 12 | 32 | |
| 13 | 144 | |
| 14 | 79 | |
| 15 | 33 | |
| 16 | 2 | |
| 17 | 33 | |
| 18 | Isolation of a novel iris-specific and leucine-rich repeat protein (oculoglycan) using differential selection. | 25 |
| 19 | 20 | |
| 20 | 12 |
About James S. Friedman
James S. Friedman is a scholar working on Ophthalmology, Cellular and Molecular Neuroscience and Molecular Biology, having authored 20 papers that have together received 935 indexed citations. Recurring topics across this work include Retinal Development and Disorders (13 papers), Photoreceptor and optogenetics research (5 papers) and Retinoids in leukemia and cellular processes (4 papers). The work is most often cited by research in Ophthalmology (257 citations), Cellular and Molecular Neuroscience (255 citations) and Molecular Biology (793 citations). James S. Friedman has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Anand Swaroop, Tiziana Cogliati, Elspeth A. Bruford, Michael A. Walter, Koji M. Nishiguchi, David Hicks, Shirley He, Alan J. Mears, Masayuki Akimoto and Vincent Raymond. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry 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.