Stephen P. Daiger
About
In The Last Decade
Stephen P. Daiger
159 papers receiving 7.2k citations
Hit Papers
Peers
Comparison fields: 5 of 146
- Molecular Biology 5.8k
- Ophthalmology 2.1k
- Genetics 1.7k
- Cellular and Molecular Neuroscience 1.2k
- Cell Biology 821
Countries citing papers authored by Stephen P. Daiger
This map shows the geographic impact of Stephen P. Daiger'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 Stephen P. Daiger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen P. Daiger more than expected).
Fields of papers citing papers by Stephen P. Daiger
This network shows the impact of papers produced by Stephen P. Daiger. 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 Stephen P. Daiger. The network helps show where Stephen P. Daiger may publish in the future.
Co-authorship network of co-authors of Stephen P. Daiger
This figure shows the co-authorship network connecting the top 25 collaborators of Stephen P. Daiger. A scholar is included among the top collaborators of Stephen P. Daiger 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 Stephen P. Daiger. Stephen P. Daiger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | RUSH2A: systematic cohort variant modeling reveals phenotypic correlates | 1 |
| 2 | Multiple copies of rhodopsin as a novel cause of autosomal dominant retinitis pigmentosa | 1 |
| 3 | X-Chromosome Inactivation is a Biomarker of Clinical Severity in Female Carriers of X-linked Retinitis Pigmentosa | 1 |
| 4 | 29 | |
| 5 | 26 | |
| 6 | Complex Multi-Allelic Inherited Retinal Dystrophy: Multiple Genes Contributing Independently and Concurrently in Extended Families | 2 |
| 7 | Retinal Targeted-Capture Next Generation Sequencing and CLIA Confirmation in a Representative Range of Patients with Inherited Retinal Degeneration | 1 |
| 8 | 7 | |
| 9 | A novel locus for autosomal dominant retinitis pigmentosa (adRP) on chromosome 19q13 | 0 |
| 10 | 30 | |
| 11 | Variant prioritization and linkage mapping using whole-exome sequencing data for families with autosomal dominant retinitis pigmentosa (adRP) | 1 |
| 12 | Genome-Wide Linkage Analysis For Gene Discovery In Autosomal Dominant Retinitis Pigmentosa | 1 |
| 13 | High Resolution Retinal Images in a Family with Autosomal Dominant Retinitis Pigmentosa Caused By a Mutation in NR2E3 | 1 |
| 14 | Autosomal dominant retinitis pigmentosa: exclusion of known and mapped genes in three families. | 1 |
| 15 | Frequency and Spectrum of IMPDH1 Mutations Associated with Autosomal Dominant Retinitis Pigmentosa | 1 |
| 16 | 46 | |
| 17 | 220 | |
| 18 | Reply to Inglehearn and Hardcastle: The Map Is Not the Territory | 1 |
| 19 | Reply to Farrall et al | 2 |
| 20 | 59 |
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.