N. Torben Bech‐Hansen
About
In The Last Decade
N. Torben Bech‐Hansen
70 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 121
- Molecular Biology 1.6k
- Cellular and Molecular Neuroscience 739
- Oncology 291
- Ophthalmology 237
- Genetics 223
Countries citing papers authored by N. Torben Bech‐Hansen
This map shows the geographic impact of N. Torben Bech‐Hansen'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 N. Torben Bech‐Hansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Torben Bech‐Hansen more than expected).
Fields of papers citing papers by N. Torben Bech‐Hansen
This network shows the impact of papers produced by N. Torben Bech‐Hansen. 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 N. Torben Bech‐Hansen. The network helps show where N. Torben Bech‐Hansen may publish in the future.
Co-authorship network of co-authors of N. Torben Bech‐Hansen
This figure shows the co-authorship network connecting the top 25 collaborators of N. Torben Bech‐Hansen. A scholar is included among the top collaborators of N. Torben Bech‐Hansen 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 N. Torben Bech‐Hansen. N. Torben Bech‐Hansen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 14 | |
| 3 | Mutation Analysis in a Cohort of CSNB Patients: Novel Mutations in TRPM1 Gene | 1 |
| 4 | Phenotypic Variability in Genetically Defined X-linked Congenital Stationary Night Blindness | 2 |
| 5 | 28 | |
| 6 | 23 | |
| 7 | 27 | |
| 8 | Spatiotemporal Contrast Sensitivity Characteristics of Optokinetic Responses in Chicks and in Normal and Cacna1f-Mutant Mice | 3 |
| 9 | The Cacna1f-Mutant Retina Shows Evidence of Failed Synaptogenesis, Abnormal Synaptic Ribbon Structure and Increased Photoreceptor Cell Death | 1 |
| 10 | 57 | |
| 11 | 203 | |
| 12 | 4 | |
| 13 | Mutation of the Calcium Channel Gene Cacna1f Disrupts Calcium Signaling and Synaptic Transmission in Mouse Retina | 1 |
| 14 | Characterization of the Genotype and Phenotype of Congenital Stationary Night Blindness in Atlantic Canada | 1 |
| 15 | 1 | |
| 16 | 249 | |
| 17 | 30 | |
| 18 | 7 | |
| 19 | 7 | |
| 20 | 3 |
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.