Hadas Newman
About
In The Last Decade
Hadas Newman
31 papers receiving 500 citations
Peers
Comparison fields: 5 of 61
- Ophthalmology 293
- Molecular Biology 186
- Infectious Diseases 75
- Radiology, Nuclear Medicine and Imaging 64
- Genetics 57
Countries citing papers authored by Hadas Newman
This map shows the geographic impact of Hadas Newman'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 Hadas Newman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hadas Newman more than expected).
Fields of papers citing papers by Hadas Newman
This network shows the impact of papers produced by Hadas Newman. 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 Hadas Newman. The network helps show where Hadas Newman may publish in the future.
Co-authorship network of co-authors of Hadas Newman
This figure shows the co-authorship network connecting the top 25 collaborators of Hadas Newman. A scholar is included among the top collaborators of Hadas Newman 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 Hadas Newman. Hadas Newman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 4 | |
| 3 | 15 | |
| 4 | 1 | |
| 5 | 8 | |
| 6 | 8 | |
| 7 | 25 | |
| 8 | 13 | |
| 9 | 2 | |
| 10 | 29 | |
| 11 | 9 | |
| 12 | 36 | |
| 13 | 4 | |
| 14 | A combination of oculopharyngeal muscular dystrophy and a variant of enhanced S-cone syndrome in Bukharan Jews due to linked mutations in PABPN1 and NRL | 1 |
| 15 | 23 | |
| 16 | 29 | |
| 17 | An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy. | 22 |
| 18 | 1 | |
| 19 | Subfoveal Choroidal Melanoma: Pretreatment Characteristics and Response To Plaque Radiation Therapy | 2 |
| 20 | 20 |
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.