Ryan Noss
Impact in
- Health Informatics top 10%
- Artificial Intelligence in Healthcare and Education
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic and rare skin diseases.
Papers in
- Genetics 10
- BRCA gene mutations in cancer 9
- Genetic and rare skin diseases. 1
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- Genetic factors in colorectal cancer 2
- Co-authors
- Robert Pilarski (2 shared papers)Julie A. Stephens (1 shared paper)James L. Fisher (1 shared paper)T. Prior (1 shared paper)Holly Jane Pederson (5 shared papers)Charis Eng (6 shared papers)Stephanie A. Cohen (1 shared paper)Samantha E. Greenberg (1 shared paper)
- Journals
- Annals of Surgical Oncology (2 papers)Breast Cancer Research and Treatment (2 papers)Journal of the American College of Surgeons (1 paper)npj Genomic Medicine (1 paper)Clinical and Translational Science (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Ryan Noss
16 papers receiving 422 citations
Peers
Comparison fields: 5 of 56
- Health Informatics 26
- Genetics 193
- Pathology and Forensic Medicine 69
- General Health Professions 42
- Public Health, Environmental and Occupational Health 52
Countries citing papers authored by Ryan Noss
This map shows the geographic impact of Ryan Noss'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 Ryan Noss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan Noss more than expected).
Fields of papers citing papers by Ryan Noss
This network shows the impact of papers produced by Ryan Noss. 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 Ryan Noss. The network helps show where Ryan Noss may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan Noss, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 123 | |
| 2 | 2020 | 53 | |
| 3 | 2023 | 41 | |
| 4 | 2024 | 41 | |
| 5 | 2018 | 38 | |
| 6 | 2016 | 28 | |
| 7 | 2019 | 28 | |
| 8 | 2018 | 20 | |
| 9 | 2011 | 18 | |
| 10 | 2017 | 11 | |
| 11 | 2022 | 10 | |
| 12 | 2020 | 9 | |
| 13 | 2020 | 7 | |
| 14 | 2014 | 3 | |
| 15 | 2022 | 3 | |
| 16 | 2023 | 1 | |
| 17 | 2023 | 0 |
About Ryan Noss
Ryan Noss is a scholar working on Genetics, Pathology and Forensic Medicine, General Health Professions, Pharmacology and Ophthalmology, having authored 17 papers that have together received 434 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (9 papers), Telemedicine and Telehealth Implementation (2 papers), Nursing Roles and Practices (2 papers), Genetic factors in colorectal cancer (2 papers), Genetics, Bioinformatics, and Biomedical Research (1 paper), Pharmacogenetics and Drug Metabolism (1 paper), Ocular Oncology and Treatments (1 paper) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Health Informatics (26 citations), Genetics (193 citations), Pathology and Forensic Medicine (69 citations), General Health Professions (42 citations) and Public Health, Environmental and Occupational Health (52 citations). Ryan Noss has collaborated with scholars based in United States and Canada. Frequent co-authors include Robert Pilarski, Julie A. Stephens, James L. Fisher, T. Prior, Holly Jane Pederson, Charis Eng, Stephanie A. Cohen, Samantha E. Greenberg, Stephen R. Grobmyer and Anne L. Matthews. Their work appears in journals such as Annals of Surgical Oncology, Breast Cancer Research and Treatment, Journal of the American College of Surgeons, npj Genomic Medicine and Clinical and Translational Science.
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.