Ryan Noss
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
Papers in
- Genetics 12
- BRCA gene mutations in cancer 10
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 2
- Nutrition, Genetics, and Disease 1
- Co-authors
- Robert Pilarski (2 shared papers)T. Prior (1 shared paper)Julie Stephens (1 shared paper)James L. Fisher (1 shared paper)Holly J. Pederson (5 shared papers)Charis Eng (6 shared papers)Samantha Greenberg (1 shared paper)Stephanie A. Cohen (1 shared paper)
- Journals
- Breast Cancer Research and Treatment (2 papers)Annals of Surgical Oncology (2 papers)npj Genomic Medicine (1 paper)Clinical and Translational Science (1 paper)SAE technical papers on CD-ROM/SAE technical paper series (1 paper)
- Partner nations
- United StatesGermany
In The Last Decade
Ryan Noss
16 papers receiving 343 citations
Peers
Comparison fields: 5 of 67
- Genetics 175
- Health Informatics 6
- Pathology and Forensic Medicine 36
- Cancer Research 30
- Pediatrics, Perinatology and Child Health 36
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 | 99 | |
| 2 | 2020 | 48 | |
| 3 | 2018 | 35 | |
| 4 | 2023 | 34 | |
| 5 | 2016 | 28 | |
| 6 | 2019 | 26 | |
| 7 | 2018 | 19 | |
| 8 | 2011 | 16 | |
| 9 | 2017 | 10 | |
| 10 | 2022 | 10 | |
| 11 | 2020 | 8 | |
| 12 | 2020 | 6 | |
| 13 | 2003 | 4 | |
| 14 | 2014 | 3 | |
| 15 | 2022 | 2 | |
| 16 | 2023 | 1 | |
| 17 | 2023 | 0 |
About Ryan Noss
Ryan Noss is a scholar working on Genetics, Molecular Biology, Sociology and Political Science, Public Health, Environmental and Occupational Health and Automotive Engineering, having authored 17 papers that have together received 349 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (5 papers), Family Support in Illness (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Pharmacogenetics and Drug Metabolism (1 paper), Cancer Genomics and Diagnostics (1 paper), Nutrition, Genetics, and Disease (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Genetics (175 citations), Health Informatics (6 citations), Pathology and Forensic Medicine (36 citations), Cancer Research (30 citations) and Pediatrics, Perinatology and Child Health (36 citations). Ryan Noss has collaborated with scholars based in United States and Germany. Frequent co-authors include Robert Pilarski, T. Prior, Julie Stephens, James L. Fisher, Holly J. Pederson, Charis Eng, Samantha Greenberg, Stephanie A. Cohen, Stephen R. Grobmyer and Anna L. Mitchell. Their work appears in journals such as Breast Cancer Research and Treatment, Annals of Surgical Oncology, npj Genomic Medicine, Clinical and Translational Science and SAE technical papers on CD-ROM/SAE technical paper series.
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.