Walter W. Noll
- Molecular Biology top 10%
- Genetics top 5%
- Oncology top 10%
- Epidemiology top 10%
- Pulmonary and Respiratory Medicine top 10%
- Co-authors
- Bernard F. ColeDorothy R. BelloniDoris H. Wurster‐HillLeila A. MottAndrew J. SaykinCharlotte T. FurstenbergTim A. AhlesStephen Guerin
- Topics
- Genomic variations and chromosomal abnormalities (7 papers)Thyroid Cancer Diagnosis and Treatment (5 papers)Neuroendocrine Tumor Research Advances (4 papers)
- Partner nations
- United StatesFranceAustralia
In The Last Decade
Walter W. Noll
41 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 112
- Molecular Biology 770
- Genetics 507
- Oncology 438
- Epidemiology 354
- Pulmonary and Respiratory Medicine 298
Countries citing papers authored by Walter W. Noll
This map shows the geographic impact of Walter W. Noll'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 Walter W. Noll with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Walter W. Noll more than expected).
Fields of papers citing papers by Walter W. Noll
This network shows the impact of papers produced by Walter W. Noll. 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 Walter W. Noll. The network helps show where Walter W. Noll may publish in the future.
Co-authorship network of co-authors of Walter W. Noll
This figure shows the co-authorship network connecting the top 25 collaborators of Walter W. Noll. A scholar is included among the top collaborators of Walter W. Noll 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 Walter W. Noll. Walter W. Noll 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 | 275 | |
| 3 | 13 | |
| 4 | 259 | |
| 5 | 99 | |
| 6 | 30 | |
| 7 | 42 | |
| 8 | 17 | |
| 9 | 22 | |
| 10 | 21 | |
| 11 | 201 | |
| 12 | 44 | |
| 13 | 14 | |
| 14 | 4 | |
| 15 | 0 | |
| 16 | 30 | |
| 17 | 156 | |
| 18 | 9 | |
| 19 | 20 | |
| 20 | 2 |
About Walter W. Noll
Walter W. Noll is a scholar working on Genetics, Hematology and Genetics, having authored 43 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Thyroid Cancer Diagnosis and Treatment (5 papers) and Neuroendocrine Tumor Research Advances (4 papers). The work is most often cited by research in Genetics (255 citations), Genetics (507 citations) and Oncology (438 citations). Walter W. Noll has collaborated with scholars based in United States, France and Australia. Frequent co-authors include Bernard F. Cole, Dorothy R. Belloni, Doris H. Wurster‐Hill, Leila A. Mott, Andrew J. Saykin, Charlotte T. Furstenberg, Tim A. Ahles, Stephen Guerin, Olive S. Pettengill and Diane M. Harper. Their work appears in journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Biological Chemistry.
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.