Nancy R. Schneider
- Molecular Biology
- Oncology top 10%
- Pathology and Forensic Medicine top 5%
- Genetics top 10%
- Hematology top 5%
- Co-authors
- Gail E. TomlinsonCharles F. TimmonsRobert W. McKennaVijay S. TonkArthur G. WeinbergKathleen WilsonD. Brian DawsonSteven H. Kroft
- Topics
- Genomic variations and chromosomal abnormalities (12 papers)Cancer Genomics and Diagnostics (7 papers)Chromosomal and Genetic Variations (7 papers)
- Journals
- BloodCancerEndocrinology
- Partner nations
- United StatesUnited KingdomGuatemala
In The Last Decade
Nancy R. Schneider
49 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 92
- Molecular Biology 581
- Oncology 364
- Pathology and Forensic Medicine 342
- Genetics 267
- Hematology 236
Countries citing papers authored by Nancy R. Schneider
This map shows the geographic impact of Nancy R. Schneider'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 Nancy R. Schneider with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy R. Schneider more than expected).
Fields of papers citing papers by Nancy R. Schneider
This network shows the impact of papers produced by Nancy R. Schneider. 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 Nancy R. Schneider. The network helps show where Nancy R. Schneider may publish in the future.
Co-authorship network of co-authors of Nancy R. Schneider
This figure shows the co-authorship network connecting the top 25 collaborators of Nancy R. Schneider. A scholar is included among the top collaborators of Nancy R. Schneider 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 Nancy R. Schneider. Nancy R. Schneider is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 10 | |
| 2 | 17 | |
| 3 | 49 | |
| 4 | 41 | |
| 5 | 35 | |
| 6 | 30 | |
| 7 | 16 | |
| 8 | 6 | |
| 9 | 39 | |
| 10 | 168 | |
| 11 | 17 | |
| 12 | 189 | |
| 13 | 52 | |
| 14 | 34 | |
| 15 | 33 | |
| 16 | 11 | |
| 17 | 20 | |
| 18 | 26 | |
| 19 | 3 | |
| 20 | 4 |
About Nancy R. Schneider
Nancy R. Schneider is a scholar working on Hematology, Genetics and Pathology and Forensic Medicine, having authored 49 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Cancer Genomics and Diagnostics (7 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Hematology (236 citations), Pathology and Forensic Medicine (342 citations) and Oncology (364 citations). Nancy R. Schneider has collaborated with scholars based in United States, United Kingdom and Guatemala. Frequent co-authors include Gail E. Tomlinson, Charles F. Timmons, Robert W. McKenna, Vijay S. Tonk, Arthur G. Weinberg, Kathleen Wilson, D. Brian Dawson, Steven H. Kroft, Golder N. Wilson and Perry D. Nisen. Their work appears in journals such as Blood, Cancer and Endocrinology.
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.