Nancy Hanson
Impact in
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- Nuclear Structure and Function
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- RNA regulation and disease
Papers in
- Genetics 5
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 2
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- Nuclear Structure and Function 2
- DNA Repair Mechanisms 1
- Co-authors
- Junko Oshima (2 shared papers)Shahzad I. Mian (2 shared papers)Lishan Chen (1 shared paper)Brian K. Kennedy (2 shared papers)George M. Martin (1 shared paper)Yousef Shafeghati (2 shared papers)Abhimanyu Garg (1 shared paper)Eleanor G. Botha (2 shared papers)
- Journals
- Genetics in Medicine (1 paper)Gynecologic Oncology (1 paper)The Lancet (1 paper)Cancer (1 paper)Behavioral Medicine (1 paper)
- Partner nations
- United StatesAustriaGermany
In The Last Decade
Nancy Hanson
10 papers receiving 497 citations
Peers
Comparison fields: 5 of 56
- Molecular Biology 346
- Aging 7
- Cancer Research 43
- Pathology and Forensic Medicine 50
- Dermatology 25
Countries citing papers authored by Nancy Hanson
This map shows the geographic impact of Nancy Hanson'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 Hanson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy Hanson more than expected).
Fields of papers citing papers by Nancy Hanson
This network shows the impact of papers produced by Nancy Hanson. 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 Hanson. The network helps show where Nancy Hanson may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy Hanson, 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 | 2003 | 322 | |
| 2 | 2014 | 82 | |
| 3 | 2002 | 57 | |
| 4 | 2014 | 12 | |
| 5 | 2011 | 12 | |
| 6 | 2004 | 8 | |
| 7 | 2016 | 5 | |
| 8 | 2012 | 5 | |
| 9 | 2001 | 1 | |
| 10 | LMNA mutations identify a new genetic subset of subjects with progeroid features of werner syndrome | 2003 | 1 |
| 11 | 2014 | 0 |
About Nancy Hanson
Nancy Hanson is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and General Health Professions, having authored 11 papers that have together received 505 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (2 papers), Nuclear Structure and Function (2 papers), Child Abuse and Trauma (1 paper), DNA Repair Mechanisms (1 paper), Cancer Genomics and Diagnostics (1 paper), Injury Epidemiology and Prevention (1 paper) and Telomeres, Telomerase, and Senescence (1 paper). The work is most often cited by research in Molecular Biology (346 citations), Aging (7 citations), Cancer Research (43 citations), Pathology and Forensic Medicine (50 citations) and Dermatology (25 citations). Nancy Hanson has collaborated with scholars based in United States, Austria and Germany. Frequent co-authors include Junko Oshima, Shahzad I. Mian, Lishan Chen, Brian K. Kennedy, George M. Martin, Yousef Shafeghati, Abhimanyu Garg, Eleanor G. Botha, Lin Lee and Brian A. Kudlow. Their work appears in journals such as Genetics in Medicine, Gynecologic Oncology, The Lancet, Cancer and Behavioral Medicine.
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.