Nancy Press
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 22
- BRCA gene mutations in cancer 20
- Genomics and Rare Diseases 4
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- Prenatal Screening and Diagnostics 7
- Ethics and Legal Issues in Pediatric Healthcare 6
- Co-authors
- Carole H. Browner (9 shared papers)Wylie Burke (23 shared papers)Linda K. Ganzini (6 shared papers)Susan Markens (2 shared papers)Gloria M. Petersen (1 shared paper)Susan Miesfeldt (1 shared paper)Donald W. Hadley (1 shared paper)Karen H. Lu (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)Public Health Genomics (3 papers)Social Science & Medicine (3 papers)Journal of Palliative Medicine (3 papers)Obstetrics and Gynecology (2 papers)
- Partner nations
- United StatesCanadaSouth Africa
In The Last Decade
Nancy Press
57 papers receiving 2.7k citations
Nancy Press's Hit Papers
Peers
Comparison fields: 5 of 123
- Genetics 816
- Pediatrics, Perinatology and Child Health 509
- Hematology 306
- Pathology and Forensic Medicine 456
- Reproductive Medicine 177
Countries citing papers authored by Nancy Press
This map shows the geographic impact of Nancy Press'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 Press with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy Press more than expected).
Fields of papers citing papers by Nancy Press
This network shows the impact of papers produced by Nancy Press. 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 Press. The network helps show where Nancy Press may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy Press, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review. Hit paper breakdown → | 2006 | 501 |
| 2 | 1998 | 235 | |
| 3 | 1997 | 214 | |
| 4 | Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent. | 1997 | 177 |
| 5 | 1996 | 121 | |
| 6 | 2013 | 118 | |
| 7 | 1999 | 113 | |
| 8 | 2003 | 112 | |
| 9 | 2012 | 99 | |
| 10 | 2004 | 74 | |
| 11 | 2002 | 73 | |
| 12 | 1997 | 71 | |
| 13 | 1998 | 68 | |
| 14 | 2009 | 61 | |
| 15 | 2010 | 60 | |
| 16 | 2003 | 59 | |
| 17 | 2012 | 56 | |
| 18 | 2013 | 53 | |
| 19 | Heparin-steroid conjugates: new angiogenesis inhibitors with antitumor activity in mice. | 1993 | 48 |
| 20 | 2001 | 44 |
About Nancy Press
Nancy Press is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, General Health Professions and Hematology, having authored 58 papers that have together received 3.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (20 papers), Prenatal Screening and Diagnostics (7 papers), Ethics in Clinical Research (7 papers), Ethics and Legal Issues in Pediatric Healthcare (6 papers), Iron Metabolism and Disorders (5 papers), Global Cancer Incidence and Screening (5 papers), Ethics in medical practice (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (816 citations), Pediatrics, Perinatology and Child Health (509 citations), Hematology (306 citations), Pathology and Forensic Medicine (456 citations) and Reproductive Medicine (177 citations). Nancy Press has collaborated with scholars based in United States, Canada and South Africa. Frequent co-authors include Carole H. Browner, Wylie Burke, Linda K. Ganzini, Susan Markens, Gloria M. Petersen, Susan Miesfeldt, Donald W. Hadley, Karen H. Lu, Noralane M. Lindor and Anita Yeomans Kinney. Their work appears in journals such as Genetics in Medicine, Public Health Genomics, Social Science & Medicine, Journal of Palliative Medicine and Obstetrics and Gynecology.
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.