Nancy Hamel
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 26
- BRCA gene mutations in cancer 24
- Genomic variations and chromosomal abnormalities 4
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- DNA Repair Mechanisms 10
- Co-authors
- William D. Foulkes (52 shared papers)Pierre O. Chappuis (5 shared papers)Nora Wong (7 shared papers)Jean‐Sébastien Brunet (4 shared papers)Marc Tischkowitz (12 shared papers)Nelly Sabbaghian (8 shared papers)Louis R. Bégin (4 shared papers)John R. Goffin (2 shared papers)
- Journals
- British Journal of Cancer (5 papers)Cancer Research (4 papers)Clinical Genetics (4 papers)Journal of Medical Genetics (3 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Nancy Hamel
57 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 94
- Genetics 1.1k
- Cancer Research 548
- Pathology and Forensic Medicine 400
- Oncology 536
- Molecular Biology 1.1k
Countries citing papers authored by Nancy Hamel
This map shows the geographic impact of Nancy Hamel'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 Hamel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy Hamel more than expected).
Fields of papers citing papers by Nancy Hamel
This network shows the impact of papers produced by Nancy Hamel. 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 Hamel. The network helps show where Nancy Hamel may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy Hamel, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 323 | |
| 2 | 2004 | 311 | |
| 3 | 2007 | 165 | |
| 4 | TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: distinctive spectrum and structural distribution. | 2001 | 159 |
| 5 | 2011 | 156 | |
| 6 | 2007 | 109 | |
| 7 | 2012 | 106 | |
| 8 | 2010 | 98 | |
| 9 | 2003 | 82 | |
| 10 | 2015 | 68 | |
| 11 | 2010 | 67 | |
| 12 | 1996 | 65 | |
| 13 | 2000 | 54 | |
| 14 | 2019 | 53 | |
| 15 | 2013 | 52 | |
| 16 | 2012 | 49 | |
| 17 | 2008 | 45 | |
| 18 | 2003 | 44 | |
| 19 | 2015 | 44 | |
| 20 | 2008 | 39 |
About Nancy Hamel
Nancy Hamel is a scholar working on Genetics, Molecular Biology, Surgery, Oncology and Pathology and Forensic Medicine, having authored 60 papers that have together received 2.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (24 papers), DNA Repair Mechanisms (10 papers), Congenital Diaphragmatic Hernia Studies (6 papers), Genetic factors in colorectal cancer (5 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Breast Cancer Treatment Studies (3 papers) and Cancer-related Molecular Pathways (3 papers). The work is most often cited by research in Genetics (1.1k citations), Cancer Research (548 citations), Pathology and Forensic Medicine (400 citations), Oncology (536 citations) and Molecular Biology (1.1k citations). Nancy Hamel has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include William D. Foulkes, Pierre O. Chappuis, Nora Wong, Jean‐Sébastien Brunet, Marc Tischkowitz, Nelly Sabbaghian, Louis R. Bégin, John R. Goffin, Marc S. Greenblatt and Jeffrey P. Bond. Their work appears in journals such as British Journal of Cancer, Cancer Research, Clinical Genetics, Journal of Medical Genetics and European Journal of Human Genetics.
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.