Fergus J. Couch
Impact in
- Genetics top 0.02%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 168
- BRCA gene mutations in cancer 144
- Genomics and Rare Diseases 37
- Genomic variations and chromosomal abnormalities 23
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- DNA Repair Mechanisms 50
- CRISPR and Genetic Engineering 36
- Co-authors
- Sean V. Tavtigian (16 shared papers)Katherine L. Nathanson (16 shared papers)Álvaro N.A. Monteiro (28 shared papers)Barbara L. Weber (11 shared papers)Steven N. Hart (36 shared papers)James N. Ingle (19 shared papers)Kenneth Offit (14 shared papers)Judy E. Garber (12 shared papers)
- Journals
- Journal of Clinical Oncology (28 papers)Cancer Research (27 papers)Breast Cancer Research and Treatment (16 papers)Cancer Epidemiology Biomarkers & Prevention (14 papers)Human Mutation (13 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Fergus J. Couch
277 papers receiving 17.1k citations
Fergus J. Couch's Hit Papers
Peers
Comparison fields: 5 of 152
- Genetics 9.4k
- Cancer Research 5.0k
- Oncology 5.4k
- Pathology and Forensic Medicine 2.8k
- Molecular Biology 8.6k
Countries citing papers authored by Fergus J. Couch
This map shows the geographic impact of Fergus J. Couch'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 Fergus J. Couch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fergus J. Couch more than expected).
Fields of papers citing papers by Fergus J. Couch
This network shows the impact of papers produced by Fergus J. Couch. 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 Fergus J. Couch. The network helps show where Fergus J. Couch may publish in the future.
Co-authors
The 25 scholars most cited alongside Fergus J. Couch, 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 292 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Secondary mutations as a mechanism of cisplatin resistance in BRCA2-mutated cancers Hit paper breakdown → | 2008 | 792 |
| 2 | Control of BRCA2 Cellular and Clinical Functions by a Nuclear Partner, PALB2 Hit paper breakdown → | 2006 | 635 |
| 3 | Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk Hit paper breakdown → | 2015 | 579 |
| 4 | Pharmacogenetics of Tamoxifen Biotransformation Is Associated With Clinical Outcomes of Efficacy and Hot Flashes Hit paper breakdown → | 2005 | 567 |
| 5 | Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers Hit paper breakdown → | 2001 | 546 |
| 6 | BRCA1Mutations in Women Attending Clinics That Evaluate the Risk of Breast Cancer Hit paper breakdown → | 1997 | 506 |
| 7 | 1998 | 485 | |
| 8 | 2006 | 393 | |
| 9 | Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer Hit paper breakdown → | 2017 | 393 |
| 10 | Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer Hit paper breakdown → | 2018 | 345 |
| 11 | 2007 | 318 | |
| 12 | Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework Hit paper breakdown → | 2019 | 310 |
| 13 | 1994 | 307 | |
| 14 | 2009 | 302 | |
| 15 | 1993 | 271 | |
| 16 | 1996 | 270 | |
| 17 | 2008 | 261 | |
| 18 | 2004 | 260 | |
| 19 | 2014 | 248 | |
| 20 | 2009 | 242 |
About Fergus J. Couch
Fergus J. Couch is a scholar working on Genetics, Molecular Biology, Cancer Research, Oncology and Pathology and Forensic Medicine, having authored 292 papers that have together received 17.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (144 papers), Cancer Genomics and Diagnostics (66 papers), DNA Repair Mechanisms (50 papers), Genomics and Rare Diseases (37 papers), CRISPR and Genetic Engineering (36 papers), Genetic factors in colorectal cancer (31 papers), Genomic variations and chromosomal abnormalities (23 papers) and Breast Cancer Treatment Studies (23 papers). The work is most often cited by research in Genetics (9.4k citations), Cancer Research (5.0k citations), Oncology (5.4k citations), Pathology and Forensic Medicine (2.8k citations) and Molecular Biology (8.6k citations). Fergus J. Couch has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Sean V. Tavtigian, Katherine L. Nathanson, Álvaro N.A. Monteiro, Barbara L. Weber, Steven N. Hart, James N. Ingle, Kenneth Offit, Judy E. Garber, Douglas F. Easton and Matthew P. Goetz. Their work appears in journals such as Journal of Clinical Oncology, Cancer Research, Breast Cancer Research and Treatment, Cancer Epidemiology Biomarkers & Prevention and Human Mutation.
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.