Jill E. Stopfer
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Co-authors
- Susan M. Domchek (33 shared papers)Timothy Richard Rebbeck (6 shared papers)Katherine Nathanson (14 shared papers)Judy Ellen Garber (9 shared papers)Barbara L. Weber (4 shared papers)Katrina Armstrong (7 shared papers)Chanita Hughes Halbert (11 shared papers)Barbara Weber (5 shared papers)
- Journals
- Genetics in Medicine (6 papers)Journal of Clinical Oncology (5 papers)Cancer Research (3 papers)Breast Cancer Research and Treatment (3 papers)Familial Cancer (3 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Jill E. Stopfer
73 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 125
- Genetics 2.5k
- Cancer Research 450
- Pathology and Forensic Medicine 460
- Reproductive Medicine 175
- Oncology 542
Countries citing papers authored by Jill E. Stopfer
This map shows the geographic impact of Jill E. Stopfer'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 Jill E. Stopfer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jill E. Stopfer more than expected).
Fields of papers citing papers by Jill E. Stopfer
This network shows the impact of papers produced by Jill E. Stopfer. 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 Jill E. Stopfer. The network helps show where Jill E. Stopfer may publish in the future.
Co-authors
The 25 scholars most cited alongside Jill E. Stopfer, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 562 | |
| 2 | 2004 | 203 | |
| 3 | 2003 | 152 | |
| 4 | 2017 | 144 | |
| 5 | 2008 | 139 | |
| 6 | 2014 | 129 | |
| 7 | 2000 | 128 | |
| 8 | Factors associated with decisions about clinical BRCA1/2 testing. | 2000 | 115 |
| 9 | 2012 | 114 | |
| 10 | 2008 | 91 | |
| 11 | 2016 | 87 | |
| 12 | 2014 | 73 | |
| 13 | 2021 | 67 | |
| 14 | 2006 | 66 | |
| 15 | 2011 | 60 | |
| 16 | 2015 | 57 | |
| 17 | Role of the genetic counselor in familial cancer. | 1996 | 56 |
| 18 | 2011 | 52 | |
| 19 | 2006 | 51 | |
| 20 | 2012 | 46 |
About Jill E. Stopfer
Jill E. Stopfer is a scholar working on Genetics, Oncology, Pediatrics, Perinatology and Child Health, Reproductive Medicine and Pathology and Forensic Medicine, having authored 74 papers that have together received 3.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (61 papers), Ethics in Clinical Research (7 papers), Genetic factors in colorectal cancer (7 papers), Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Cancer Genomics and Diagnostics (5 papers), Ovarian cancer diagnosis and treatment (4 papers) and Cancer Risks and Factors (4 papers). The work is most often cited by research in Genetics (2.5k citations), Cancer Research (450 citations), Pathology and Forensic Medicine (460 citations), Reproductive Medicine (175 citations) and Oncology (542 citations). Jill E. Stopfer has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Susan M. Domchek, Timothy Richard Rebbeck, Katherine Nathanson, Judy Ellen Garber, Barbara L. Weber, Katrina Armstrong, Chanita Hughes Halbert, Barbara Weber, Fergus J. Couch and M. Anne Blackwood. Their work appears in journals such as Genetics in Medicine, Journal of Clinical Oncology, Cancer Research, Breast Cancer Research and Treatment and Familial Cancer.
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.