Ellen Matloff
Impact in
- Genetics top 0.2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 0.5%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 38
- BRCA gene mutations in cancer 37
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
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- Genetic factors in colorectal cancer 5
- Co-authors
- Claudine Isaacs (7 shared papers)D. Gareth Evans (7 shared papers)Henry T. Lynch (7 shared papers)Susan L. Neuhausen (7 shared papers)Timothy R. Rebbeck (6 shared papers)Mary B. Daly (5 shared papers)Olufunmilayo I. Olopade (4 shared papers)Judy E. Garber (3 shared papers)
- Journals
- Journal of Clinical Oncology (6 papers)The Cancer Journal (6 papers)Familial Cancer (2 papers)The Lancet (2 papers)The American Journal of Managed Care (2 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Ellen Matloff
45 papers receiving 4.1k citations
Ellen Matloff's Hit Papers
Peers
Comparison fields: 5 of 90
- Genetics 3.1k
- Reproductive Medicine 837
- Cancer Research 815
- Pathology and Forensic Medicine 727
- Oncology 668
Countries citing papers authored by Ellen Matloff
This map shows the geographic impact of Ellen Matloff'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 Ellen Matloff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ellen Matloff more than expected).
Fields of papers citing papers by Ellen Matloff
This network shows the impact of papers produced by Ellen Matloff. 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 Ellen Matloff. The network helps show where Ellen Matloff may publish in the future.
Co-authors
The 25 scholars most cited alongside Ellen Matloff, 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 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prophylactic Oophorectomy in Carriers ofBRCA1orBRCA2Mutations Hit paper breakdown → | 2002 | 1111 |
| 2 | Bilateral Prophylactic Mastectomy Reduces Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: The PROSE Study Group Hit paper breakdown → | 2004 | 866 |
| 3 | 2008 | 415 | |
| 4 | 2005 | 300 | |
| 5 | 2006 | 231 | |
| 6 | 2002 | 220 | |
| 7 | 2003 | 215 | |
| 8 | 2000 | 90 | |
| 9 | 1999 | 89 | |
| 10 | 2012 | 88 | |
| 11 | Errors in delivery of cancer genetics services: implications for practice. | 2010 | 82 |
| 12 | 2007 | 69 | |
| 13 | 2008 | 56 | |
| 14 | 2010 | 54 | |
| 15 | 2009 | 52 | |
| 16 | 2006 | 45 | |
| 17 | 2019 | 44 | |
| 18 | 2014 | 42 | |
| 19 | Local recurrence in the conservatively treated breast cancer patient: a correlation with age and family history. | 1998 | 35 |
| 20 | 2005 | 26 |
About Ellen Matloff
Ellen Matloff is a scholar working on Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health, Cancer Research and Molecular Biology, having authored 46 papers that have together received 4.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (37 papers), Genomics and Rare Diseases (5 papers), Genetic factors in colorectal cancer (5 papers), Prenatal Screening and Diagnostics (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Biomedical Ethics and Regulation (3 papers) and Ethics in Clinical Research (3 papers). The work is most often cited by research in Genetics (3.1k citations), Reproductive Medicine (837 citations), Cancer Research (815 citations), Pathology and Forensic Medicine (727 citations) and Oncology (668 citations). Ellen Matloff has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Claudine Isaacs, D. Gareth Evans, Henry T. Lynch, Susan L. Neuhausen, Timothy R. Rebbeck, Mary B. Daly, Olufunmilayo I. Olopade, Judy E. Garber, Steven A. Narod and Tara M. Friebel. Their work appears in journals such as Journal of Clinical Oncology, The Cancer Journal, Familial Cancer, The Lancet and The American Journal of Managed Care.
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.