Harriet E. Feilotter
Impact in
- Cancer Research top 2%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Cancer Genomics and Diagnostics
- Biological Psychiatry top 5%
Papers in
-
- Cancer Genomics and Diagnostics 15
- MicroRNA in disease regulation 10
- Genetics 17
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 7
- Co-authors
- Victor A. Tron (6 shared papers)Xiao Zhang (7 shared papers)David Beach (1 shared paper)Jiamin CHEN (3 shared papers)Lois M. Mulligan (4 shared papers)Charis Eng (2 shared papers)Alexander H. Boag (4 shared papers)Xiaolong Yang (3 shared papers)
- Journals
- Journal of Molecular Diagnostics (7 papers)Clinical Cancer Research (3 papers)American Journal Of Pathology (3 papers)BMC Cancer (3 papers)Journal of Medical Genetics (3 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Harriet E. Feilotter
78 papers receiving 3.9k citations
Harriet E. Feilotter's Hit Papers
Peers
Comparison fields: 5 of 125
- Cancer Research 907
- Biological Psychiatry 90
- Molecular Biology 1.9k
- Oncology 707
- Genetics 641
Countries citing papers authored by Harriet E. Feilotter
This map shows the geographic impact of Harriet E. Feilotter'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 Harriet E. Feilotter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harriet E. Feilotter more than expected).
Fields of papers citing papers by Harriet E. Feilotter
This network shows the impact of papers produced by Harriet E. Feilotter. 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 Harriet E. Feilotter. The network helps show where Harriet E. Feilotter may publish in the future.
Co-authors
The 25 scholars most cited alongside Harriet E. Feilotter, 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 83 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 339 | |
| 2 | Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect. | 1995 | 320 |
| 3 | An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome Hit paper breakdown → | 2020 | 270 |
| 4 | 2010 | 220 | |
| 5 | 1994 | 219 | |
| 6 | 1998 | 187 | |
| 7 | 2017 | 177 | |
| 8 | 2016 | 125 | |
| 9 | 2011 | 115 | |
| 10 | 1999 | 114 | |
| 11 | 2022 | 109 | |
| 12 | 2021 | 104 | |
| 13 | 2008 | 103 | |
| 14 | 2011 | 97 | |
| 15 | 2013 | 92 | |
| 16 | 2017 | 86 | |
| 17 | 1991 | 84 | |
| 18 | 2013 | 78 | |
| 19 | 2012 | 64 | |
| 20 | 2012 | 58 |
About Harriet E. Feilotter
Harriet E. Feilotter is a scholar working on Cancer Research, Genetics, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 83 papers that have together received 4.0k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (15 papers), MicroRNA in disease regulation (10 papers), Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (7 papers), Genetic factors in colorectal cancer (5 papers), Molecular Biology Techniques and Applications (5 papers), Lymphoma Diagnosis and Treatment (5 papers) and Lung Cancer Treatments and Mutations (5 papers). The work is most often cited by research in Cancer Research (907 citations), Biological Psychiatry (90 citations), Molecular Biology (1.9k citations), Oncology (707 citations) and Genetics (641 citations). Harriet E. Feilotter has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Victor A. Tron, Xiao Zhang, David Beach, Jiamin CHEN, Lois M. Mulligan, Charis Eng, Alexander H. Boag, Xiaolong Yang, Paul G. Young and Geneviève C. Paré. Their work appears in journals such as Journal of Molecular Diagnostics, Clinical Cancer Research, American Journal Of Pathology, BMC Cancer and Journal of Medical 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.