Suzanne E. Hile
Impact in
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
- Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer
Papers in
-
- Genetic factors in colorectal cancer 7
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- DNA Repair Mechanisms 14
- Genomics and Chromatin Dynamics 4
- CRISPR and Genetic Engineering 3
- Co-authors
- Kristin A. Eckert (20 shared papers)Sandeep N. Shah (1 shared paper)Kateryna D. Makova (4 shared papers)Yogeshwar Kelkar (2 shared papers)Francesca Chiaromonte (1 shared paper)Joann Balazs Sweasy (2 shared papers)Ryan P. Barnes (2 shared papers)Marietta Lee (2 shared papers)
- Journals
- Nucleic Acids Research (4 papers)DNA repair (4 papers)Biochemistry (2 papers)Molecular Carcinogenesis (2 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (2 papers)
- Partner nations
- United StatesCzechia
In The Last Decade
Suzanne E. Hile
21 papers receiving 873 citations
Peers
Comparison fields: 5 of 77
- Cancer Research 178
- Pathology and Forensic Medicine 215
- Genetics 264
- Molecular Biology 647
- Oncology 91
Countries citing papers authored by Suzanne E. Hile
This map shows the geographic impact of Suzanne E. Hile'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 Suzanne E. Hile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Suzanne E. Hile more than expected).
Fields of papers citing papers by Suzanne E. Hile
This network shows the impact of papers produced by Suzanne E. Hile. 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 Suzanne E. Hile. The network helps show where Suzanne E. Hile may publish in the future.
Co-authors
The 25 scholars most cited alongside Suzanne E. Hile, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 105 | |
| 2 | 2010 | 96 | |
| 3 | 2009 | 90 | |
| 4 | 2005 | 61 | |
| 5 | 2018 | 58 | |
| 6 | 2003 | 49 | |
| 7 | 2002 | 47 | |
| 8 | 2019 | 45 | |
| 9 | 2012 | 45 | |
| 10 | 2007 | 43 | |
| 11 | 2017 | 43 | |
| 12 | 2011 | 42 | |
| 13 | 2002 | 33 | |
| 14 | Somatic mutation rates and specificities at TC/AG and GT/CA microsatellite sequences in nontumorigenic human lymphoblastoid cells. | 2000 | 29 |
| 15 | 2011 | 26 | |
| 16 | 2014 | 23 | |
| 17 | 2012 | 22 | |
| 18 | 2022 | 15 | |
| 19 | 1998 | 11 | |
| 20 | 2024 | 4 |
About Suzanne E. Hile
Suzanne E. Hile is a scholar working on Pathology and Forensic Medicine, Molecular Biology, Genetics, Cancer Research and Plant Science, having authored 21 papers that have together received 889 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (14 papers), Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), CRISPR and Genetic Engineering (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Cancer Research (178 citations), Pathology and Forensic Medicine (215 citations), Genetics (264 citations), Molecular Biology (647 citations) and Oncology (91 citations). Suzanne E. Hile has collaborated with scholars based in United States and Czechia. Frequent co-authors include Kristin A. Eckert, Sandeep N. Shah, Kateryna D. Makova, Yogeshwar Kelkar, Francesca Chiaromonte, Joann Balazs Sweasy, Ryan P. Barnes, Marietta Lee, Marietta Y. Lee and Guang Yan. Their work appears in journals such as Nucleic Acids Research, DNA repair, Biochemistry, Molecular Carcinogenesis and Mutation research. Fundamental and molecular mechanisms of mutagenesis.
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.