Sharon E. Plon
Impact in
- Genetics top 0.2%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 74
- Genomics and Rare Diseases 41
- BRCA gene mutations in cancer 26
- Genomic variations and chromosomal abnormalities 14
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- DNA Repair Mechanisms 14
- Co-authors
- Murali Chintagumpala (17 shared papers)Heidi L. Rehm (10 shared papers)Jonathan S. Berg (9 shared papers)Debananda Pati (5 shared papers)Mark Groudine (4 shared papers)Rajarshi Ghosh (8 shared papers)James P. Evans (3 shared papers)Carlos D. Bustamante (3 shared papers)
- Journals
- Genetics in Medicine (17 papers)Clinical Cancer Research (13 papers)Human Mutation (10 papers)Pediatric Blood & Cancer (9 papers)The American Journal of Human Genetics (7 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Sharon E. Plon
179 papers receiving 8.8k citations
Sharon E. Plon's Hit Papers
Peers
Comparison fields: 5 of 152
- Genetics 3.3k
- Cancer Research 1.4k
- Pathology and Forensic Medicine 924
- Molecular Biology 3.6k
- Neurology 655
Countries citing papers authored by Sharon E. Plon
This map shows the geographic impact of Sharon E. Plon'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 Sharon E. Plon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sharon E. Plon more than expected).
Fields of papers citing papers by Sharon E. Plon
This network shows the impact of papers produced by Sharon E. Plon. 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 Sharon E. Plon. The network helps show where Sharon E. Plon may publish in the future.
Co-authors
The 25 scholars most cited alongside Sharon E. Plon, 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 191 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ClinGen — The Clinical Genome Resource Hit paper breakdown → | 2015 | 844 |
| 2 | Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Hit paper breakdown → | 2008 | 613 |
| 3 | A brief history of human disease genetics Hit paper breakdown → | 2020 | 379 |
| 4 | 2003 | 249 | |
| 5 | 2001 | 221 | |
| 6 | Abrogation of the G2 checkpoint results in differential radiosensitization of G1 checkpoint-deficient and G1 checkpoint-competent cells. | 1995 | 198 |
| 7 | 2005 | 177 | |
| 8 | 2011 | 174 | |
| 9 | 2007 | 164 | |
| 10 | 2017 | 155 | |
| 11 | 2017 | 143 | |
| 12 | 2017 | 134 | |
| 13 | 2017 | 125 | |
| 14 | 2012 | 123 | |
| 15 | 2007 | 118 | |
| 16 | 2006 | 117 | |
| 17 | 2017 | 115 | |
| 18 | 2012 | 114 | |
| 19 | 2014 | 109 | |
| 20 | 2018 | 100 |
About Sharon E. Plon
Sharon E. Plon is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Oncology, having authored 191 papers that have together received 9.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (41 papers), BRCA gene mutations in cancer (26 papers), Cancer Genomics and Diagnostics (25 papers), Genetic factors in colorectal cancer (24 papers), DNA Repair Mechanisms (14 papers), Neuroblastoma Research and Treatments (14 papers), Genomic variations and chromosomal abnormalities (14 papers) and Childhood Cancer Survivors' Quality of Life (14 papers). The work is most often cited by research in Genetics (3.3k citations), Cancer Research (1.4k citations), Pathology and Forensic Medicine (924 citations), Molecular Biology (3.6k citations) and Neurology (655 citations). Sharon E. Plon has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Murali Chintagumpala, Heidi L. Rehm, Jonathan S. Berg, Debananda Pati, Mark Groudine, Rajarshi Ghosh, James P. Evans, Carlos D. Bustamante, Erin M. Ramos and Sean V. Tavtigian. Their work appears in journals such as Genetics in Medicine, Clinical Cancer Research, Human Mutation, Pediatric Blood & Cancer and The American Journal of Human 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.