Sharon E. Plon
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 140
- Genomics and Rare Diseases 86
- BRCA gene mutations in cancer 43
- Genomic variations and chromosomal abnormalities 11
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- Genetic factors in colorectal cancer 22
- Co-authors
- Heidi L. Rehm (9 shared papers)Murali Chintagumpala (11 shared papers)Jonathan S. Berg (10 shared papers)Rajarshi Ghosh (7 shared papers)Erin M. Ramos (5 shared papers)James P. Evans (3 shared papers)Carlos D. Bustamante (3 shared papers)Robert Luke Nussbaum (2 shared papers)
- Journals
- Genetics in Medicine (27 papers)The American Journal of Human Genetics (18 papers)Clinical Cancer Research (16 papers)Human Mutation (14 papers)Pediatric Blood & Cancer (10 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Sharon E. Plon
247 papers receiving 19.9k citations
Sharon E. Plon's Hit Papers
Peers
Comparison fields: 5 of 147
- Genetics 10.2k
- Cancer Research 1k
- Clinical Biochemistry 320
- Pediatrics, Perinatology and Child Health 828
- Health Informatics 140
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 257 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders Hit paper breakdown → | 2013 | 1578 |
| 2 | Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing Hit paper breakdown → | 2014 | 1115 |
| 3 | ClinGen — The Clinical Genome Resource Hit paper breakdown → | 2015 | 1094 |
| 4 | Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Hit paper breakdown → | 2008 | 742 |
| 5 | Pathogenic Germline Variants in 10,389 Adult Cancers Hit paper breakdown → | 2018 | 617 |
| 6 | Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation Hit paper breakdown → | 2016 | 590 |
| 7 | A brief history of human disease genetics Hit paper breakdown → | 2020 | 457 |
| 8 | Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource Hit paper breakdown → | 2017 | 452 |
| 9 | Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium Hit paper breakdown → | 2016 | 451 |
| 10 | 2016 | 391 | |
| 11 | Use of Exome Sequencing for Infants in Intensive Care Units Hit paper breakdown → | 2017 | 358 |
| 12 | Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria Hit paper breakdown → | 2022 | 319 |
| 13 | 2003 | 267 | |
| 14 | 2013 | 261 | |
| 15 | 2016 | 238 | |
| 16 | 2001 | 227 | |
| 17 | Abrogation of the G2 checkpoint results in differential radiosensitization of G1 checkpoint-deficient and G1 checkpoint-competent cells. | 1995 | 194 |
| 18 | 2017 | 190 | |
| 19 | 2015 | 186 | |
| 20 | 2005 | 182 |
About Sharon E. Plon
Sharon E. Plon is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Public Health, Environmental and Occupational Health and Pediatrics, Perinatology and Child Health, having authored 257 papers that have together received 20.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (86 papers), BRCA gene mutations in cancer (43 papers), Genetic factors in colorectal cancer (22 papers), Acute Lymphoblastic Leukemia research (18 papers), Cancer Genomics and Diagnostics (13 papers), DNA Repair Mechanisms (12 papers), Sarcoma Diagnosis and Treatment (11 papers) and Genomic variations and chromosomal abnormalities (11 papers). The work is most often cited by research in Genetics (10.2k citations), Cancer Research (1k citations), Clinical Biochemistry (320 citations), Pediatrics, Perinatology and Child Health (828 citations) and Health Informatics (140 citations). Sharon E. Plon has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Heidi L. Rehm, Murali Chintagumpala, Jonathan S. Berg, Rajarshi Ghosh, Erin M. Ramos, James P. Evans, Carlos D. Bustamante, Robert Luke Nussbaum, Sean V. Tavtigian and Melissa Landrum. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Clinical Cancer Research, Human Mutation and Pediatric Blood & 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.