Kathryn E. Hatchell
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 21
- BRCA gene mutations in cancer 18
- Genomics and Rare Diseases 10
- Genetic Associations and Epidemiology 4
- Nutrition, Genetics, and Disease 4
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- Genetic factors in colorectal cancer 8
- Co-authors
- Edward D. Esplin (32 shared papers)Robert L. Nussbaum (14 shared papers)Sarah M. Nielsen (24 shared papers)Susan Rojahn (5 shared papers)Britt Johnson (2 shared papers)Brandie Heald (9 shared papers)Karen Ouyang (3 shared papers)Swaroop Aradhya (4 shared papers)
- Journals
- Journal of Clinical Oncology (6 papers)JCO Precision Oncology (4 papers)JAMA Network Open (3 papers)Cancer (1 paper)Familial Cancer (1 paper)
- Partner nations
- United StatesIsraelChile
In The Last Decade
Kathryn E. Hatchell
38 papers receiving 400 citations
Kathryn E. Hatchell's Hit Papers
Peers
Comparison fields: 5 of 66
- Genetics 207
- Health Informatics 9
- Cancer Research 82
- Pathology and Forensic Medicine 79
- Applied Psychology 12
Countries citing papers authored by Kathryn E. Hatchell
This map shows the geographic impact of Kathryn E. Hatchell'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 Kathryn E. Hatchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kathryn E. Hatchell more than expected).
Fields of papers citing papers by Kathryn E. Hatchell
This network shows the impact of papers produced by Kathryn E. Hatchell. 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 Kathryn E. Hatchell. The network helps show where Kathryn E. Hatchell may publish in the future.
Co-authors
The 25 scholars most cited alongside Kathryn E. Hatchell, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing Hit paper breakdown → | 2023 | 78 |
| 2 | 2021 | 47 | |
| 3 | 2022 | 36 | |
| 4 | 2022 | 22 | |
| 5 | 2022 | 21 | |
| 6 | 2021 | 20 | |
| 7 | 2021 | 18 | |
| 8 | 2021 | 17 | |
| 9 | 2021 | 16 | |
| 10 | 2022 | 12 | |
| 11 | 2023 | 9 | |
| 12 | 2022 | 9 | |
| 13 | 2022 | 9 | |
| 14 | 2021 | 9 | |
| 15 | 2023 | 8 | |
| 16 | 2019 | 7 | |
| 17 | 2023 | 6 | |
| 18 | 2022 | 6 | |
| 19 | 2021 | 6 | |
| 20 | 2022 | 5 |
About Kathryn E. Hatchell
Kathryn E. Hatchell is a scholar working on Genetics, Pathology and Forensic Medicine, Molecular Biology, Cancer Research and Oncology, having authored 40 papers that have together received 402 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (18 papers), Genomics and Rare Diseases (10 papers), Genetic factors in colorectal cancer (8 papers), Cancer Genomics and Diagnostics (6 papers), Renal cell carcinoma treatment (4 papers), Genetic Associations and Epidemiology (4 papers), Nutrition, Genetics, and Disease (4 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Genetics (207 citations), Health Informatics (9 citations), Cancer Research (82 citations), Pathology and Forensic Medicine (79 citations) and Applied Psychology (12 citations). Kathryn E. Hatchell has collaborated with scholars based in United States, Israel and Chile. Frequent co-authors include Edward D. Esplin, Robert L. Nussbaum, Sarah M. Nielsen, Susan Rojahn, Britt Johnson, Brandie Heald, Karen Ouyang, Swaroop Aradhya, Robert Nathan Slotnick and Dianalee McKnight. Their work appears in journals such as Journal of Clinical Oncology, JCO Precision Oncology, JAMA Network Open, Cancer and Familial 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.