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 14
- BRCA gene mutations in cancer 11
- Genomics and Rare Diseases 5
- Nutrition, Genetics, and Disease 3
- Genetic Associations and Epidemiology 3
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- Genetic factors in colorectal cancer 6
- 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)Karen Ouyang (3 shared papers)Brandie Heald (9 shared papers)Swaroop Aradhya (4 shared papers)
- Journals
- Journal of Clinical Oncology (6 papers)JCO Precision Oncology (4 papers)JAMA Network Open (3 papers)Circulation (1 paper)Human Genetics and Genomics Advances (1 paper)
- Partner nations
- United StatesUnited KingdomIsrael
In The Last Decade
Kathryn E. Hatchell
40 papers receiving 453 citations
Kathryn E. Hatchell's Hit Papers
Peers
Comparison fields: 5 of 61
- Genetics 195
- Health Informatics 7
- Pathology and Forensic Medicine 73
- Cancer Research 56
- Cardiology and Cardiovascular Medicine 40
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 | 92 |
| 2 | 2021 | 57 | |
| 3 | 2022 | 40 | |
| 4 | 2022 | 25 | |
| 5 | 2022 | 23 | |
| 6 | 2021 | 22 | |
| 7 | 2021 | 21 | |
| 8 | 2021 | 19 | |
| 9 | 2021 | 17 | |
| 10 | 2022 | 13 | |
| 11 | 2023 | 11 | |
| 12 | 2022 | 10 | |
| 13 | 2021 | 9 | |
| 14 | 2022 | 9 | |
| 15 | 2023 | 9 | |
| 16 | 2019 | 8 | |
| 17 | 2023 | 7 | |
| 18 | 2021 | 6 | |
| 19 | 2019 | 6 | |
| 20 | 2022 | 6 |
About Kathryn E. Hatchell
Kathryn E. Hatchell is a scholar working on Genetics, Pathology and Forensic Medicine, Molecular Biology, Cardiology and Cardiovascular Medicine and Pulmonary and Respiratory Medicine, having authored 40 papers that have together received 456 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (11 papers), Genetic factors in colorectal cancer (6 papers), Genomics and Rare Diseases (5 papers), Renal cell carcinoma treatment (3 papers), Cancer Genomics and Diagnostics (3 papers), Nutrition, Genetics, and Disease (3 papers), Genetic Associations and Epidemiology (3 papers) and Molecular Biology Techniques and Applications (2 papers). The work is most often cited by research in Genetics (195 citations), Health Informatics (7 citations), Pathology and Forensic Medicine (73 citations), Cancer Research (56 citations) and Cardiology and Cardiovascular Medicine (40 citations). Kathryn E. Hatchell has collaborated with scholars based in United States, United Kingdom and Israel. Frequent co-authors include Edward D. Esplin, Robert L. Nussbaum, Sarah M. Nielsen, Susan Rojahn, Britt Johnson, Karen Ouyang, Brandie Heald, Swaroop Aradhya, Shivani Nazareth and Robert Nathan Slotnick. Their work appears in journals such as Journal of Clinical Oncology, JCO Precision Oncology, JAMA Network Open, Circulation and Human Genetics and Genomics Advances.
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.