Kathryn E. Hatchell
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Health Informatics top 10%
- Artificial Intelligence in Healthcare and Education
Papers in
- Genetics 28
- BRCA gene mutations in cancer 19
- Genomics and Rare Diseases 8
- Genetic Associations and Epidemiology 2
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- Genetic factors in colorectal cancer 8
- Vitamin D Research Studies 3
- Co-authors
- Edward D. Esplin (24 shared papers)Susan Rojahn (5 shared papers)Robert Luke Nussbaum (12 shared papers)Sarah M. Nielsen (17 shared papers)Britt A. Johnson (2 shared papers)Karen Ouyang (3 shared papers)Swaroop Aradhya (5 shared papers)Brandie Heald (7 shared papers)
- Journals
- JCO Precision Oncology (4 papers)JAMA Network Open (3 papers)Genetics in Medicine (3 papers)Prostate Cancer and Prostatic Diseases (2 papers)Circulation Genomic and Precision Medicine (2 papers)
- Partner nations
- United StatesIsraelChile
In The Last Decade
Kathryn E. Hatchell
39 papers receiving 815 citations
Kathryn E. Hatchell's Hit Papers
Peers
Comparison fields: 5 of 60
- Genetics 443
- Health Informatics 32
- Pathology and Forensic Medicine 95
- Psychiatry and Mental health 61
- Cardiology and Cardiovascular Medicine 65
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 42 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 | 132 |
| 2 | 2023 | 89 | |
| 3 | 2022 | 68 | |
| 4 | 2021 | 66 | |
| 5 | 2021 | 64 | |
| 6 | 2022 | 58 | |
| 7 | 2018 | 31 | |
| 8 | 2022 | 29 | |
| 9 | 2021 | 27 | |
| 10 | 2021 | 25 | |
| 11 | 2021 | 21 | |
| 12 | 2021 | 21 | |
| 13 | 2022 | 21 | |
| 14 | 2021 | 18 | |
| 15 | 2022 | 18 | |
| 16 | 2023 | 16 | |
| 17 | 2022 | 12 | |
| 18 | 2023 | 12 | |
| 19 | 2023 | 12 | |
| 20 | 2022 | 11 |
About Kathryn E. Hatchell
Kathryn E. Hatchell is a scholar working on Genetics, Pathology and Forensic Medicine, Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 42 papers that have together received 838 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (19 papers), Genetic factors in colorectal cancer (8 papers), Genomics and Rare Diseases (8 papers), Vitamin D Research Studies (3 papers), Cardiac electrophysiology and arrhythmias (3 papers), Epilepsy research and treatment (2 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Associations and Epidemiology (2 papers). The work is most often cited by research in Genetics (443 citations), Health Informatics (32 citations), Pathology and Forensic Medicine (95 citations), Psychiatry and Mental health (61 citations) and Cardiology and Cardiovascular Medicine (65 citations). Kathryn E. Hatchell has collaborated with scholars based in United States, Israel and Chile. Frequent co-authors include Edward D. Esplin, Susan Rojahn, Robert Luke Nussbaum, Sarah M. Nielsen, Britt A. Johnson, Karen Ouyang, Swaroop Aradhya, Brandie Heald, Sulagna C. Saitta and Elaine Y. Chen. Their work appears in journals such as JCO Precision Oncology, JAMA Network Open, Genetics in Medicine, Prostate Cancer and Prostatic Diseases and Circulation Genomic and Precision Medicine.
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.