Heather E. Williams
Impact in
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- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Glioma Diagnosis and Treatment
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- Cancer Genomics and Diagnostics
Papers in
- Co-authors
- Thomas Liehr (4 shared papers)Anja Weise (2 shared papers)Kenji Fujiyoshi (1 shared paper)Anthony W.I. Lo (1 shared paper)Margaret L. Gulley (1 shared paper)Susan M. Mockus (1 shared paper)Timothy J. O’Leary (1 shared paper)Harriet E. Feilotter (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)Molecular Cytogenetics (1 paper)Frontiers in Genetics (1 paper)Journal of Personalized Medicine (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Heather E. Williams
11 papers receiving 298 citations
Heather E. Williams's Hit Papers
Peers
Comparison fields: 5 of 48
- Genetics 117
- Cancer Research 52
- Health Informatics 7
- Genetics 14
- Pediatrics, Perinatology and Child Health 20
Countries citing papers authored by Heather E. Williams
This map shows the geographic impact of Heather E. Williams'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 Heather E. Williams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heather E. Williams more than expected).
Fields of papers citing papers by Heather E. Williams
This network shows the impact of papers produced by Heather E. Williams. 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 Heather E. Williams. The network helps show where Heather E. Williams may publish in the future.
Co-authors
The 25 scholars most cited alongside Heather E. Williams, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC) Hit paper breakdown → | 2022 | 173 |
| 2 | 2021 | 42 | |
| 3 | 2021 | 42 | |
| 4 | 2022 | 13 | |
| 5 | 2019 | 12 | |
| 6 | 2023 | 12 | |
| 7 | 2021 | 3 | |
| 8 | 2022 | 3 | |
| 9 | 2023 | 2 | |
| 10 | 2022 | 1 | |
| 11 | 2022 | 1 |
About Heather E. Williams
Heather E. Williams is a scholar working on Genetics, Anatomy, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 11 papers that have together received 304 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (2 papers), Telemedicine and Telehealth Implementation (1 paper), Ethics in Clinical Research (1 paper), Clinical Laboratory Practices and Quality Control (1 paper), Biomedical Text Mining and Ontologies (1 paper), Medical and Health Sciences Research (1 paper) and COVID-19 and healthcare impacts (1 paper). The work is most often cited by research in Genetics (117 citations), Cancer Research (52 citations), Health Informatics (7 citations), Genetics (14 citations) and Pediatrics, Perinatology and Child Health (20 citations). Heather E. Williams has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Thomas Liehr, Anja Weise, Kenji Fujiyoshi, Anthony W.I. Lo, Margaret L. Gulley, Susan M. Mockus, Timothy J. O’Leary, Harriet E. Feilotter, Thuy L. Phung and Shuji Ogino. Their work appears in journals such as Genetics in Medicine, Molecular Cytogenetics, Frontiers in Genetics, Journal of Personalized Medicine and European 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.