Heather E. Williams
Impact in
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- Cancer Genomics and Diagnostics
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- Mathematical Biology Tumor Growth
Papers in
- Genetics 7
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 3
- Fetal and Pediatric Neurological Disorders 1
- Co-authors
- Ilana Blum (1 shared paper)Thomas Liehr (4 shared papers)Anja Weise (2 shared papers)Federico A. Monzon (1 shared paper)Anthony W.I. Lo (1 shared paper)Keyur Pravinchandra Patel (1 shared paper)Paweł Mróz (1 shared paper)Timothy J. O’Leary (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)The Journal of Pediatrics (1 paper)Frontiers in Genetics (1 paper)Proceedings of the National Academy of Sciences (1 paper)Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (1 paper)
- Partner nations
- United StatesGermanyPortugal
In The Last Decade
Heather E. Williams
15 papers receiving 391 citations
Heather E. Williams's Hit Papers
Peers
Comparison fields: 5 of 84
- Cancer Research 76
- Modeling and Simulation 19
- Genetics 102
- Genetics 27
- Pathology and Forensic Medicine 43
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 | 169 |
| 2 | 2018 | 65 | |
| 3 | 2021 | 42 | |
| 4 | 2021 | 41 | |
| 5 | 2013 | 34 | |
| 6 | 2022 | 13 | |
| 7 | 2023 | 12 | |
| 8 | 2019 | 12 | |
| 9 | 2021 | 12 | |
| 10 | 2021 | 3 | |
| 11 | 2022 | 3 | |
| 12 | 2023 | 2 | |
| 13 | 2023 | 1 | |
| 14 | 2022 | 1 | |
| 15 | 2022 | 1 |
About Heather E. Williams
Heather E. Williams is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Health Information Management and Modeling and Simulation, having authored 15 papers that have together received 411 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Competitive and Knowledge Intelligence (1 paper), RNA modifications and cancer (1 paper), Gene Regulatory Network Analysis (1 paper), Electronic Health Records Systems (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Cancer Research (76 citations), Modeling and Simulation (19 citations), Genetics (102 citations), Genetics (27 citations) and Pathology and Forensic Medicine (43 citations). Heather E. Williams has collaborated with scholars based in United States, Germany and Portugal. Frequent co-authors include Ilana Blum, Thomas Liehr, Anja Weise, Federico A. Monzon, Anthony W.I. Lo, Keyur Pravinchandra Patel, Paweł Mróz, Timothy J. O’Leary, Mingyang Song and Susan M. Mockus. Their work appears in journals such as Genetics in Medicine, The Journal of Pediatrics, Frontiers in Genetics, Proceedings of the National Academy of Sciences and Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.
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.