Heidi Howard
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
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- Ethics in Clinical Research
Papers in
- Genetics 39
- BRCA gene mutations in cancer 25
- Genomics and Rare Diseases 16
- Physiology 33
- Biomedical Ethics and Regulation 33
- Co-authors
- Pascal Borry (38 shared papers)Martina C. Cornel (17 shared papers)Emilia Niemiec (15 shared papers)Carla van El (11 shared papers)Bartha Maria Knoppers (5 shared papers)Wybo Dondorp (8 shared papers)Ros Hastings (4 shared papers)Florence Fellmann (3 shared papers)
- Journals
- European Journal of Human Genetics (17 papers)EMBO Reports (3 papers)Genetics in Medicine (2 papers)Nature Reviews Genetics (2 papers)Proceedings of the VLDB Endowment (2 papers)
- Partner nations
- BelgiumSwedenUnited Kingdom
In The Last Decade
Heidi Howard
83 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 142
- Genetics 1.4k
- Public Health, Environmental and Occupational Health 845
- Pediatrics, Perinatology and Child Health 453
- Business and International Management 42
- Physiology 502
Countries citing papers authored by Heidi Howard
This map shows the geographic impact of Heidi Howard'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 Heidi Howard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi Howard more than expected).
Fields of papers citing papers by Heidi Howard
This network shows the impact of papers produced by Heidi Howard. 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 Heidi Howard. The network helps show where Heidi Howard may publish in the future.
Co-authors
The 25 scholars most cited alongside Heidi Howard, 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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 270 |
| 2 | 2013 | 256 | |
| 3 | 2016 | 213 | |
| 4 | 2015 | 98 | |
| 5 | 2010 | 85 | |
| 6 | 2020 | 82 | |
| 7 | 2015 | 81 | |
| 8 | 2012 | 78 | |
| 9 | 2011 | 66 | |
| 10 | 2019 | 65 | |
| 11 | 2003 | 64 | |
| 12 | 2011 | 63 | |
| 13 | 2018 | 60 | |
| 14 | 1998 | 59 | |
| 15 | 2018 | 50 | |
| 16 | 2011 | 50 | |
| 17 | 2017 | 49 | |
| 18 | 2018 | 47 | |
| 19 | 2014 | 43 | |
| 20 | 2009 | 43 |
About Heidi Howard
Heidi Howard is a scholar working on Genetics, Physiology, Public Health, Environmental and Occupational Health, Molecular Biology and Computer Networks and Communications, having authored 88 papers that have together received 2.7k indexed citations. Recurring topics across this work include Biomedical Ethics and Regulation (33 papers), BRCA gene mutations in cancer (25 papers), Ethics in Clinical Research (22 papers), Genomics and Rare Diseases (16 papers), CRISPR and Genetic Engineering (14 papers), Distributed systems and fault tolerance (13 papers), Cloud Computing and Resource Management (7 papers) and Intellectual Property and Patents (6 papers). The work is most often cited by research in Genetics (1.4k citations), Public Health, Environmental and Occupational Health (845 citations), Pediatrics, Perinatology and Child Health (453 citations), Business and International Management (42 citations) and Physiology (502 citations). Heidi Howard has collaborated with scholars based in Belgium, Sweden and United Kingdom. Frequent co-authors include Pascal Borry, Martina C. Cornel, Emilia Niemiec, Carla van El, Bartha Maria Knoppers, Wybo Dondorp, Ros Hastings, Florence Fellmann, Anne Cambon‐Thomsen and Guido M. W. R. de Wert. Their work appears in journals such as European Journal of Human Genetics, EMBO Reports, Genetics in Medicine, Nature Reviews Genetics and Proceedings of the VLDB Endowment.
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.