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 26
- Genomics and Rare Diseases 16
- Nutrition, Genetics, and Disease 6
- Physiology 31
- Biomedical Ethics and Regulation 31
- 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)Journal of Risk Research (2 papers)Human Genetics (2 papers)Nature Reviews Genetics (2 papers)
- Partner nations
- BelgiumSwedenUnited Kingdom
In The Last Decade
Heidi Howard
82 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 137
- Genetics 1.3k
- Public Health, Environmental and Occupational Health 687
- Business and International Management 41
- Pediatrics, Perinatology and Child Health 335
- Physiology 403
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 87 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 | 272 |
| 2 | 2013 | 259 | |
| 3 | 2016 | 215 | |
| 4 | 2015 | 99 | |
| 5 | 2010 | 85 | |
| 6 | 2020 | 83 | |
| 7 | 2015 | 83 | |
| 8 | 2012 | 78 | |
| 9 | 2019 | 66 | |
| 10 | 2011 | 66 | |
| 11 | 2003 | 64 | |
| 12 | 2011 | 63 | |
| 13 | 2018 | 62 | |
| 14 | 2011 | 50 | |
| 15 | 2018 | 50 | |
| 16 | 2018 | 49 | |
| 17 | 2017 | 49 | |
| 18 | 2015 | 45 | |
| 19 | 2014 | 43 | |
| 20 | 2009 | 43 |
About Heidi Howard
Heidi Howard is a scholar working on Genetics, Physiology, Public Health, Environmental and Occupational Health, Computer Networks and Communications and Molecular Biology, having authored 87 papers that have together received 2.7k indexed citations. Recurring topics across this work include Biomedical Ethics and Regulation (31 papers), BRCA gene mutations in cancer (26 papers), Ethics in Clinical Research (22 papers), Genomics and Rare Diseases (16 papers), Distributed systems and fault tolerance (13 papers), CRISPR and Genetic Engineering (13 papers), Cloud Computing and Resource Management (7 papers) and Nutrition, Genetics, and Disease (6 papers). The work is most often cited by research in Genetics (1.3k citations), Public Health, Environmental and Occupational Health (687 citations), Business and International Management (41 citations), Pediatrics, Perinatology and Child Health (335 citations) and Physiology (403 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 Hans Scheffer. Their work appears in journals such as European Journal of Human Genetics, EMBO Reports, Journal of Risk Research, Human Genetics and Nature Reviews 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.