Kelly E. Ormond
Impact in
- Genetics top 0.2%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare
Papers in
- Genetics 62
- BRCA gene mutations in cancer 46
- Genomics and Rare Diseases 29
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- Prenatal Screening and Diagnostics 26
- Ethics and Legal Issues in Pediatric Healthcare 19
- Co-authors
- Michael S. Watson (3 shared papers)Bruce R. Korf (4 shared papers)Sarah S. Kalia (4 shared papers)Christa Lese Martin (3 shared papers)Jonathan S. Berg (5 shared papers)Julianne O’Daniel (5 shared papers)Heidi L. Rehm (3 shared papers)Leslie G. Biesecker (2 shared papers)
- Journals
- Genetics in Medicine (9 papers)Prenatal Diagnosis (5 papers)The American Journal of Human Genetics (5 papers)PLoS ONE (4 papers)Journal of Genetic Counseling (35 papers)
- Partner nations
- United StatesSwitzerlandUnited Kingdom
In The Last Decade
Kelly E. Ormond
115 papers receiving 6.2k citations
Kelly E. Ormond's Hit Papers
Peers
Comparison fields: 5 of 151
- Genetics 3.6k
- Pediatrics, Perinatology and Child Health 1.6k
- Public Health, Environmental and Occupational Health 1.7k
- Cancer Research 776
- Health Informatics 59
Countries citing papers authored by Kelly E. Ormond
This map shows the geographic impact of Kelly E. Ormond'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 Kelly E. Ormond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kelly E. Ormond more than expected).
Fields of papers citing papers by Kelly E. Ormond
This network shows the impact of papers produced by Kelly E. Ormond. 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 Kelly E. Ormond. The network helps show where Kelly E. Ormond may publish in the future.
Co-authors
The 25 scholars most cited alongside Kelly E. Ormond, 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 121 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Hit paper breakdown → | 2013 | 1643 |
| 2 | Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics Hit paper breakdown → | 2016 | 1023 |
| 3 | Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents Hit paper breakdown → | 2015 | 354 |
| 4 | 1998 | 332 | |
| 5 | 2010 | 164 | |
| 6 | 2013 | 155 | |
| 7 | 2017 | 141 | |
| 8 | 2018 | 140 | |
| 9 | 2011 | 115 | |
| 10 | 2018 | 107 | |
| 11 | 2009 | 105 | |
| 12 | 2003 | 85 | |
| 13 | 2019 | 77 | |
| 14 | 2013 | 73 | |
| 15 | 2014 | 68 | |
| 16 | 2018 | 64 | |
| 17 | 2013 | 56 | |
| 18 | 2013 | 52 | |
| 19 | 2014 | 52 | |
| 20 | 2016 | 52 |
About Kelly E. Ormond
Kelly E. Ormond is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, General Health Professions and Molecular Biology, having authored 121 papers that have together received 6.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (46 papers), Ethics in Clinical Research (29 papers), Genomics and Rare Diseases (29 papers), Prenatal Screening and Diagnostics (26 papers), Ethics and Legal Issues in Pediatric Healthcare (19 papers), Ethics in medical practice (12 papers), Biomedical Ethics and Regulation (12 papers) and CRISPR and Genetic Engineering (11 papers). The work is most often cited by research in Genetics (3.6k citations), Pediatrics, Perinatology and Child Health (1.6k citations), Public Health, Environmental and Occupational Health (1.7k citations), Cancer Research (776 citations) and Health Informatics (59 citations). Kelly E. Ormond has collaborated with scholars based in United States, Switzerland and United Kingdom. Frequent co-authors include Michael S. Watson, Bruce R. Korf, Sarah S. Kalia, Christa Lese Martin, Jonathan S. Berg, Julianne O’Daniel, Heidi L. Rehm, Leslie G. Biesecker, Wayne W. Grody and Robert L. Nussbaum. Their work appears in journals such as Genetics in Medicine, Prenatal Diagnosis, The American Journal of Human Genetics, PLoS ONE and Journal of Genetic Counseling.
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.