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 67
- BRCA gene mutations in cancer 50
- Genomics and Rare Diseases 30
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- Prenatal Screening and Diagnostics 28
- Ethics and Legal Issues in Pediatric Healthcare 19
- Co-authors
- Sarah S. Kalia (4 shared papers)Michael S. Watson (3 shared papers)Bruce R. Korf (4 shared papers)Christa Lese Martin (3 shared papers)Jonathan S. Berg (5 shared papers)Julianne M. O’Daniel (5 shared papers)Heidi L. Rehm (3 shared papers)Amy McGuire (2 shared papers)
- Journals
- Genetics in Medicine (11 papers)The American Journal of Human Genetics (5 papers)Prenatal Diagnosis (5 papers)European Journal of Human Genetics (4 papers)PLoS ONE (4 papers)
- Partner nations
- United StatesSwitzerlandCanada
In The Last Decade
Kelly E. Ormond
139 papers receiving 9.2k citations
Kelly E. Ormond's Hit Papers
Peers
Comparison fields: 5 of 166
- Genetics 4.8k
- Pediatrics, Perinatology and Child Health 1.8k
- Cancer Research 974
- Public Health, Environmental and Occupational Health 1.7k
- Health Informatics 72
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 144 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 | 2018 |
| 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 | 1305 |
| 3 | Clinical assessment incorporating a personal genome Hit paper breakdown → | 2010 | 555 |
| 4 | Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents Hit paper breakdown → | 2015 | 416 |
| 5 | 1998 | 367 | |
| 6 | 2014 | 351 | |
| 7 | Improving reporting standards for polygenic scores in risk prediction studies Hit paper breakdown → | 2021 | 313 |
| 8 | The Global State of the Genetic Counseling Profession Hit paper breakdown → | 2018 | 278 |
| 9 | Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening Hit paper breakdown → | 2015 | 277 |
| 10 | 2010 | 189 | |
| 11 | 2017 | 177 | |
| 12 | 2018 | 169 | |
| 13 | 2013 | 164 | |
| 14 | 2018 | 133 | |
| 15 | 2011 | 119 | |
| 16 | 2011 | 115 | |
| 17 | 2009 | 114 | |
| 18 | 2019 | 94 | |
| 19 | 2003 | 93 | |
| 20 | 2013 | 83 |
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 Physiology, having authored 144 papers that have together received 9.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (50 papers), Genomics and Rare Diseases (30 papers), Prenatal Screening and Diagnostics (28 papers), Ethics in Clinical Research (20 papers), Ethics and Legal Issues in Pediatric Healthcare (19 papers), CRISPR and Genetic Engineering (12 papers), Ethics in medical practice (10 papers) and Biomedical Ethics and Regulation (10 papers). The work is most often cited by research in Genetics (4.8k citations), Pediatrics, Perinatology and Child Health (1.8k citations), Cancer Research (974 citations), Public Health, Environmental and Occupational Health (1.7k citations) and Health Informatics (72 citations). Kelly E. Ormond has collaborated with scholars based in United States, Switzerland and Canada. Frequent co-authors include Sarah S. Kalia, Michael S. Watson, Bruce R. Korf, Christa Lese Martin, Jonathan S. Berg, Julianne M. O’Daniel, Heidi L. Rehm, Amy McGuire, Robert C. Green and Robert Luke Nussbaum. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Prenatal Diagnosis, European Journal of Human Genetics and PLoS ONE.
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.