Kelly E. Ormond

12.9k total citations · 3 hit papers
121 papers, 6.4k citations indexed

About

Kelly E. Ormond is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Kelly E. Ormond has authored 121 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Genetics, 42 papers in Pediatrics, Perinatology and Child Health and 41 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Kelly E. Ormond's work include BRCA gene mutations in cancer (46 papers), Genomics and Rare Diseases (29 papers) and Ethics in Clinical Research (29 papers). Kelly E. Ormond is often cited by papers focused on BRCA gene mutations in cancer (46 papers), Genomics and Rare Diseases (29 papers) and Ethics in Clinical Research (29 papers). Kelly E. Ormond collaborates with scholars based in United States, Switzerland and United Kingdom. Kelly E. Ormond's co-authors include Michael S. Watson, Bruce R. Korf, Sarah S. Kalia, Christa Lese Martin, Jonathan S. Berg, Julianne O’Daniel, Heidi L. Rehm, Marc S. Williams, Wayne W. Grody and Robert C. Green and has published in prestigious journals such as The Lancet, JAMA and SHILAP Revista de lepidopterología.

In The Last Decade

Kelly E. Ormond

115 papers receiving 6.2k citations

Hit Papers

ACMG recommendations for reporting of incidental findings... 2013 2026 2017 2021 2013 2016 2015 500 1000 1.5k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
    2013 1.6k citations Julianne O’Daniel, Kelly E. Ormond et al. profile →
  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
    2016 1.0k citations Kelly E. Ormond et al. profile →
  3. Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
    2015 354 citations Yvonne Bombard, Kelly E. Ormond et al. profile →

Peers

Kelly E. Ormond
Barbara B. Biesecker United States
Anneke Lucassen United Kingdom
Martina C. Cornel Netherlands
Michael S. Watson United States
Pascal Borry Belgium
Robin L. Bennett United States
Mary B. Daly United States
Niels V. Holm Denmark
Jeffrey R. Botkin United States
Caryn Lerman United States
Barbara B. Biesecker United States
Kelly E. Ormond
Citations per year, relative to Kelly E. Ormond Kelly E. Ormond (= 1×) peers Barbara B. Biesecker

Countries citing papers authored by Kelly E. Ormond

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Kelly E. Ormond

This figure shows the co-authorship network connecting the top 25 collaborators of Kelly E. Ormond. A scholar is included among the top collaborators of Kelly E. Ormond based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kelly E. Ormond. Kelly E. Ormond is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Nittas, Vasileios, Kelly E. Ormond, Effy Vayena, & Alessandro Blasimme. (2025). Realizing the promise of machine learning in precision oncology: expert perspectives on opportunities and challenges. BMC Cancer. 25(1). 276–276. 2 indexed citations
2.
Allyse, Megan, Yvonne Bombard, Rosario Isasi, et al.. (2025). Building Better Medicine: Translational Justice and the Quest for Equity in US Healthcare. The American Journal of Bioethics. 25(6). 11–25. 3 indexed citations
3.
McEwen, Alison, et al.. (2025). Developing global consensus about core knowledge and skills for genetic counselor education. Journal of Genetic Counseling. 34(5). e70116–e70116.
4.
Ross, Lainie Friedman & Kelly E. Ormond. (2025). Newborn Sequencing: The Promise and Perils. Annual Review of Genomics and Human Genetics. 26(1). 401–423. 1 indexed citations
5.
Vayena, Effy, et al.. (2024). Experts’ perspectives on human gene editing in Switzerland. Journal of Community Genetics. 16(1). 83–90.
6.
Ormond, Kelly E., et al.. (2024). The global status of genetic counselors in 2023: What has changed in the past 5 years?. SHILAP Revista de lepidopterología. 2(Suppl 2). 101887–101887. 7 indexed citations
7.
Riggan, Kirsten A., Kelly E. Ormond, Megan Allyse, & Sharron Close. (2024). Evidence-based recommendations for delivering the diagnosis of X & Y chromosome multisomies in children, adolescents, and young adults: an integrative review. BMC Pediatrics. 24(1). 263–263. 1 indexed citations
8.
Brall, Caroline, Claudia Berlin, Marcel Zwahlen, et al.. (2022). Public preferences towards data management and governance in Swiss biobanks: results from a nationwide survey. BMJ Open. 12(8). e060844–e060844. 5 indexed citations
9.
10.
Srebniak, Malgorzata I., Attie T. J. I. Go, Lutgarde Govaerts, et al.. (2021). How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies. Clinical Genetics. 100(6). 647–658. 19 indexed citations
11.
Ormond, Kelly E., et al.. (2021). U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients. Journal of Genetic Counseling. 30(6). 1683–1694. 4 indexed citations
12.
Newson, Ainsley J., et al.. (2021). “I wish that there was more info”: characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants. Familial Cancer. 21(2). 143–155. 10 indexed citations
13.
Newson, Ainsley J., et al.. (2019). Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study. Journal of Genetic Counseling. 28(2). 292–303. 10 indexed citations
14.
Buscetta, Ashley, et al.. (2019). Perspectives of Sickle Cell Disease Stakeholders on Heritable Genome Editing. The CRISPR Journal. 2(6). 441–449. 16 indexed citations
15.
Bombard, Yvonne, et al.. (2019). Attitudes of Members of Genetics Professional Societies Toward Human Gene Editing. The CRISPR Journal. 2(5). 331–339. 17 indexed citations
16.
Deuitch, Natalie, et al.. (2019). Attitudes Toward Hypothetical Uses of Gene-Editing Technologies in Parents of People with Autosomal Aneuploidies. The CRISPR Journal. 2(5). 324–330. 17 indexed citations
17.
Schmidlen, Tara, Amy C. Sturm, Shelly R. Hovick, et al.. (2018). Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling. 27(5). 1111–1129. 22 indexed citations
18.
Ormond, Kelly E., Mercy Laurino, Kristine Barlow‐Stewart, et al.. (2018). Genetic counseling globally: Where are we now?. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(1). 98–107. 107 indexed citations
19.
Ormond, Kelly E., Carol Gill, Patrick Semik, & Kristi L. Kirschner. (2003). Attitudes of Health Care Trainees About Genetics and Disability: Issues of Access, Health Care Communication, and Decision Making. Journal of Genetic Counseling. 12(4). 333–349. 29 indexed citations
20.
Kulin, Nathalie A., Anne Pastuszak, Suzanne R. Sage, et al.. (1998). Pregnancy Outcome Following Maternal Use of the New Selective Serotonin Reuptake Inhibitors. Obstetrical & Gynecological Survey. 53(9). 525–526.

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.

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