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K. Ormond · SciRah

Researcher profile · Semantic Scholar

K. Ormond

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K. Ormond — researcher profile on SciRah

h-index: 44
Works: 164
Citations: 12K

Most-cited papers

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
Sarah S. Kalia, Kathy Adelman, S. Bale, W. Chung +13 more
2016Genetics in Medicine1,558 citations Open access
Semantic Scholar
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
J. Botkin, J. Belmont, J. Berg, B. Berkman +8 more
2015American Journal of Human Genetics563 citations Open access
Semantic Scholar
Clinical Interpretation and Implications of Whole-Genome Sequencing
F. Dewey, Megan E. Grove, Cuiping Pan, B. Goldstein +24 more
2014Journal of the American Medical Association (JAMA)454 citations Open access
Semantic Scholar
Improving reporting standards for polygenic scores in risk prediction studies
H. Wand, Samuel A. Lambert, Cecelia P. Tamburro, M. Iacocca +29 more
2020Nature404 citations Open access
Semantic Scholar
The Global State of the Genetic Counseling Profession
M. Abacan, Lamia Alsubaie, K. Barlow-Stewart, Beppy Caanen +34 more
2018European Journal of Human Genetics308 citations Open access
Semantic Scholar
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
W. Dondorp, G. de Wert, Yvonne Bombard, D. Bianchi +18 more
2015European Journal of Human Genetics258 citations Open access
Semantic Scholar
Human Germline Genome Editing.
K. Ormond, D. Mortlock, D. Scholes, Yvonne Bombard +10 more
2017American Journal of Human Genetics239 citations Open access
Semantic Scholar
Beyond Consent: Building Trusting Relationships with Diverse Populations in Precision Medicine Research
S. A. Kraft, M. Cho, Katherine A. Gillespie, M. Halley +5 more
2018American Journal of Bioethics221 citations Open access
Semantic Scholar
Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors
P. Devers, A. Cronister, K. Ormond, Flavia Facio +2 more
2013Journal of Genetic Counseling208 citations Open access
Semantic Scholar
Genetic counseling globally: Where are we now?
K. Ormond, M. Laurino, K. Barlow-Stewart, Tina-Marié Wessels +3 more
2018American Journal of Medical Genetics. Part C, Seminars in Medical Genetics164 citations Open access
Semantic Scholar
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
W. Dondorp, G. de Wert, Yvonne Bombard, D. Bianchi +18 more
2015European Journal of Human Genetics163 citations Open access
Semantic Scholar
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Yvonne Bombard, K. Brothers, S. Fitzgerald-Butt, Nanibaa' A. Garrison +12 more
2019American Journal of Human Genetics114 citations Open access
Semantic Scholar
“I Don’t Want to be Henrietta Lacks”: Diverse Patient Perspectives on Donating Biospecimens for Precision Medicine Research
S. Lee, M. Cho, S. A. Kraft, N. Varsava +4 more
2018Genetics in Medicine95 citations Open access
Semantic Scholar
Expectations and attitudes towards medical artificial intelligence: A qualitative study in the field of stroke
J. Amann, E. Vayena, K. Ormond, D. Frey +2 more
2023PLoS ONE81 citations Open access
Semantic Scholar
Attitudes of Mothers of Children with Down Syndrome Towards Noninvasive Prenatal Testing
G. Kellogg, L. Slattery, L. Hudgins, K. Ormond
2014Journal of Genetic Counseling78 citations Open access
Semantic Scholar
Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures
Alice B. Popejoy, K. Crooks, Stephanie M. Fullerton, L. Hindorff +13 more
2020medRxiv71 citations Open access
Semantic Scholar
Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era
G. Hooker, K. Ormond, K. Sweet, B. Biesecker
2014Journal of Genetic Counseling68 citations Open access
Semantic Scholar
2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling
D. Doyle, Rawan I. Awwad, J. Austin, Bonnie J. Baty +16 more
2016Journal of Genetic Counseling59 citations Open access
Semantic Scholar
Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue
Julia Silver, C. Caleshu, Sylvie Casson-Parkin, K. Ormond
2018Journal of Genetic Counseling57 citations
Semantic Scholar
Public willingness to participate in personalized health research and biobanking: A large-scale Swiss survey
C. Brall, C. Berlin, M. Zwahlen, K. Ormond +2 more
2021PLoS ONE55 citations Open access
Semantic Scholar
Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background
K. Ormond, M. Hallquist, Adam H. Buchanan, Danielle Dondanville +15 more
2018Genetics in Medicine52 citations Open access
Semantic Scholar
Ethical considerations in prenatal testing: Genomic testing and medical uncertainty.
Anastasia Richardson, K. Ormond
2017Seminars in Fetal & Neonatal Medicine52 citations
Semantic Scholar
Best Ethical Practices for Clinicians and Laboratories in the Provision of Non-Invasive Prenatal Testing
MA Allyse, LC Sayres, M. Havard, JS King +7 more
2013Prenatal Diagnosis51 citations Open access
Semantic Scholar
The global status of genetic counselors in 2023: What has changed in the past 5 years?
K. Ormond, Peter James B. Abad, R. MacLeod, Masakazu Nishigaki +1 more
2024Genetics in medicine open50 citations Open access
Semantic Scholar
Translating personalized medicine using new genetic technologies in clinical practice: the ethical issues
K. Ormond, M. Cho
2014Personalized Medicine47 citations Open access
Semantic Scholar
Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives
Kristen Dilzell, K. Kingham, K. Ormond, U. Ladabaum
2014Familial Cancer39 citations
Semantic Scholar
Defining the Critical Components of Informed Consent for Genetic Testing
K. Ormond, Maia J Borensztein, M. Hallquist, A. Buchanan +7 more
2021medRxiv38 citations Open access
Semantic Scholar
The clinical application of gene editing: ethical and social issues.
K. Ormond, Yvonne Bombard, V. Bonham, L. Hoffman-Andrews +6 more
2019Personalized Medicine38 citations
Semantic Scholar
Informed Consent in the Genomics Era.
Shannon Rego, Megan E. Grove, M. Cho, K. Ormond
2020Cold Spring Harbor Perspectives in Medicine37 citations Open access
Semantic Scholar
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: A Framework for the Scalable Delivery of Genomic Counseling and Testing
Tara Schmidlen, A. Sturm, S. Hovick, L. Scheinfeldt +10 more
2018Journal of Genetic Counseling36 citations Open access
Semantic Scholar
Exercise restrictions trigger psychological difficulty in active and athletic adults with hypertrophic cardiomyopathy
Rebecca C. Luiten, K. Ormond, Lisa Post, I. Asif +2 more
2016Open Heart36 citations Open access
Semantic Scholar
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty
Jennifer Hammond, J. E. Klapwijk, M. Hill, Stina Lou +4 more
2020Journal of Genetic Counseling35 citations Open access
Semantic Scholar
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies
J. E. Klapwijk, M. Srebniak, A. Go, L. Govaerts +9 more
2021Clinical Genetics31 citations Open access
Semantic Scholar
Application of a framework to guide genetic testing communication across clinical indications
M. Hallquist, E. Tricou, K. Ormond, J. Savatt +12 more
2021Genome Medicine31 citations Open access
Semantic Scholar
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study
E. Haverfield, E. Esplin, Sienna J. Aguilar, K. Hatchell +21 more
2021BMC Medicine30 citations Open access
Semantic Scholar
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals
C. Lewis, Jennifer Hammond, J. E. Klapwijk, Eleanor Harding +10 more
2021Prenatal Diagnosis30 citations Open access
Semantic Scholar
“Doctors can read about it, they can know about it, but they’ve never lived with it”: How parents use social media throughout the diagnostic odyssey
Natalie T. Deuitch, Erika S. Beckman, M. Halley, Jennifer L Young +6 more
2021Journal of Genetic Counseling30 citations Open access
Semantic Scholar
CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
R. Green, J. Berg, W. Grody, Sarah S. Kalia +10 more
2017Genetics in Medicine27 citations Open access
Semantic Scholar
Exploring the Medical and Psychosocial Concerns of Adolescents and Young Adults With Craniofacial Microsomia
Kayla V Hamilton, K. Ormond, T. Moscarello, Janine S. Bruce +3 more
2018The Cleft Palate-Craniofacial Journal26 citations
Semantic Scholar
Attitudes of people with inherited retinal conditions toward gene editing technology
L. Hoffman-Andrews, R. Mazzoni, Michelle Pacione, Rosemarie Garland-Thomson +1 more
2019Molecular Genetics & Genomic Medicine25 citations Open access
Semantic Scholar
Attitudes of Members of Genetics Professional Societies Toward Human Gene Editing
Alyssa J. Armsby, Yvonne Bombard, Nanibaa' A. Garrison, B. Halpern-Felsher +1 more
2019The CRISPR Journal24 citations Open access
Semantic Scholar
Genetic Counselors’ and Genetic Counseling Students’ Implicit and Explicit Attitudes toward Homosexuality
M. Nathan, K. Ormond, Christopher M. Dial, Amber Gamma +1 more
2019Journal of Genetic Counseling24 citations Open access
Semantic Scholar
Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach
Lauren Puryear, Natalie Downs, A. Nevedal, Eleanor T. Lewis +11 more
2017Journal of Community Genetics24 citations Open access
Semantic Scholar
CORRIGENDUM: 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
Kathy Adelman, S. Bale, W. Chung, C. Eng +14 more
2017Genetics in Medicine24 citations Open access
Semantic Scholar
Building Better Medicine: Translational Justice and the Quest for Equity in US Healthcare
M. Allyse, Preya Agam, Yvonne Bombard, Roel Feys +9 more
2025American Journal of Bioethics23 citations Open access
Semantic Scholar
A genetic counseling needs assessment of Mexico
Daiana Bucio, K. Ormond, Daisy Hernandez, C. Bustamante +1 more
2019Molecular Genetics & Genomic Medicine23 citations Open access
Semantic Scholar
International genetic counseling: What do genetic counselors actually do?
K. Ormond, Laura Hayward, Tina-Marié Wessels, C. Patch +1 more
2023Journal of Genetic Counseling22 citations Open access
Semantic Scholar
Attitudes Toward Hypothetical Uses of Gene-Editing Technologies in Parents of People with Autosomal Aneuploidies
Erika Snure Beckman, Natalie T. Deuitch, Marsha M. Michie, M. Allyse +2 more
2019The CRISPR Journal21 citations
Semantic Scholar
Secondary findings: How did we get here, and where are we going?
K. Ormond, Julianne M. O'Daniel, Sarah S. Kalia
2019Journal of Genetic Counseling20 citations
Semantic Scholar
Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk
K. Broady, K. Ormond, E. Topol, N. J. Schork +1 more
2018Journal of Community Genetics19 citations Open access
Semantic Scholar

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