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Kelly Ormond
Kelly Ormond
Bioethics Researcher, Health Ethics and Policy Lab, ETH and Adjunct Professor, Stanford University
Verified email at hest.ethz.ch
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Cited by
Cited by
Year
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
RC Green, JS Berg, WW Grody, SS Kalia, BR Korf, CL Martin, AL McGuire, ...
Genetics in medicine 15 (7), 565-574, 2013
27022013
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 …
SS Kalia, K Adelman, SJ Bale, WK Chung, C Eng, JP Evans, GE Herman, ...
Genetics in medicine 19 (2), 249-255, 2017
16942017
Clinical assessment incorporating a personal genome
EA Ashley, AJ Butte, MT Wheeler, R Chen, TE Klein, FE Dewey, ...
The Lancet 375 (9725), 1525-1535, 2010
8032010
Pregnancy outcome following maternal use of the new selective serotonin reuptake inhibitors: a prospective controlled multicenter study
NA Kulin, A Pastuszak, SR Sage, B Schick-Boschetto, G Spivey, ...
Jama 279 (8), 609-610, 1998
6281998
Clinical interpretation and implications of whole-genome sequencing
FE Dewey, ME Grove, C Pan, BA Goldstein, JA Bernstein, H Chaib, ...
Jama 311 (10), 1035-1045, 2014
5142014
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
W Dondorp, G De Wert, Y Bombard, DW Bianchi, C Bergmann, P Borry, ...
European Journal of Human Genetics 23 (11), 1438-1450, 2015
4622015
Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents
JR Botkin, JW Belmont, JS Berg, BE Berkman, Y Bombard, IA Holm, ...
The American Journal of Human Genetics 97 (1), 6-21, 2015
4602015
Improving reporting standards for polygenic scores in risk prediction studies
H Wand, SA Lambert, C Tamburro, MA Iacocca, JW O’Sullivan, C Sillari, ...
Nature 591 (7849), 211-219, 2021
3172021
The global state of the genetic counseling profession
MA Abacan, L Alsubaie, K Barlow-Stewart, B Caanen, C Cordier, ...
European Journal of Human Genetics 27 (2), 183-197, 2019
3022019
Human germline genome editing
KE Ormond, DP Mortlock, DT Scholes, Y Bombard, LC Brody, WA Faucett, ...
The American Journal of Human Genetics 101 (2), 167-176, 2017
2802017
Challenges in the clinical application of whole-genome sequencing
KE Ormond, MT Wheeler, L Hudgins, TE Klein, AJ Butte, RB Altman, ...
The Lancet 375 (9727), 1749-1751, 2010
2732010
Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors
PL Devers, A Cronister, KE Ormond, F Facio, CK Brasington, P Flodman
Journal of genetic counseling 22 (3), 291-295, 2013
2552013
Beyond consent: building trusting relationships with diverse populations in precision medicine research
SA Kraft, MK Cho, K Gillespie, M Halley, N Varsava, KE Ormond, HS Luft, ...
The American Journal of Bioethics 18 (4), 3-20, 2018
2012018
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
FE Dewey, R Chen, SP Cordero, KE Ormond, C Caleshu, KJ Karczewski, ...
PLoS genetics 7 (9), e1002280, 2011
1592011
Genetic counseling globally: Where are we now?
KE Ormond, MY Laurino, K Barlow‐Stewart, TM Wessels, S Macaulay, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2018
1572018
Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake
R Tischler, L Hudgins, YJ Blumenfeld, HT Greely, KE Ormond
Prenatal diagnosis 31 (13), 1292-1299, 2011
1552011
Assessing the understanding of biobank participants
KE Ormond, AL Cirino, IB Helenowski, RL Chisholm, WA Wolf
American journal of medical genetics Part A 149 (2), 188-198, 2009
1502009
The genetic family history as a risk assessment tool in internal medicine
TM Frezzo, WS Rubinstein, D Dunham, KE Ormond
Genetics in Medicine 5 (2), 84-91, 2003
1302003
The responsibility to recontact research participants after reinterpretation of genetic and genomic research results
Y Bombard, KB Brothers, S Fitzgerald-Butt, G Nanibaa’A, L Jamal, ...
The American Journal of Human Genetics 104 (4), 578-595, 2019
1162019
Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine
K Salari, KJ Karczewski, L Hudgins, KE Ormond
PLoS One 8 (7), e68853, 2013
1072013
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