| 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 | 2763 | 2013 |
| 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 | 1752 | 2017 |
| 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 | 811 | 2010 |
| 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 | 629 | 1998 |
| 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 | 527 | 2014 |
| 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 | 477 | 2015 |
| 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 | 476 | 2015 |
| 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 | 355 | 2021 |
| 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 | 336 | 2019 |
| 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 | 293 | 2017 |
| 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 | 274 | 2010 |
| 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 | 257 | 2013 |
| 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 | 212 | 2018 |
| 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 | 175 | 2018 |
| 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 | 160 | 2011 |
| 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 | 159 | 2011 |
| 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 | 153 | 2009 |
| 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 | 132 | 2003 |
| 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 | 121 | 2019 |
| 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 | 108 | 2013 |
Yvonne BombardProfessor & Canada Research Chair, University of Toronto & Li Ka Shing Knowledge Institute of St在 utoronto.ca 的电子邮件经过验证
