| Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing M Allyse, M Michie Trends in biotechnology 31 (8), 439-441, 2013 | 120 | 2013 |
| Noninvasive prenatal genetic testing: current and emerging ethical, legal, and social issues MA Minear, S Alessi, M Allyse, M Michie, S Chandrasekharan Annual review of genomics and human genetics 16, 369-398, 2015 | 104 | 2015 |
| Narrating disability, narrating religious practice: reconciliation and fragile X syndrome M Michie, D Skinner Intellectual and Developmental Disabilities 48 (2), 99-111, 2010 | 65 | 2010 |
| Pregnant women in trials of Covid‐19: a critical time to consider ethical frameworks of inclusion in clinical trials R Farrell, M Michie, R Pope Ethics & human research 42 (4), 17-23, 2020 | 57 | 2020 |
| Research participants' perspectives on genotype-driven research recruitment LM Beskow, EE Namey, RJ Cadigan, T Brazg, J Crouch, GE Henderson, ... Journal of Empirical Research on Human Research Ethics 6 (4), 3-20, 2011 | 45 | 2011 |
| Flexible positions, managed hopes: the promissory bioeconomy of a whole genome sequencing cancer study R Haase, M Michie, D Skinner Social science & medicine 130, 146-153, 2015 | 40 | 2015 |
| Toward an ethically sensitive implementation of noninvasive prenatal screening in the global context J Mozersky, V Ravitsky, R Rapp, M Michie, S Chandrasekharan, M Allyse Hastings Center Report 47 (2), 41-49, 2017 | 39 | 2017 |
| “I think we’ve got too many tests!”: prenatal providers’ reflections on ethical and clinical challenges in the practice integration of cell-free DNA screening BL Gammon, SA Kraft, M Michie, M Allyse Ethics, Medicine and Public Health 2 (3), 334-342, 2016 | 39 | 2016 |
| The meaning of genetic research results: reflections from individuals with and without a known genetic disorder RJ Cadigan, M Michie, G Henderson, AM Davis, LM Beskow Journal of Empirical Research on Human Research Ethics 6 (4), 30-40, 2011 | 38 | 2011 |
| “If I could in a small way help”: motivations for and beliefs about sample donation for genetic research M Michie, G Henderson, J Garrett, G Corbie-Smith Journal of Empirical Research on Human Research Ethics 6 (2), 57-70, 2011 | 38 | 2011 |
| Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations BG Skotko, MA Allyse, K Bajaj, RG Best, S Klugman, M Leach, S Meredith, ... Genetics in Medicine 21 (10), 2285-2292, 2019 | 36 | 2019 |
| What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011 GE Henderson, ET Juengst, NMP King, K Kuczynski, M Michie The Journal of Law, Medicine & Ethics 40 (4), 1008-1024, 2012 | 33 | 2012 |
| The clinical application of gene editing: ethical and social issues KE Ormond, Y Bombard, VL Bonham, L Hoffman-Andrews, H Howard, ... Personalized medicine 16 (4), 337-350, 2019 | 31 | 2019 |
| Spanish-and English-speaking pregnant Women’s views on cfDNA and other prenatal screening: practical and ethical reflections E Floyd, MA Allyse, M Michie Journal of genetic counseling 25, 965-977, 2016 | 31 | 2016 |
| “Don't want no risk and don't want no problems”: public understandings of the risks and benefits of noninvasive prenatal testing in the United States M Allyse, LC Sayres, T Goodspeed, M Michie, MK Cho AJOB empirical bioethics 6 (1), 5-20, 2015 | 24 | 2015 |
| Gene modification therapies: views of parents of people with Down syndrome M Michie, M Allyse Genetics in Medicine 21 (2), 487-492, 2019 | 23 | 2019 |
| “This lifetime commitment”: Public conceptions of disability and noninvasive prenatal genetic screening RJ Steinbach, M Allyse, M Michie, EY Liu, MK Cho American journal of medical genetics Part A 170 (2), 363-374, 2016 | 23 | 2016 |
| Expanding use of cfDNA screening in pregnancy: current and emerging ethical, legal, and social issues L Parham, M Michie, M Allyse Current Genetic Medicine Reports 5, 44-53, 2017 | 21 | 2017 |
| Is preparation a good reason for prenatal genetic testing? Ethical and critical questions M Michie Birth Defects Research 112 (4), 332-338, 2020 | 20 | 2020 |
| What do we do now?: Responding to claims of germline gene editing in humans M Allyse, Y Bombard, R Isasi, M Michie, K Musunuru, KE Ormond Genetics in Medicine 21 (10), 2181-2183, 2019 | 16 | 2019 |
