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Allyse, Megan

https://orcid.org/0000-0001-6136-9256

Mayo Clinic

Mayo Clinic

Citations 65

The Clinical Application of Gene Editing: Ethical and Social Issues
Ormond, Kelly E. , Bonham, Vence L. , Hoffman‐Andrews, Lily , Howard, Heidi , Isasi, Rosario , Michie, Marsha , Allyse, Megan , Allyse, Megan A , Bombard, Yvonne , Musunuru, Kiran , Riggan, Kirsten A.

Personalized Medicine | July 23, 2019 | Volume: 16 | Issue: 4 | Pages: 337-350

10.2217/pme-2018-0155 Get It

Ethical considerations of maternal–fetal intervention in a twin pregnancy discordant for anomalies
Riggan, Kirsten A. , Collura, Christopher A. , Pittock, Siobhán T. , Ruano, Rodrigo , Whitford, Kevin J. , Allyse, Megan , Ruano, Rodrigo , Pittock, Siobhan , Allyse, Megan A , Riggan, Kirsten A

The Journal of Maternal-Fetal & Neonatal Medicine | June 13, 2019 | Volume: 34 | Issue: 8 | Pages: 1312-1317

10.1080/14767058.2019.1631793 Get It

Where Will We Draw the Line? Public Opinions of Human Gene Editing
Riggan, Kirsten A. , Sharp, Richard R. , Allyse, Megan , Sharp, Richard R , Allyse, Megan A , Riggan, Kirsten A

Qualitative Health Research | May 6, 2019 | Volume: 29 | Issue: 12 | Pages: 1823-1835

10.1177/1049732319846867 Get It

The application of gene editing technologies to prevent or mitigate genetic disease in humans is considered one of its most promising applications. However, as the technology advances, it is imperative to understand the views of the broader public on how it should be used. We conducted focus groups to understand public views on the ethical permissibility and governance of gene editing technologies in humans. A total of 50 urban and semirural residents in the upper Midwest took part in six focus groups. Participants expressed multiple concerns about nonmedical uses of gene editing and its potential for unknown harms to human health, and were divided as to whether the individual patient or “medical experts” should be charged with overseeing the scope of its application. As potential stakeholders, the perspectives from the general public are critical to assess as genome editing technologies advance toward the clinic.
‘Compassionate transfer’: an alternative option for surplus embryo disposition
Riggan, Kirsten A. , Allyse, Megan , Allyse, Megan A , Riggan, Kirsten A

Human Reproduction | February 26, 2019 | Volume: 34 | Issue: 5 | Pages: 791-794

10.1093/humrep/dez038 Get It

Cell-Free DNA Screening During Pregnancy—Reply
Allyse, Megan , Wick, Myra , Allyse, Megan A

JAMA | January 24, 2019 | Volume: 321 | Issue: 3 | Pages: 309

10.1001/jama.2018.18660 Get It

Delivering the Diagnosis of Sex Chromosome Aneuploidy: Experiences and Preferences of Parents and Individuals
Jaramillo, Carolina, Nyquist, Christina , Riggan, Kirsten A. , Egginton, Jason S. , Allyse, Megan , Egginton, Jason, Phelan, Sean, Allyse, Megan A , Phelan, Sean M. , Riggan, Kirsten A

Clinical Pediatrics | December 5, 2018 | Volume: 58 | Issue: 3 | Pages: 336-342

10.1177/0009922818817310 Get It

Increased prenatal diagnoses of sex chromosome aneuploidies (SCAs) amid limited knowledge of their prognoses heighten the need to understand how families contend with the implications of an SCA. To explore the experiences of parents and individuals who received a genetic diagnosis of an SCA (excluding Turner syndrome), we conducted semistructured qualitative telephone interviews with 43 participants affected by these conditions. Parents (n = 35) and individuals (n = 8) expressed almost unanimous interest in more optimistic portrayals of their condition from their providers, even when the prognosis is uncertain. While some participants reported success in receiving accurate information from their provider and identifying supportive resources, numerous families received outdated or misleading information about their condition and lacked direction in accessing follow-up care and support. Parents desire greater coordination of their child’s medical care and access to care that approaches an SCA holistically. Opportunities remain to improve the diagnosis and care of individuals with SCAs.
Decisional regret in women receiving high risk or inconclusive prenatal cell-free DNA screening results
Gammon, Betsy L., Jaramillo, Carolina, Riggan, Kirsten A. , Allyse, Megan , Allyse, Megan A , Riggan, Kirsten A

The Journal of Maternal-Fetal & Neonatal Medicine | October 1, 2018 | Volume: No volume available | Issue: No issue available | Pages: 1-7

10.1080/14767058.2018.1519541 Get It

Weaponizing Hope: Sources of Hope, Unrealistic Optimism, and Denial
Michie, Marsha , Allyse, Megan , Stoll, Katie , Allyse, Megan A , Master, Zubin

The American Journal of Bioethics | September 20, 2018 | Volume: 18 | Issue: 9 | Pages: 25-27

10.1080/15265161.2018.1498946 Get It

Noninvasive Prenatal Genetic Screening Using Cell-free DNA
Allyse, Megan , Wick, Myra , Allyse, Megan A., Wick, Myra J, Allyse, Megan A

JAMA | July 30, 2018 | Volume: 320 | Issue: 6 | Pages: 591

10.1001/jama.2018.9418 Get It

CRSPR/CAS 9 and Human Therapeutics
Allyse, Megan , Allyse, Megan A

Clinical Chemistry | July 27, 2018 | Volume: 64 | Issue: 8 | Pages: 1266-1267

10.1373/clinchem.2018.289447 Get It