'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health …
H McInnes‐Dean, R Mellis, M Daniel… - Prenatal …, 2024 - Wiley Online Library
Abstract Objectives In October 2020, rapid prenatal exome sequencing (pES) was
introduced into routine National Health Service (NHS) care in England. This study aimed to …
introduced into routine National Health Service (NHS) care in England. This study aimed to …
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US
NN Sahin‐Hodoglugil, BR Lianoglou… - Prenatal …, 2023 - Wiley Online Library
Objective There is increasing evidence supporting the clinical utility of next generation
sequencing for identifying fetal genetic disorders. However, there are limited data on the …
sequencing for identifying fetal genetic disorders. However, there are limited data on the …
[HTML][HTML] Using visual storytelling to share aggregate findings with families participating in clinical genomics research
Purpose Sharing aggregate results with research participants is a widely agreed-upon
ethical obligation; yet, there is little research on communicating study results to diverse …
ethical obligation; yet, there is little research on communicating study results to diverse …
Should incidental findings arising from prenatal testing be reported indiscriminately to patients?
V Kaneva, I Dimitrova - Clinical ethics at the crossroads of genetic and …, 2023 - Elsevier
In this chapter, we focus on the complexity of ethical issues related to reporting incidental
findings from genetic tests in prenatal care and on the main problems that practitioners and …
findings from genetic tests in prenatal care and on the main problems that practitioners and …