Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
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Title
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-08-11
DOI
10.1038/s41431-022-01168-w
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- Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption
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- Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges
- (2020) Melissa Hill et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Parental experiences of ultrarapid genomic testing for their critically unwell infants and children
- (2020) Gemma R. Brett et al. GENETICS IN MEDICINE
- Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
- (2020) et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children
- (2020) Amanda S. Freed et al. JOURNAL OF PEDIATRICS
- Rapid acute care genomics: Challenges and opportunities for genetic counselors
- (2020) Fiona Lynch et al. Journal of Genetic Counseling
- Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates
- (2019) Samantha Ayres et al. Journal of Genetic Counseling
- Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units
- (2019) Callie J. Diamonstein Journal of Genetic Counseling
- Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges
- (2019) Sarah V. Clowes Candadai et al. Journal of Genetic Counseling
- A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants
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- The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants
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- Parents' experiences of receiving their child's genetic diagnosis: A qualitative study to inform clinical genetics practice
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- What process attributes of clinical genetics services could maximise patient benefits?
- (2008) Marion McAllister et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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