Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch. Dis. Child. 2018
Times Cited: 2
Times Cited: 2
Times Cited
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Similarity
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Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet. Med. 2017
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Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
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Mainstreaming genetics: a comparative review of clinical services for inherited cardiovascular conditions in the UK.
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Hilary Burton, C Alberg, A Stewart. Public Health Genomics 2010
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Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat. Rev. Genet. 2018
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Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet. Med. 2018
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50
A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
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Emotional distress of mothers of hospitalized children.
J Berenbaum, J Hatcher. J Pediatr Psychol 1992
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Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
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Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
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Sarah V Clowes Candadai, Megan C Sikes, Jenny M Thies, Amanda S Freed, James T Bennett. J Genet Couns 2019
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Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
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Natalie Deuitch, Sandra Soo-Jin Lee, Danton Char. J Genet Couns 2020
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Saskia C Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S Chitty. BMJ Open 2019
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Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
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How infants die in the neonatal intensive care unit: trends from 1999 through 2008.
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Psychological Outcomes in Parents of Critically Ill Hospitalized Children.
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Parents of newborns in the NICU enrolled in genome sequencing research: hopeful, but not naïve.
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Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
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Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
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Deaths in a neonatal intensive care unit: a 10-year perspective.
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Cathrine Monrad Hagen, Thor Willy Ruud Hansen. Pediatr Crit Care Med 2004
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Qualitative data analysis for health services research: developing taxonomy, themes, and theory.
Elizabeth H Bradley, Leslie A Curry, Kelly J Devers. Health Serv Res 2007
Elizabeth H Bradley, Leslie A Curry, Kelly J Devers. Health Serv Res 2007
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Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
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Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
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Potential Psychosocial Risks of Sequencing Newborns.
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Dorothy Brooten, JoAnne M Youngblut, Carmen Caicedo, Lynn Seagrave, G Patricia Cantwell, Balagangadhar Totapally. Am. J. Crit. Care 2016
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Neonatologists' Attitudes About Diagnostic Whole-Genome Sequencing in the NICU.
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Brett Knapp, Carole Decker, John D Lantos. Pediatrics 2019
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Methodological and ethical issues related to qualitative telephone interviews on sensitive topics.
Meredith Mealer, Jacqueline Jones Rn. Nurse Res 2014
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Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU.
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Is there a bias against telephone interviews in qualitative research?
Gina Novick. Res Nurs Health 2008
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Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.
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Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study.
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Rapid Targeted Genomics in Critically Ill Newborns.
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Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease.
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Danton S Char, Sandra Soo-Jin Lee, David Magnus, Mildred Cho. Genet. Med. 2018
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