Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census

(2019) Amy Nisselle et al.   Journal of Genetic Counseling

Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease

(2018) Danton S Char et al.   GENETICS IN MEDICINE

Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?

(2018) Jan M. Friedman et al.   GENETICS IN MEDICINE

Meeting the challenges of implementing rapid genomic testing in acute pediatric care

(2018) Zornitza Stark et al.   GENETICS IN MEDICINE

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

(2018) Lauge Farnaes et al.   npj Genomic Medicine

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants

(2018) Josh E. Petrikin et al.   npj Genomic Medicine

Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children

(2018) Lamia Mestek-Boukhibar et al.   JOURNAL OF MEDICAL GENETICS

Physician Experiences and Understanding of Genomic Sequencing in Oncology

(2017) Caroline M. Weipert et al.   Journal of Genetic Counseling

Rapid Targeted Genomics in Critically Ill Newborns

(2017) Cleo C. van Diemen et al.   PEDIATRICS

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit

(2016) Hussein Daoud et al.   CANADIAN MEDICAL ASSOCIATION JOURNAL

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

(2016) Zornitza Stark et al.   GENETICS IN MEDICINE

Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing

(2016) Michelle J. Bayefsky et al.   PRENATAL DIAGNOSIS

The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing

(2015) Rivka Sukenik-Halevy et al.   GENETICS IN MEDICINE

Rapid whole genome sequencing and precision neonatology

(2015) Joshua E. Petrikin et al.   SEMINARS IN PERINATOLOGY

Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders

(2015) Laurie D. Smith et al.   Cold Spring Harbor Perspectives in Medicine

Emergency medical genomes: a breakthrough application of precision medicine

(2015) Stephen F. Kingsmore et al.   Genome Medicine

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

(2015) Laurel K Willig et al.   Lancet Respiratory Medicine

Organizational readiness for implementing change: a psychometric assessment of a new measure

(2014) Christopher M Shea et al.   Implementation Science

Physicians' Attitudes About Multiplex Tumor Genomic Testing

(2014) Stacy W. Gray et al.   JOURNAL OF CLINICAL ONCOLOGY

Physicians' Preparedness for Integration of Genomic and Pharmacogenetic Testing into Practice Within a Major Healthcare System

(2013) Christina G. Selkirk et al.   Genetic Testing and Molecular Biomarkers

Oncologists’ attitudes toward KRAS testing: a multisite study

(2013) Julie N. Harris et al.   Cancer Medicine

Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine

(2011) K. Bonter et al.   BMJ Open

Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science

(2009) Laura J Damschroder et al.   Implementation Science