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Author Details

Clara Gaff
Murdoch Children's Research Institute
1990
146
35
PMIDPaper TitleJournal TitlePublished Year
36595590Offering and Returning Secondary Findings in the Context of Exome Sequencing for Hearing Loss: Clinicians' Views and Experiences.AJOB Empir Bioeth2023
37454281What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review.Genet Med2023
37308600What matters to parents? A scoping review of parents' service experiences and needs regarding genetic testing for rare diseases.Eur J Hum Genet2023
37270192Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol.BMJ Open2023
37475088Aligning intuition and theory: a novel approach to identifying the determinants of behaviours necessary to support implementation of evidence into practice.Implement Sci2023
37355653Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation.NPJ Genom Med2023
36868206Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.Am J Hum Genet2023
35181209Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children.Genet Med2022
35442192Structured approaches to implementation of clinical genomics: A scoping review.Genet Med2022
36063280Comparing Survival Outcomes for Advanced Cancer Patients Who Received Complex Genomic Profiling Using a Synthetic Control Arm.Target Oncol2022
35953518Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery.Eur J Hum Genet2022
34949529Response to Dwyer et al.Genet Med2022
32939031Clinical impact of genomic testing in patients with suspected monogenic kidney disease.Genet Med2021
35592835Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation.Wellcome Open Res2021
33672413Investigating the Adoption of Clinical Genomics in Australia. An Implementation Science Case Study.Genes (Basel)2021
33635607The expectations and realities of nutrigenomic testing in australia: A qualitative study.Health Expect2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
35011775Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss.J Clin Med2021
34590089General practitioners' views on genomics, practice and education: A qualitative interview study.Aust J Gen Pract2021
34426661Parents' experiences of decision making for rapid genomic sequencing in intensive care.Eur J Hum Genet2021
34838131Making community voices heard in a research-health service alliance, the evolving role of the Community Advisory Group: a case study from the members' perspective.Res Involv Engagem2021
34805637Cost-Effectiveness of Targeted Exome Analysis as a Diagnostic Test in Glomerular Diseases.Kidney Int Rep2021
34748551Return of individual research results from genomic research: A systematic review of stakeholder perspectives.PLoS One2021
34244249Measuring physician practice, preparedness and preferences for genomic medicine: a national survey.BMJ Open2021
34283896Organizational perspectives on implementing complex health interventions: clinical genomics in Australia.J Health Organ Manag2021
32054657Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.Haematologica2021
33310205The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.J Neurol Sci2021
33214711Evaluating the resource implications of different service delivery models for offering additional genomic findings.Genet Med2021
33268232"It's something I've committed to longer term": The impact of an immersion program for physicians on adoption of genomic medicine.Patient Educ Couns2021
33238072Rapid acute care genomics: Challenges and opportunities for genetic counselors.J Genet Couns2021
33151605Professional regulation for Australasian genetic counselors.J Genet Couns2021
33234441Introducing Edna: A trainee chatbot designed to support communication about additional (secondary) genomic findings.Patient Educ Couns2021
32194615Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.Front Genet2020
31827275Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.Eur J Hum Genet2020
31885332From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing.AJOB Empir Bioeth2020
31974413Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project.Genet Med2020
32773771A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients.Genet Med2020
32849770Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches.Front Genet2020
32398772The leadership behaviors needed to implement clinical genomics at scale: a qualitative study.Genet Med2020
32194628Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.Front Genet2020
29765138Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.Genet Med2019
31781158Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic Approach.Front Genet2019
30158691Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.Genet Med2019
31271757Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.Am J Hum Genet2019
31320747A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis.Eur J Hum Genet2019
31572433Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.Front Genet2019
31569029Lessons learnt from implementing change in newborn bloodspot screening processes over more than a decade: Midwives, genetics and education.Midwifery2019
30842113A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol.BMJ Open2019
30779404Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.J Genet Couns2019
30776170A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.J Genet Couns2019
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June C Carroll
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Barbara A Bernhardt
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Collaborators

Zornitza Stark
Murdoch Children's Research Institute
Co-authored papers 24
Bettina Meiser
Co-authored papers 20
Amy Nisselle
Murdoch Children's Research Institute
Co-authored papers 16
Ainsley J Newson
Sydney Health Ethics, Sydney School of Public Health, The University of Sydney
Co-authored papers 10
Judy Kirk
Co-authored papers 10
Anna Middleton
Kavli Centre for Ethics, University of Cambridge
Co-authored papers 8
David P Hansen
Australian e-Health Research Centre, Royal Brisbane and Women's Hospital
Co-authored papers 6
Danya F Vears
University of Melbourne
Co-authored papers 6
Kathryn N North
Murdoch Children's Research Institute
Co-authored papers 5
Graeme Suthers
University of Adelaide
Co-authored papers 5
Graham G Giles
Co-authored papers 5
Brenda Wilson
University of Ottawa
Co-authored papers 4
Fiona Cunningham
European Bioinformatics Institute
Co-authored papers 3
Tiffany Boughtwood
Murdoch Children's Research Institute
Co-authored papers 3
Heidi L Rehm
The Broad Institute of MIT and Harvard
Co-authored papers 3
Stephanie O M Dyke
Montreal Neurological Institute, McGill University
Co-authored papers 3
Bartha Maria Knoppers
McGill University
Co-authored papers 3
Marcel E Dinger
The University of Sydney
Co-authored papers 3
Andrew H Sinclair
Co-authored papers 3
Megan Doerr
Cleveland Clinic
Co-authored papers 2
Adrian Thorogood
Terry Fox Research Institute.
Co-authored papers 2
Moran N Cabili
Foundation Medicine Inc.
Co-authored papers 2
Maarten J IJzerman
Technical Medical Centre, University of Twente
Co-authored papers 2
Yann Joly
McGill University.
Co-authored papers 2
Anthony J Brookes
University of Leicester
Co-authored papers 2
Kazuto Kato
Osaka University
Co-authored papers 2
Amanda B Spurdle
QIMR Berghofer Medical Research Institute
Co-authored papers 2
Calvin W L Ho
Centre for Medical Ethics and Law, University of Hong Kong
Co-authored papers 2
John Christodoulou
University of Melbourne, The Royal Children's Hospital
Co-authored papers 2
Ingrid E Scheffer
Co-authored papers 2
Release 1.2