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Author Details

Amy Nisselle
Murdoch Children's Research Institute
2004
32
13
PMIDPaper TitleJournal TitlePublished Year
37864047Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia.Eur J Hum Genet2024
37355653Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation.NPJ Genom Med2023
37623006Workforce Implications of Increased Referrals to Hereditary Cancer Services in Canada: A Scenario-Based Analysis.Curr Oncol2023
37943810An international consensus on effective, inclusive, and career-spanning short-format training in the life sciences and beyond.PLoS One2023
34949529Response to Dwyer et al.Genet Med2022
36272999Co-design, implementation, and evaluation of plain language genomic test reports.NPJ Genom Med2022
36353112Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma.Front Genet2022
35953518Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery.Eur J Hum Genet2022
33238072Rapid acute care genomics: Challenges and opportunities for genetic counselors.J Genet Couns2021
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
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
34244249Measuring physician practice, preparedness and preferences for genomic medicine: a national survey.BMJ Open2021
32194615Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.Front Genet2020
33615052Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics.Kidney Int Rep2020
32194628Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.Front Genet2020
31148592Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.Eur J Hum Genet2019
31781158Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic Approach.Front 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
30779404Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.J Genet Couns2019
30458892Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia.Twin Res Hum Genet2018
23098241Why do people choose not to have screening for hemochromatosis?Genet Test Mol Biomarkers2013
22194567Essays on science and society. Lessons from a science education portal.Science2011
20583211HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis.Hepatology2010
18199861Iron-overload-related disease in HFE hereditary hemochromatosis.N Engl J Med2008
18697195Consumer contribution to the delivery of genetic health services.Am J Med Genet A2008
18290779Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload.Liver Int2008
16433697Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosis.Clin Genet2006
16039334Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.Lancet2005
15099342Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.Clin Genet2004
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Collaborators

Murdoch Children's Research Institute
Co-authored papers 16
Murdoch Children's Research Institute
Co-authored papers 7
Murdoch Children's Research Institute
Co-authored papers 3
The University of Queensland
Co-authored papers 3
Kavli Centre for Ethics, University of Cambridge
Co-authored papers 2
Sydney Health Ethics, Sydney School of Public Health, The University of Sydney
Co-authored papers 2
University of Melbourne
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Johns Hopkins University School of Medicine
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University of Oxford
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The Institute for Translational Medicine and Therapeutics, University of Pennsylvania
Co-authored papers 1
McGill University
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Tohoku University Graduate School of Medicine
Co-authored papers 1
European Bioinformatics Institute
Co-authored papers 1
University of Basel
Co-authored papers 1
Oregon Health & Science University
Co-authored papers 1
Duke-Margolis Center for Health Policy
Co-authored papers 1
University of Colorado Anschutz Medical Campus
Co-authored papers 1
Cleveland Clinic
Co-authored papers 1
Ontario Institute for Cancer Research
Co-authored papers 1
Wellcome Sanger Institute
Co-authored papers 1
University of Toronto
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
Broad Institute of MIT and Harvard
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Genomic Medicine Institute
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Memorial Sloan Kettering Cancer Center
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and Children's Research Center, University Children's Hospital Zurich
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