Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Amy Nisselle
Affiliation
Murdoch Children's Research Institute
ORCID
Career Start Year
2004
Papers
32
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37864047
Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia.
Eur J Hum Genet
2024
37355653
Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation.
NPJ Genom Med
2023
37623006
Workforce Implications of Increased Referrals to Hereditary Cancer Services in Canada: A Scenario-Based Analysis.
Curr Oncol
2023
37943810
An international consensus on effective, inclusive, and career-spanning short-format training in the life sciences and beyond.
PLoS One
2023
34949529
Response to Dwyer et al.
Genet Med
2022
36272999
Co-design, implementation, and evaluation of plain language genomic test reports.
NPJ Genom Med
2022
36353112
Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma.
Front Genet
2022
35953518
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery.
Eur J Hum Genet
2022
33238072
Rapid acute care genomics: Challenges and opportunities for genetic counselors.
J Genet Couns
2021
33635607
The expectations and realities of nutrigenomic testing in australia: A qualitative study.
Health Expect
2021
35072136
GA4GH: International policies and standards for data sharing across genomic research and healthcare.
Cell Genom
2021
34590089
General practitioners' views on genomics, practice and education: A qualitative interview study.
Aust J Gen Pract
2021
34426661
Parents' experiences of decision making for rapid genomic sequencing in intensive care.
Eur J Hum Genet
2021
34244249
Measuring physician practice, preparedness and preferences for genomic medicine: a national survey.
BMJ Open
2021
32194615
Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.
Front Genet
2020
33615052
Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics.
Kidney Int Rep
2020
32194628
Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.
Front Genet
2020
31148592
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
Eur J Hum Genet
2019
31781158
Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic Approach.
Front Genet
2019
31572433
Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.
Front Genet
2019
31569029
Lessons learnt from implementing change in newborn bloodspot screening processes over more than a decade: Midwives, genetics and education.
Midwifery
2019
30779404
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
J Genet Couns
2019
30458892
Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia.
Twin Res Hum Genet
2018
23098241
Why do people choose not to have screening for hemochromatosis?
Genet Test Mol Biomarkers
2013
22194567
Essays on science and society. Lessons from a science education portal.
Science
2011
20583211
HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis.
Hepatology
2010
18199861
Iron-overload-related disease in HFE hereditary hemochromatosis.
N Engl J Med
2008
18697195
Consumer contribution to the delivery of genetic health services.
Am J Med Genet A
2008
18290779
Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload.
Liver Int
2008
16433697
Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosis.
Clin Genet
2006
16039334
Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.
Lancet
2005
15099342
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.
Clin Genet
2004
1 - 32 of 32
Column Actions
Search
Recommended Authors
Kunal Sanghavi
Career Start Year
2012
Number of shared co-authors
1
Leila Jamal
Center for Cancer Research, National Cancer Institute
Career Start Year
2012
Number of shared co-authors
2
Diane M Korngiebel
Google
Career Start Year
2012
Number of shared co-authors
0
Kelly M East
HudsonAlpha Institute for Biotechnology
Career Start Year
2012
Number of shared co-authors
3
Susan E Kelly
University of Exeter
Career Start Year
2009
Number of shared co-authors
2
Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
Career Start Year
2007
Number of shared co-authors
5
Caron Molster
Public Health and Clinical Services Division
Career Start Year
2007
Number of shared co-authors
8
Holly Etchegary
Memorial University
Career Start Year
2006
Number of shared co-authors
3
Pascal Borry
Center for Biomedical Ethics and Law
Career Start Year
2004
Number of shared co-authors
11
Amy L McGuire
Baylor College of Medicine.
Career Start Year
2002
Number of shared co-authors
11
Fiona A Miller
Institute of Health Policy, University of Toronto
Career Start Year
2002
Number of shared co-authors
4
Saskia C Sanderson
University College London
Career Start Year
2001
Number of shared co-authors
3
Holly K Tabor
Stanford Center for Biomedical Ethics (SCBE), Stanford University
Career Start Year
2000
Number of shared co-authors
8
Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
Career Start Year
1999
Number of shared co-authors
6
Alanna Kulchak Rahm
Research Institute
Career Start Year
1997
Number of shared co-authors
3
Lidewij Henneman
location Vrije Universiteit Amsterdam
Career Start Year
1997
Number of shared co-authors
2
Kelly E Ormond
Stanford University School of Medicine
Career Start Year
1996
Number of shared co-authors
6
Sharon Aufox
Northwestern University, Center for Genetic Medicine
Career Start Year
1996
Number of shared co-authors
3
Janet L Williams
Genomic Medicine Institute
Career Start Year
1994
Number of shared co-authors
3
Brenda J Wilson
Memorial University
Career Start Year
1994
Number of shared co-authors
4
Christine Patch
Queen Mary University of London, United Kingdom Society and Ethics Research
Career Start Year
1994
Number of shared co-authors
19
Melanie F Myers
Cincinnati Children's Hospital Medical Center
Career Start Year
1994
Number of shared co-authors
4
William Gregory Feero
Dartmouth Geisel School of Medicine
Career Start Year
1993
Number of shared co-authors
3
Amy A Lemke
Norton Children's Research Institute, University of Louisville School of Medicine
Career Start Year
1992
Number of shared co-authors
1
Anne-Marie Laberge
UNIVERSITY OF MONTREAL
Career Start Year
1991
Number of shared co-authors
2
Wendy R Uhlmann
University of Michigan School of Medicine ann arbor
Career Start Year
1989
Number of shared co-authors
3
Barbara B Biesecker
and Translational Research Center
Career Start Year
1987
Number of shared co-authors
8
June C Carroll
University of Toronto
Career Start Year
1986
Number of shared co-authors
3
Barbara A Bernhardt
Thomas Jefferson University
Career Start Year
1980
Number of shared co-authors
3
Wylie Burke
The Heart Institute, Cincinnati Children's Hospital Medical Center
Career Start Year
1975
Number of shared co-authors
10
row(s) 1 - 30 of 30
Collaborators
Clara Gaff
Murdoch Children's Research Institute
Co-authored papers
16
Zornitza Stark
Murdoch Children's Research Institute
Co-authored papers
7
Robert Williamson
Murdoch Children's Research Institute
Co-authored papers
3
Lawrie W Powell
The University of Queensland
Co-authored papers
3
Anna Middleton
Kavli Centre for Ethics, University of Cambridge
Co-authored papers
2
Ainsley J Newson
Sydney Health Ethics, Sydney School of Public Health, The University of Sydney
Co-authored papers
2
Danya F Vears
University of Melbourne
Co-authored papers
2
Graham G Giles
Co-authored papers
2
Ada Hamosh
Johns Hopkins University School of Medicine
Co-authored papers
1
Jerome Kelleher
University of Oxford
Co-authored papers
1
Angel Pizarro
The Institute for Translational Medicine and Therapeutics, University of Pennsylvania
Co-authored papers
1
Michael J S Beauvais
McGill University
Co-authored papers
1
Soichi Ogishima
Tohoku University Graduate School of Medicine
Co-authored papers
1
Helen Schuilenburg
European Bioinformatics Institute
Co-authored papers
1
Torsten Schwede
University of Basel
Co-authored papers
1
Brian Walsh
Oregon Health & Science University
Co-authored papers
1
Rachele M Hendricks-Sturrup
Duke-Margolis Center for Health Policy
Co-authored papers
1
Monica C Munoz-Torres
University of Colorado Anschutz Medical Campus
Co-authored papers
1
Megan Doerr
Cleveland Clinic
Co-authored papers
1
Neerjah Skantharajah
Ontario Institute for Cancer Research
Co-authored papers
1
Robert M Davies
Wellcome Sanger Institute
Co-authored papers
1
Danielle Denisko
University of Toronto
Co-authored papers
1
Melissa A Haendel
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
Reece K Hart
Broad Institute of MIT and Harvard
Co-authored papers
1
Tristan Nelson
Genomic Medicine Institute
Co-authored papers
1
Debyani Chakravarty
Memorial Sloan Kettering Cancer Center
Co-authored papers
1
Luregn J Schlapbach
and Children's Research Center, University Children's Hospital Zurich
Co-authored papers
1
David Bernick
Broad Institute of MIT and Harvard
Co-authored papers
1
Fiona Cunningham
European Bioinformatics Institute
Co-authored papers
1
Angela Page
Broad Institute
Co-authored papers
1
1 - 30