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Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning

Frontiers in genetics, 2020-03, Vol.11, p.151-151

2020

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Process and outcome in communication of genetic information within families: a systematic review

European journal of human genetics : EJHG, 2007-10, Vol.15 (10), p.999-1011

2007

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Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches

Frontiers in genetics, 2020-08, Vol.11, p.696-696

2020

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Two-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 open, 2023-06, Vol.13 (6), p.e072999-e072999

2023

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Preparing for genomic medicine: a real world demonstration of health system change

Npj genomic medicine, 2017-05, Vol.2 (1), p.16-9, Article 16

2017

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Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery

European journal of human genetics : EJHG, 2022-11, Vol.30 (11), p.1276-1282

2022

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Australian Genomics: A Federated Model for Integrating Genomics into Healthcare

American journal of human genetics, 2019-07, Vol.105 (1), p.7-14

2019

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Making community voices heard in a research-health service alliance, the evolving role of the Community Advisory Group: a case study from the members' perspective

Research involvement and engagement, 2021-11, Vol.7 (1), p.84-12, Article 84

2021

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Parents' experiences of decision making for rapid genomic sequencing in intensive care

European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1804-1810

2021

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Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness

Genetics in medicine, 2019-01, Vol.21 (1), p.173-180

2019

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

Genetics in medicine, 2018-12, Vol.20 (12), p.1554-1563

2018

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Rapid acute care genomics: Challenges and opportunities for genetic counselors

Journal of genetic counseling, 2021-02, Vol.30 (1), p.30-41

2021

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Known unknowns: building an ethics of uncertainty into genomic medicine

BMC medical genomics, 2016-09, Vol.9 (1), p.57-57, Article 57

2016

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Is uptake of genetic testing for colorectal cancer influenced by knowledge of insurance implications?

Medical journal of Australia, 2009-09, Vol.191 (5), p.255-258

2009

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Carrier screening for Beta-thalassaemia: a review of international practice

European journal of human genetics : EJHG, 2010-10, Vol.18 (10), p.1077-1083

2010

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A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1791-1799

2019

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

European journal of human genetics : EJHG, 2019-10, Vol.27 (10), p.1493-1501

2019

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A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability

Genetics in medicine, 2024-10, Vol.26 (10), p.101224, Article 101224

2024

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Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss

Journal of clinical medicine, 2021-12, Vol.11 (1), p.35

2021

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Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness

Genetics in medicine, 2019-02, Vol.21 (2), p.516-516

2019

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Uptake of Offer to Receive Genetic Information about BRCA1 and BRCA2 Mutations in an Australian Population-Based Study

Cancer epidemiology, biomarkers & prevention, 2004-12, Vol.13 (12), p.2258-2263

2004

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Online Prostate Cancer Screening Decision Aid for At-Risk Men: A Randomized Trial

Health psychology, 2014-09, Vol.33 (9), p.986-997

2014

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A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system

Journal of genetic counseling, 2019-04, Vol.28 (2), p.388-397

2019

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How Risk is Perceived, Constructed and Interpreted by Clients in Clinical Genetics, and the Effects on Decision Making: Systematic Review

Journal of genetic counseling, 2008-02, Vol.17 (1), p.30-63

2008

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Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning

Process and outcome in communication of genetic information within families: a systematic review

Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches

Two-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

Preparing for genomic medicine: a real world demonstration of health system change

Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery

Australian Genomics: A Federated Model for Integrating Genomics into Healthcare

Making community voices heard in a research-health service alliance, the evolving role of the Community Advisory Group: a case study from the members' perspective

Parents' experiences of decision making for rapid genomic sequencing in intensive care

Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness

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

Rapid acute care genomics: Challenges and opportunities for genetic counselors

Known unknowns: building an ethics of uncertainty into genomic medicine

Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation

Is uptake of genetic testing for colorectal cancer influenced by knowledge of insurance implications?

Carrier screening for Beta-thalassaemia: a review of international practice

A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

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

A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability

Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss

Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness

Uptake of Offer to Receive Genetic Information about BRCA1 and BRCA2 Mutations in an Australian Population-Based Study

Online Prostate Cancer Screening Decision Aid for At-Risk Men: A Randomized Trial

A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system

How Risk is Perceived, Constructed and Interpreted by Clients in Clinical Genetics, and the Effects on Decision Making: Systematic Review

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