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1.
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Am J Hum Genet
; 110(3): 419-426, 2023 03 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36868206
2.
Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Am J Hum Genet
; 105(1): 7-14, 2019 07 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31271757
3.
Rapid acute care genomics: Challenges and opportunities for genetic counselors.
J Genet Couns
; 30(1): 30-41, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33238072
4.
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.
Genet Med
; 21(2): 516, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30158691
5.
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.
Genet Med
; 21(1): 173-180, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29765138
6.
A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.
J Genet Couns
; 28(2): 388-397, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30776170
7.
Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Genet Med
; 20(12): 1554-1563, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-29543227
8.
Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.
BMC Med Genet
; 15: 33, 2014 Mar 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-24628824
9.
Prenatal ß-thalassemia carrier screening in Australia: healthcare professionals' perspectives of clinical practice.
Prenat Diagn
; 34(3): 246-50, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24338659
10.
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
; 13(6): e072999, 2023 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-37270192
11.
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery.
Eur J Hum Genet
; 30(11): 1276-1282, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35953518
12.
Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss.
J Clin Med
; 11(1)2021 Dec 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-35011775
13.
Parents' experiences of decision making for rapid genomic sequencing in intensive care.
Eur J Hum Genet
; 29(12): 1804-1810, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34426661
14.
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.
Res Involv Engagem
; 7(1): 84, 2021 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-34838131
15.
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.
Wellcome Open Res
; 6: 311, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35592835
16.
Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.
Front Genet
; 11: 151, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32194628
17.
Attendance of men at the familial cancer clinic: what they value from the consultation.
Genet Med
; 11(6): 434-40, 2009 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-19346953
18.
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
Eur J Hum Genet
; 27(10): 1493-1501, 2019 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31148592
19.
A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis.
Eur J Hum Genet
; 27(12): 1791-1799, 2019 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-31320747
20.
The beliefs, and reported and intended behaviors of unaffected men in response to their family history of prostate cancer.
Genet Med
; 10(6): 430-8, 2008 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-18496220