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1.
Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics).
Genet Med
; 23(7): 1356-1365, 2021 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33824503
2.
The expectations and realities of nutrigenomic testing in australia: A qualitative study.
Health Expect
; 24(2): 670-686, 2021 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33635607
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.
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
J Genet Couns
; 28(2): 367-377, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30779404
5.
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et al.
Genet Med
; 24(5): 1158-1161, 2022 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-35168887
6.
Clinical audit of genetic testing and referral patterns for fragile X and associated conditions.
Am J Med Genet A
; 170(6): 1439-49, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-26892444
7.
Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination.
Reprod Health Matters
; 24(47): 168-77, 2016 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-27578350
8.
'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.
J Paediatr Child Health
; 52(1): 40-6, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26437687
9.
Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.
Aust N Z J Obstet Gynaecol
; 56(6): 605-613, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27402530
10.
Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.
Genet Med
; 16(3): 207-16, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24030436
11.
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
12.
Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing.
Genet Med
; 15(7): 533-40, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23348769
13.
Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.
Twin Res Hum Genet
; 16(2): 601-7, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23331496
14.
What matters to parents? A scoping review of parents' service experiences and needs regarding genetic testing for rare diseases.
Eur J Hum Genet
; 31(8): 869-878, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37308600
15.
Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation.
NPJ Genom Med
; 8(1): 13, 2023 Jun 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-37355653
16.
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
17.
Development and use of the Australian reproductive genetic carrier screening decision aid.
Eur J Hum Genet
; 30(2): 194-202, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34725472
18.
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
J Pers Med
; 12(11)2022 Oct 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-36579509
19.
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
20.
Measuring physician practice, preparedness and preferences for genomic medicine: a national survey.
BMJ Open
; 11(7): e044408, 2021 07 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34244249