Detalhe da pesquisa
1.
How do women talk about self-funded breast cancer genetic testing?: Small stories and stance-taking strategies.
J Genet Couns
; 2023 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37667416
2.
Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes.
J Genet Couns
; 32(2): 495-502, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36480151
3.
Real world outcomes and implementation pathways of exome sequencing in an adult genetic department.
Genet Med
; 24(7): 1536-1544, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35416776
4.
Clinical impact of whole-genome sequencing in patients with early-onset dementia.
J Neurol Neurosurg Psychiatry
; 2022 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35906014
5.
Metaphors and why these are important in all aspects of genetic counseling.
J Genet Couns
; 31(1): 34-40, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233383
6.
Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia.
J Genet Couns
; 31(3): 653-662, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34788484
7.
Genetic testing in dementia-A medical genetics perspective.
Int J Geriatr Psychiatry
; 36(8): 1158-1170, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33779003
8.
Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16.
Int J Mol Sci
; 22(11)2021 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34070858
9.
"It wasn't just for me": Motivations and implications of genetic testing for women at a low risk of hereditary breast and ovarian cancer syndrome.
Psychooncology
; 29(8): 1303-1311, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32497346
10.
Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot study.
J Paediatr Child Health
; 56(8): 1263-1269, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32468641
11.
Consumer attitudes and preferences toward psychiatric genetic counselling and educational resources: A scoping review.
Patient Educ Couns
; 123: 108229, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38461792
12.
Young-onset dementia: A systematic review of the psychological and social impact on relatives.
Patient Educ Couns
; 107: 107585, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36516659
13.
Family Communication about Diagnostic Genetic Testing for Younger-Onset Dementia.
J Pers Med
; 13(4)2023 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37109007
14.
Personalising genetic counselling (POETIC) trial: Protocol for a hybrid type II effectiveness-implementation randomised clinical trial of a patient screening tool to improve patient empowerment after cancer genetic counselling.
Trials
; 24(1): 712, 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37941026
15.
Suicide in frontotemporal dementia and Huntington disease: analysis of family-reported pedigree data and implications for genetic healthcare for asymptomatic relatives.
Psychol Health
; 36(11): 1397-1402, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33232178
16.
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.
J Neurol Sci
; 420: 117260, 2021 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33310205
17.
Cloning, purification and characterisation of brassinin glucosyltransferase, a phytoalexin-detoxifying enzyme from the plant pathogen Sclerotinia sclerotiorum.
Fungal Genet Biol
; 46(2): 201-9, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19041410
18.
Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy.
Psychol Health
; 34(10): 1141-1160, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30931645
19.
Fungi have three tetraspanin families with distinct functions.
BMC Genomics
; 9: 63, 2008 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-18241352
20.
Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy.
Ann Clin Transl Neurol
; 4(5): 318-325, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28491899