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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, 2023-11, Vol.24 (1), p.712-712, Article 712

2023

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Increased genetic counseling support improves communication of genetic information in families

Genetics in medicine, 2008-03, Vol.10 (3), p.167-172

2008

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Benefits and burdens of risk management for young people with inherited cancer: A focus on Li-Fraumeni syndrome

Australian journal of general practice, 2021-08, Vol.50 (8), p.538-544

2021

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A national survey of general practitioners' experiences of patient-initiated aggression in Australia

Medical journal of Australia, 2011-06, Vol.194 (11), p.605-608

2011

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Stakeholder perceptions of a nurse led walk-in centre

BMC health services research, 2012-11, Vol.12 (1), p.382-382, Article 382

2012

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Clinically Significant Germline Mutations in Cancer-Causing Genes Identified Through Research Studies Should Be Offered to Research Participants by Genetic Counselors

Journal of clinical oncology, 2016-03, Vol.34 (9), p.898-901

2016

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Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review

European journal of human genetics : EJHG, 2023-01, Vol.31 (1), p.18-34

2023

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"A Natural Progression": Australian Women's Attitudes About an Individualized Breast Screening Model

Cancer prevention research (Philadelphia, Pa.), 2019-06, Vol.12 (6), p.383-390

2019

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The art and science of recruitment to a cancer rapid autopsy programme: A qualitative study exploring patient and clinician experiences

Palliative medicine, 2021-02, Vol.35 (2), p.437-446

2021

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Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes

Journal of genetic counseling, 2023-04, Vol.32 (2), p.495-502

2023

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Exploring Consumers’ Motivations and Experiences of Engaging as Partners in Cancer Research

The patient : patient-centered outcomes research, 2024-07, Vol.17 (4), p.471-479

2024

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Correction: Exploring Consumers’ Motivations and Experiences of Engaging as Partners in Cancer Research

The patient : patient-centered outcomes research, 2024-07, Vol.17 (4), p.481-481

2024

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Development and evaluation of a novel educational program for providers on the use of polygenic risk scores

Genetics in medicine, 2023-08, Vol.25 (8), p.100876-100876, Article 100876

2023

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Reproduction and Genetic Responsibility: An Interpretive Description of Reproductive Decision-Making for Young People With Li-Fraumeni Syndrome

Qualitative health research, 2022-01, Vol.32 (1), p.168-181

2022

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Mainstreaming genomics: training experience of hospital medical officers at the Royal Melbourne Hospital

Internal medicine journal, 2021-02, Vol.51 (2), p.268-271

2021

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Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer

European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1186-1196

2019

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"I need to know if I'm going to die young": Adolescent and young adult experiences of genetic testing for Li-Fraumeni syndrome

Journal of psychosocial oncology, 2021, Vol.39 (1), p.54-73

2021

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Becoming and being a parent with an inherited predisposition to diffuse gastric cancer: A qualitative study of young adults with a CDH1 pathogenic variant

Journal of psychosocial oncology, 2023, Vol.41 (3), p.286-302

2023

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Finding the five‐year window: A qualitative study examining young women's decision‐making and experience of using tamoxifen to reduce BRCA1/2 breast cancer risk

Psycho-oncology (Chichester, England), 2021-02, Vol.30 (2), p.159-166

2021

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Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’

Journal of genetic counseling, 2021-02, Vol.30 (1), p.180-190

2021

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Health professionals’ practice for young people with, or at risk of, Li–Fraumeni syndrome: An Australasian survey

Journal of genetic counseling, 2020-10, Vol.29 (5), p.737-747

2020

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Communicating genetic information in families - a review of guidelines and position papers

European journal of human genetics : EJHG, 2007-06, Vol.15 (6), p.612-618

2007

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Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study

Genetic testing and molecular biomarkers, 2021-12, Vol.25 (12), p.741-748

2021

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Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS)

European journal of human genetics : EJHG, 2015-02, Vol.23 (2), p.152-158

2015

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Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer

Journal of community genetics, 2021-07, Vol.12 (3), p.449-457

2021

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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

Increased genetic counseling support improves communication of genetic information in families

Benefits and burdens of risk management for young people with inherited cancer: A focus on Li-Fraumeni syndrome

A national survey of general practitioners' experiences of patient-initiated aggression in Australia

Stakeholder perceptions of a nurse led walk-in centre

Clinically Significant Germline Mutations in Cancer-Causing Genes Identified Through Research Studies Should Be Offered to Research Participants by Genetic Counselors

Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review

"A Natural Progression": Australian Women's Attitudes About an Individualized Breast Screening Model

The art and science of recruitment to a cancer rapid autopsy programme: A qualitative study exploring patient and clinician experiences

Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes

Exploring Consumers’ Motivations and Experiences of Engaging as Partners in Cancer Research

Correction: Exploring Consumers’ Motivations and Experiences of Engaging as Partners in Cancer Research

Development and evaluation of a novel educational program for providers on the use of polygenic risk scores

Reproduction and Genetic Responsibility: An Interpretive Description of Reproductive Decision-Making for Young People With Li-Fraumeni Syndrome

Mainstreaming genomics: training experience of hospital medical officers at the Royal Melbourne Hospital

Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer

"I need to know if I'm going to die young": Adolescent and young adult experiences of genetic testing for Li-Fraumeni syndrome

Becoming and being a parent with an inherited predisposition to diffuse gastric cancer: A qualitative study of young adults with a CDH1 pathogenic variant

Finding the five‐year window: A qualitative study examining young women's decision‐making and experience of using tamoxifen to reduce BRCA1/2 breast cancer risk

Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’

Health professionals’ practice for young people with, or at risk of, Li–Fraumeni syndrome: An Australasian survey

Communicating genetic information in families - a review of guidelines and position papers

Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study

Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS)

Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer

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