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Confidentiality With Adolescents in the Medical Setting: What Do Parents Think?

Journal of adolescent health, 2011-10, Vol.49 (4), p.428-430

2011

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Confidential Consultations With Adolescents: An Exploration of Australian Parents’ Perspectives

Journal of adolescent health, 2013-06, Vol.52 (6), p.786-791

2013

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Balancing Parental Involvement With Adolescent Friendly Health Care in Teenagers With Diabetes: Are We Getting It Right?

Journal of adolescent health, 2014-07, Vol.55 (1), p.59-64

2014

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Respecting Adolescents’ Autonomy (as Long as They Make the Right Choice)

Journal of adolescent health, 2010-08, Vol.47 (2), p.113-114

2010

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Visual Storytelling: A Beneficial But Challenging Method for Health Research With Young People

Qualitative health research, 2010-12, Vol.20 (12), p.1677-1688

2010

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“It was the missing piece”: adolescent experiences of predictive genetic testing for adult-onset conditions

Genetics in medicine, 2013-08, Vol.15 (8), p.643-649

2013

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Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments

Journal of medical ethics, 2012-09, Vol.38 (9), p.519-524

2012

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Adolescents with Implantable Cardioverter Defibrillators: A Patient and Parent Perspective

Pacing and clinical electrophysiology, 2012-01, Vol.35 (1), p.62-72

2012

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Breaching Confidentiality with Adolescent Clients: A Survey of Australian Psychologists about the Considerations that Influence Their Decisions

Psychiatry, psychology, and law, 2012-04, Vol.19 (2), p.209-220

2012

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Is my mum going to hear this? Methodological and ethical challenges in qualitative health research with young people

Social science & medicine (1982), 2009-12, Vol.69 (11), p.1691-1699

2009

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"They don't really get heard": A qualitative study of sibling involvement across two forms of family-based treatment for adolescent anorexia nervosa

Eating disorders, 2018-07, Vol.26 (4), p.373-387

2018

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"You're one of us now": Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)

American journal of medical genetics. Part C, Seminars in medical genetics, 2008-02, Vol.148C (1), p.47-55

2008

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Ethical Dilemmas of Confidentiality With Adolescent Clients: Case Studies From Psychologists

Ethics & behavior, 2015-05, Vol.25 (3), p.197-221

2015

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Ethical dilemmas associated with genetic testing: which are most commonly seen and how are they managed?

Genetics in medicine, 2013-05, Vol.15 (5), p.345-353

2013

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"I'm scared of being like mum": The Experience of Adolescents Living in Families with Huntington Disease

Journal of Huntington's disease, 2015-09, Vol.4 (3), p.209-217

2015

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“There’s a Whole Different Way of Working with Adolescents”: Interviews with Australian Genetic Counselors About their Experiences with Adolescent Clients

Journal of genetic counseling, 2013-10, Vol.22 (5), p.674-684

2013

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Tricky teens: are they really tricky or do genetic health professionals simply require more training in adolescent health?

Personalized medicine, 2013-08, Vol.10 (6), p.589-600

2013

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“Should I Send a Condolence Card?” Promoting Emotional Safety in Qualitative Health Research Through Reflexivity and Ethical Mindfulness

Qualitative inquiry, 2013-11, Vol.19 (9), p.652-663

2013

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Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening

Health expectations : an international journal of public participation in health care and health policy, 2015-02, Vol.18 (1), p.69-80

2015

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Adolescents, Risk Behaviour and Confidentiality: When Would Australian Psychologists Breach Confidentiality to Disclose Information to Parents?

Australian psychologist, 2013-12, Vol.48 (6), p.408-419

2013

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“Both Sides of the Wheelchair”: The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors

Journal of genetic counseling, 2015-10, Vol.24 (5), p.732-743

2015

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Refusing to provide a prenatal test: can it ever be ethical?

BMJ (British Medical Journal), 2006-11, Vol.333 (7577), p.1066-1068

International edition, 2006

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An international survey of predictive genetic testing in children for adult onset conditions

Genetics in medicine, 2005-07, Vol.7 (6), p.390-396

2005

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"Holding your breath": Interviews with young people who have undergone predictive genetic testing for Huntington disease

American journal of medical genetics. Part A, 2007-09, Vol.143A (17), p.1984-1989

2007

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The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis

Familial cancer, 2010-03, Vol.9 (1), p.27-35

2010

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Confidentiality With Adolescents in the Medical Setting: What Do Parents Think?

Confidential Consultations With Adolescents: An Exploration of Australian Parents’ Perspectives

Balancing Parental Involvement With Adolescent Friendly Health Care in Teenagers With Diabetes: Are We Getting It Right?

Respecting Adolescents’ Autonomy (as Long as They Make the Right Choice)

Visual Storytelling: A Beneficial But Challenging Method for Health Research With Young People

“It was the missing piece”: adolescent experiences of predictive genetic testing for adult-onset conditions

Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments

Adolescents with Implantable Cardioverter Defibrillators: A Patient and Parent Perspective

Breaching Confidentiality with Adolescent Clients: A Survey of Australian Psychologists about the Considerations that Influence Their Decisions

Is my mum going to hear this? Methodological and ethical challenges in qualitative health research with young people

"They don't really get heard": A qualitative study of sibling involvement across two forms of family-based treatment for adolescent anorexia nervosa

"You're one of us now": Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)

Ethical Dilemmas of Confidentiality With Adolescent Clients: Case Studies From Psychologists

Ethical dilemmas associated with genetic testing: which are most commonly seen and how are they managed?

"I'm scared of being like mum": The Experience of Adolescents Living in Families with Huntington Disease

“There’s a Whole Different Way of Working with Adolescents”: Interviews with Australian Genetic Counselors About their Experiences with Adolescent Clients

Tricky teens: are they really tricky or do genetic health professionals simply require more training in adolescent health?

“Should I Send a Condolence Card?” Promoting Emotional Safety in Qualitative Health Research Through Reflexivity and Ethical Mindfulness

Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening

Adolescents, Risk Behaviour and Confidentiality: When Would Australian Psychologists Breach Confidentiality to Disclose Information to Parents?

“Both Sides of the Wheelchair”: The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors

Refusing to provide a prenatal test: can it ever be ethical?

An international survey of predictive genetic testing in children for adult onset conditions

"Holding your breath": Interviews with young people who have undergone predictive genetic testing for Huntington disease

The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis

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