List of works - Belinda J McClaren

'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.

scientific article published on 10 September 2015

'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening

scientific article published on 05 December 2007

A case for cystic fibrosis carrier testing in the general population

scientific article published on 01 February 2011

A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy

scientific article

A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy

scientific article

Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.

scientific article

Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care

scientific article published on 31 May 2019

Clinical audit of genetic testing and referral patterns for fragile X and associated conditions

scientific article published on 18 February 2016

Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.

scientific article published on 21 January 2013

Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination

scientific article published on 21 May 2016

Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.

scientific article published on 12 July 2016

Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening

scientific article published on 02 October 2017

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.

scientific article

Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making.

scientific article published on 17 November 2011

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.

scientific article published on 12 September 2013

Population-based genetic screening for cystic fibrosis: attitudes and outcomes.

scientific article published on 14 January 2010

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census

scientific article published on 19 February 2019

Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening

scientific article

List of works by Belinda J McClaren

'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.

'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening

A case for cystic fibrosis carrier testing in the general population

A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy

A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy

Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.

Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care

Clinical audit of genetic testing and referral patterns for fragile X and associated conditions

Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.

Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination

Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.

Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.

Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making.

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.

Population-based genetic screening for cystic fibrosis: attitudes and outcomes.

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census

Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening