Publications by authors named "Belinda McClaren"

26Publications

"It's something I've committed to longer term": The impact of an immersion program for physicians on adoption of genomic medicine.

Patient Educ Couns 2020 Oct 11. Epub 2020 Oct 11.

Murdoch Children's Research Institute, Parkville, Australia; Melbourne Genomics Health Alliance, c/o Walter and Eliza Hall Institute, Parkville, Australia; Department of Paediatrics, University of Melbourne, Parkville, Australia. Electronic address:

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October 2020

Rapid acute care genomics: Challenges and opportunities for genetic counselors.

J Genet Couns 2020 Nov 25. Epub 2020 Nov 25.

Australian Genomics Health Alliance, Melbourne, Vic., Australia.

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November 2020

Which types of conditions should be included in reproductive genetic carrier screening? Views of parents of children with a genetic condition.

Eur J Med Genet 2020 Dec 30;63(12):104075. Epub 2020 Sep 30.

Department of Paediatrics, University of Melbourne, Australia; Victorian Clinical Genetics Services, Australia; Murdoch Children's Research Institute, Australia. Electronic address:

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December 2020

Parental experiences after prenatal diagnosis of fetal abnormality.

Semin Fetal Neonatal Med 2018 04 16;23(2):150-154. Epub 2017 Dec 16.

Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia; Genetics Education and Health Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

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April 2018

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

J Community Genet 2018 Jan 2;9(1):71-80. Epub 2017 Oct 2.

Department of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia.

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January 2018

Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination.

Reprod Health Matters 2016 May 21;24(47):168-77. Epub 2016 May 21.

Project Manager, Genetics Education and Health Research, Murdoch Childrens Research Institute, Parkville, Australia; Senior Lecturer, Department of Paediatrics, University of Melbourne, Parkville, Australia.

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May 2016

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

Am J Med Genet A 2016 06 18;170(6):1439-49. Epub 2016 Feb 18.

Genetics Education and Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.

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June 2016

'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 2016 Jan 10;52(1):40-6. Epub 2015 Sep 10.

Victorian Clinical Genetics Services, The Royal Children's Hospital, Melbourne, Victoria, Australia.

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January 2016

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

Eur J Hum Genet 2015 May 30;23(5):575-80. Epub 2014 Jul 30.

Murdoch Childrens Research Institute, Department of Paediatrics, The University of Melbourne, Parkville, Australia.

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May 2015

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

Eur J Hum Genet 2014 Jul 20;22(7):859-65. Epub 2013 Nov 20.

1] Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, VIC, Australia [2] Department of Medicine, Monash University, Clayton, VIC, Australia [3] Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia [4] Clinical Genetics, Austin Health, Heidelberg, VIC, Australia.

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July 2014

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

Genet Med 2014 Mar 12;16(3):207-16. Epub 2013 Sep 12.

1] Murdoch Childrens Research Institute, Parkville, Victoria, Australia [2] Department of Medicine, Monash University, Clayton, Victoria, Australia [3] Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia [4] Clinical Genetics, Austin Health, Heidelberg, Victoria, Australia.

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March 2014

Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing.

Genet Med 2013 Jul 24;15(7):533-40. Epub 2013 Jan 24.

Genetics Education and Health Research, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.

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July 2013