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B. McClaren · SciRah

Researcher profile · Semantic Scholar

B. McClaren

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B. McClaren — researcher profile on SciRah

h-index: 23
Works: 52
Citations: 1,368

Most-cited papers

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research
L. Ioannou, B. McClaren, J. Massie, S. Lewis +3 more
2013Genetics in Medicine83 citations Open access
Semantic Scholar
Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning
B. McClaren, Erin Crellin, Monika Janinski, A. Nisselle +3 more
2020Frontiers in Genetics78 citations Open access
Semantic Scholar
Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: A qualitative study
J. Hodgson, Penelope Pitt, S. Metcalfe, J. Halliday +5 more
2016Australian and New Zealand journal of obstetrics and gynaecology76 citations Open access
Semantic Scholar
Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy
Erin Crellin, B. McClaren, A. Nisselle, S. Best +2 more
2019Frontiers in Genetics70 citations Open access
Semantic Scholar
Parental experiences after prenatal diagnosis of fetal abnormality.
J. Hodgson, B. McClaren
2017Seminars in Fetal & Neonatal Medicine62 citations
Semantic Scholar
Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics
K. Jayasinghe, C. Quinlan, A. Mallett, P. Kerr +7 more
2020Kidney International Reports60 citations Open access
Semantic Scholar
‘It is not in my world’: an exploration of attitudes and influences associated with cystic fibrosis carrier screening
B. McClaren, M. Delatycki, V. Collins, S. Metcalfe +1 more
2008European Journal of Human Genetics57 citations
Semantic Scholar
Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
A. Nisselle, Emily King, B. McClaren, Monika Janinski +3 more
2021BMJ Open55 citations Open access
Semantic Scholar
A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy
S. Wong, B. McClaren, A. Archibald, A. Weeks +4 more
2015European Journal of Human Genetics55 citations Open access
Semantic Scholar
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie’s Mission): Design and Implementation
A. Archibald, B. McClaren, J. Caruana, E. Tutty +41 more
2022Journal of Personalized Medicine51 citations Open access
Semantic Scholar
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census
A. Nisselle, I. Macciocca, Fiona McKenzie, Hannah Vuong +4 more
2019Journal of Genetic Counseling46 citations
Semantic Scholar
Nationwide, Couple-Based Genetic Carrier Screening.
Edwin P. Kirk, M. Delatycki, Alison D. Archibald, E. Tutty +77 more
2024New England Journal of Medicine42 citations Open access
Semantic Scholar
Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)
A. Nisselle, Monika Janinski, M. Martyn, B. McClaren +39 more
2021Genetics in Medicine42 citations Open access
Semantic Scholar
A mixed methods exploration of families’ experiences of the diagnosis of childhood spinal muscular atrophy
S. Lawton, C. Hickerton, A. Archibald, B. McClaren +1 more
2014European Journal of Human Genetics41 citations Open access
Semantic Scholar
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
Zornitza Stark, A. Nisselle, B. McClaren, Fiona Lynch +11 more
2019European Journal of Human Genetics38 citations Open access
Semantic Scholar
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
S. Best, H. Brown, S. Lunke, C. Patel +8 more
2021npj Genomic Medicine35 citations Open access
Semantic Scholar
Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening
B. McClaren, S. Metcalfe, Maryanne Aitken, R. Massie +2 more
2010European Journal of Human Genetics35 citations Open access
Semantic Scholar
Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education
B. McClaren, Emily King, Erin Crellin, C. Gaff +2 more
2020Frontiers in Genetics33 citations Open access
Semantic Scholar
Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
J. Hodgson, S. Metcalfe, Maryanne Aitken, S. Donath +7 more
2014BMC Medical Genetics30 citations Open access
Semantic Scholar
Population-Based Genetic Screening for Cystic Fibrosis: Attitudes and Outcomes
L. Ioannou, J. Massie, Veronica Collins, B. McClaren +1 more
2010Public Health Genomics30 citations
Semantic Scholar
Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation
A. Nisselle, Emily King, B. Terrill, B. Davey +5 more
2023npj Genomic Medicine24 citations Open access
Semantic Scholar
Current Practice and Attitudes of Australian Obstetricians Toward Population-Based Carrier Screening for Inherited Conditions
Zornitza Stark, J. Massie, B. McClaren, L. Ioannou +4 more
2013Twin Research and Human Genetics24 citations Open access
Semantic Scholar
Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing
B. McClaren, Maryanne Aitken, J. Massie, D. Amor +2 more
2013Genetics in Medicine23 citations Open access
Semantic Scholar
Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making
A. Archibald, B. McClaren
2011Journal of Community Genetics23 citations Open access
Semantic Scholar
Development and use of the Australian reproductive genetic carrier screening decision aid
Emily King, J. Halliday, A. Archibald, M. Delatycki +3 more
2021European Journal of Human Genetics22 citations Open access
Semantic Scholar
Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination
Penelope Pitt, B. McClaren, J. Hodgson
2016Reproductive Health Matters22 citations Open access
Semantic Scholar
Parents’ experiences of decision making for rapid genomic sequencing in intensive care
Fiona Lynch, A. Nisselle, Zornitza Stark, C. Gaff +1 more
2021European Journal of Human Genetics21 citations Open access
Semantic Scholar
Which types of conditions should be included in reproductive genetic carrier screening?: Views of parents of children with a genetic condition.
L. Thomas, S. Lewis, J. Massie, E. Kirk +6 more
2020European Journal of Medical Genetics21 citations Open access
Semantic Scholar
What matters to parents? A scoping review of parents’ service experiences and needs regarding genetic testing for rare diseases
Erin Crellin, M. Martyn, B. McClaren, C. Gaff
2023European Journal of Human Genetics19 citations Open access
Semantic Scholar
Rapid acute care genomics: Challenges and opportunities for genetic counselors
Fiona Lynch, A. Nisselle, Clara L. Gaff, B. McClaren
2020Journal of Genetic Counseling19 citations
Semantic Scholar
Becoming agents for genomic change: genetic counsellors’ views of patient care and implementation influences when genomics is mainstreamed
T. Do, M. Martyn, B. McClaren, A. McEwen +1 more
2024European Journal of Human Genetics18 citations Open access
Semantic Scholar
General practitioners' views on genomics, practice and education: A qualitative interview study.
M. Cusack, C. Hickerton, A. Nisselle, B. McClaren +4 more
2021Australian Journal of General Practice15 citations Open access
Semantic Scholar
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et al.
S. Righetti, L. Dive, A. Archibald, Lucinda Freeman +6 more
2022Genetics in Medicine14 citations Open access
Semantic Scholar
How do women at increased, but unexplained, familial risk of breast cancer perceive and manage their risk? A qualitative interview study
L. Keogh, B. McClaren, C. Apicella, J. Hopper
2011Hereditary Cancer in Clinical Practice12 citations Open access
Semantic Scholar
"It's something I've committed to longer term": The impact of an immersion program for physicians on adoption of genomic medicine.
M. Martyn, B. McClaren, Monika Janinski, E. Lynch +2 more
2020Patient Education and Counseling11 citations
Semantic Scholar
How do individuals decide whether to accept or decline an offer of genetic testing for colorectal cancer?
L. Keogh, B. McClaren, J. Maskiell, Heather Niven +5 more
2011Hereditary Cancer in Clinical Practice11 citations Open access
Semantic Scholar
Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening
Anita Gorrie, A. Archibald, L. Ioannou, L. Curnow +1 more
2017Journal of Community Genetics10 citations Open access
Semantic Scholar
Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening
L. Ioannou, J. Massie, S. Lewis, V. Collins +2 more
2013European Journal of Human Genetics9 citations Open access
Semantic Scholar
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
Fiona Lynch, A. Nisselle, Zornitza Stark, C. Gaff +1 more
2022European Journal of Human Genetics8 citations Open access
Semantic Scholar
A national education program for rapid genomics in pediatric acute care: building workforce confidence, competence and capability.
Giulia McCorkell, A. Nisselle, Donna Halton, Sophie E. Bouffler +15 more
2024Genetics in Medicine7 citations Open access
Semantic Scholar
Unearthing the Learning of Genomic Medicine in the Workplace: a Qualitative Study
Alice Kim, A. Nisselle, Jennifer M. Weller-Newton, B. McClaren +1 more
2022Vocations and Learning7 citations Open access
Semantic Scholar
The expectations and realities of nutrigenomic testing in australia: A qualitative study
E. Tutty, C. Hickerton, B. Terrill, B. McClaren +10 more
2021Health Expectations7 citations Open access
Semantic Scholar
Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening
Anita Gorrie, A. Archibald, L. Ioannou, L. Curnow +1 more
2017Journal of Community Genetics3 citations Open access
Semantic Scholar
Revising the reproductive story: psychosocial and reproductive impacts 12 months after reproductive genetic carrier screening
E. Tutty, B. McClaren, Sharon Lewis, K. Barlow-Stewart +8 more
2025European Journal of Human Genetics2 citations Open access
Semantic Scholar
1. HMG CoA SYNTHASE DEFICIENCY- HOW COMMON IS IT AND HOW GOOD ARE OUR MARKERS?
S. Brown, S. Thompson, J. Christodoulou, C. Ellaway +9 more
20121 citations
Semantic Scholar
Cystic fibrosis cascade carrier testing in Victoria, Australia
B. McClaren
20101 citations
Semantic Scholar
Cascade carrier testing for cystic fibrosis: an Australian experience
B. McClaren, Maryanne Aitken, R. Massie, S. Metcalfe +1 more
20081 citations Open access
Semantic Scholar
Clinical Genomics: Integrated teamworking across the sociotechnical divide
S. Best, Janet C. Long, J. Braithwaite, Zornitza Stark +8 more
2021International Journal of Integrated Care0 citations Open access
Semantic Scholar
Title, Table of Contents and Acknowledgment
Shirin Heidari, Claudia Garcia, Khuloud Alsaba, A. Kapilashrami +23 more
20160 citations Open access
Semantic Scholar
Women’s and men’s experiences of disclosure of a fetal abnormality
Penelope Pitt, S. Metcalfe, J. Halliday, J. Fisher +5 more
20150 citations
Semantic Scholar

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