Bronwyn Terrill

ORCID: 0000-0003-0263-363X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • BRCA gene mutations in cancer
  • Ethics in Clinical Research
  • Genomics and Rare Diseases
  • Prenatal Screening and Diagnostics
  • Genetics, Bioinformatics, and Biomedical Research
  • Nutrition, Genetics, and Disease
  • Health Systems, Economic Evaluations, Quality of Life
  • Biomedical and Engineering Education
  • Cancer Genomics and Diagnostics
  • Child and Adolescent Health
  • Family and Disability Support Research
  • Disability Rights and Representation
  • Ethics and Legal Issues in Pediatric Healthcare
  • CRISPR and Genetic Engineering
  • Consumer Attitudes and Food Labeling
  • Genetically Modified Organisms Research
  • Primary Care and Health Outcomes
  • Genetic Associations and Epidemiology
  • Science Education and Pedagogy
  • Health and Medical Research Impacts
  • Cutaneous Melanoma Detection and Management
  • Colorectal Cancer Screening and Detection
  • Experimental Learning in Engineering
  • Bacillus and Francisella bacterial research
  • Biotechnology and Related Fields

UNSW Sydney
2018-2025

Garvan Institute of Medical Research
2014-2025

Melbourne Genomics Health Alliance
2019-2025

St Vincent's Health
2023-2025

Murdoch Children's Research Institute
2024

St Vincent's Clinic
2018-2022

Health First
2022

Despite healthcare professionals (HCP) endorsing the clinical utility of pharmacogenomics testing, use in practice is limited.To assess HCP' perceptions pharmacogenomic testing and identify barriers to implementation.HCP involved prescribing decisions at three hospitals Sydney, Australia, were invited participate. The online survey assessed including: (i) demographic variables; (ii) use, knowledge confidence; (iii) perceived benefits; (iv) implementation; (v) operational and/or system...

10.1111/imj.15719 article EN Internal Medicine Journal 2022-02-22

Australia will take a world-first step towards offering preventive DNA screening through the public health care system In adult-onset genomic conditions, such as hereditary breast and ovarian cancer (HBOC), Lynch syndrome familial hypercholesterolaemia, certain variants confer high risk of developing future disease.1 for these conditions could thereby identify medically actionable genetic factors, prompting timely management informed decision making from early adulthood to facilitate...

10.5694/mja2.51454 article EN cc-by-nc-nd The Medical Journal of Australia 2022-03-10

Abstract Genomic medicine is being implemented on a global scale, requiring genomic-competent health workforce. To inform education as part of implementation strategies to optimize adoption genomics by non-genetics physicians, we investigated current practices, perceptions and preferences relating genomic testing education. Australian physicians completed an online survey; conducted univariate multivariate analyses determinants confidence engagement with medicine. Confident or engaged...

10.1038/s41525-023-00360-1 article EN cc-by npj Genomic Medicine 2023-06-24

Targeted genomic education and training of professionals have been identified as core components strategies implementation plans for the use genomics in health care systems. Education needs to be effective support sustained appropriate care. Evaluation programs identify effectiveness is challenging. Furthermore, those responsible development delivery are not necessarily trained and/or evaluation. Program logic models used evaluation by articulating a logical explanation how program intends...

10.3389/fgene.2019.01057 article EN cc-by Frontiers in Genetics 2019-11-08

<title>Abstract</title> People with intellectual disability want to learn more about their health and genetics. They be empowered the knowledge skills make informed genetic healthcare choices. Little is known what high school students health, genetics or healthcare. To address this gap, we conducted an inclusive qualitative research study in Australia.<bold> </bold>Fourteen Australian current recently graduated participated semi-structured interviews. Inductive content analysis revealed four...

10.21203/rs.3.rs-5635751/v1 preprint EN cc-by Research Square (Research Square) 2025-01-09

Abstract Complex genomic technologies are increasingly utilised in research. However, human research ethics committee (HREC) members lack confidence reviewing genomics applications. This study developed and evaluated the acceptability utility of an online educational resource on ethical considerations for HREC members. Resource development evaluation was theoretically informed. Qualitative semi-structured interviews with subject experts were transcribed deductively analysed. Participants ( n...

10.1038/s41431-025-01846-5 article EN cc-by European Journal of Human Genetics 2025-04-17

Despite the advancements in production and accessibility of videos animations, a gap exists between their potential for science teaching actual use classroom. The aim this study was to develop evaluate an approach boost chemistry biology teachers’ Technological Pedagogical Content Knowledge (TPACK) confidence regarding animations class, which are required effective implementation. Twelve experienced high-school teachers participated professional development workshop including biochemistry...

10.1039/c9rp00057g article EN Chemistry Education Research and Practice 2019-01-01

Personal genomic testing using direct-to-consumer and consumer-directed models, with or without involvement of healthcare providers, is increasing internationally, including in Australia. This study forms a sub-set the Genioz - Genomics: National Insights Australians. We aimed to explore Australians' experiences these types tests, especially online DNA their views regarding whom they would seek support from around understanding test results. The used mixed methods approach, employing an...

10.1016/j.ejmg.2018.11.002 article EN cc-by-nc-nd European Journal of Medical Genetics 2018-11-12

Background and objectiveGenomics is moving rapidly into mainstream medicine through clinical genomic testing consumer-initiated online DNA testing.The aim of this study was to identify Australian general practitioners' (GPs') views on genomics, impact practice educational needs inform continuing education. MethodsSemi-structured interviews were conducted, with constant comparative inductive analysis governance from a national taskforce. ResultsTwenty-eight GPs (43% female) interviewed; 71%...

10.31128/ajgp-05-20-5448 article EN cc-by Australian Journal of General Practice 2021-09-30

Personal genomic tests (PGTs) for multiple purposes are marketed to ostensibly healthy people in Australia. These generally and purchased online commercially or can be ordered through a health professional. There has been minimal engagement with Australians about their interest experience ordering PGT. As part of multistage, interdisciplinary project, an survey (Stage 2 the Genioz study) was available from May 2016 2017. In total, 3253 respondents attempted survey, 2395 completed Australian...

10.1038/s41431-018-0325-x article EN cc-by European Journal of Human Genetics 2019-01-21

Personal genomic testing provides healthy individuals with access to information about their genetic makeup for purposes including ancestry, paternity, sporting ability and health. Such tests are available commercially globally, accessibility expected continue grow, in Australia; yet little is known of the views/expectations Australians. Focus groups were conducted within a multi-stage, cross-disciplinary project (Genioz) explore this. In mid-2015, 56 members public participated seven focus...

10.1038/s41431-018-0151-1 article EN cc-by European Journal of Human Genetics 2018-04-24

Abstract Facilitating informed decision‐making regarding genetic testing is a core component of counseling practice. Internationally, shifting toward gene panels and genomic testing, including whole exome genome sequencing to improve diagnostic yield cost‐effectiveness. This study explored genetics practitioners’ current experience with tests the associated evolution Genetics practitioners experience, were purposively invited participate in semi‐structured telephone interview snowball...

10.1002/jgc4.1053 article EN Journal of Genetic Counseling 2018-12-15

Background: Primary care, or general, practitioners (GPs) are increasingly expected to communicate with and support their patients through genetic genomic testing. However, GPs worldwide report a lack of knowledge about genetics what constitutes test. Few Australian educational resources for medical address core capabilities in genomics. Methods: We developed evaluated 90-minute online education module, Navigating Genomic Testing General Practice, hosted 12 months. The module aimed increase...

10.11157/fohpe.v25i1.630 article EN cc-by-nc-nd Focus on Health Professional Education A Multi-Professional Journal 2024-03-28
Coming Soon ...