Ms Bronwyn Terrill

Conjoint Lecturer

Master of Education (specialising in Educational Technologies), Monash University. Research: Exploring opportunities to develop students’ genomic literacy – as a subset of scientific literacy – in Australian secondary schools

Graduate Certificate of Applied Science (Scientific & Technical Writing), Deakin University

Graduate Diploma of Education (Secondary: Biology and Chemistry), Monash University

Graduate Diploma in Scientific Communication (Distinction), Australian National University

Bachelor of Science (Biochemistry, Organic Chemistry), University of Queensland, Brisbane

Medicine & Health
School of Clinical Medicine

Bronwyn is a science communicator, educator, researcher and writer working at the Garvan Institute of Medical Research in the Centre for Population Genomics. She focuses on developing strategic approaches to implementation of genomic medicine, often through engaging and educating public and professional audiences. She is an investigator on national projects focused on genomics workforce and education, genetic literacy, teaching with molecular animations, and community engagement with genomics. 

In past roles in Australia, the US and UK, Bronwyn has focused on engaging different audiences with genetics, genomics and molecular biology. She has coordinated a national network of genomics educators, curated museum exhibitions in Australia, the US and the UK, and developed education programs for school students, teachers, professionals and public audiences. Bronwyn produced award-winning online resources for Cold Spring Harbor Laboratory’s Dolan DNA Learning Center on molecular biology, genetics and cancer. She also established and managed the public engagement team for the largest genome centre in Europe, the Wellcome Trust Sanger Institute.

Throughout her career, Bronwyn’s focus has shifted between collaborations generating data and experience, directly producing resources, advising on large public projects and enabling researchers in their own public engagement efforts. She has advised on exhibitions for the Science Museum and Natural History Museum in London, and significantly contributed to innovative education and public engagement collaborations, including educational resources, travelling exhibitions and events, alternate reality games, and a range of broadcast media.

Phone
0458454546
  • Book Chapters | 2025
    Ailabouni NJ; Terrill B; Freeman CR, 2025, 'The Power of the Consumer Voice in Knowledge Translation of Deprescribing', in Advanced Clinical Pharmacy - Research, Development and Practical Applications, Springer Nature Switzerland, pp. 131 - 157, http://dx.doi.org/10.1007/978-3-031-77314-3_5
    Book Chapters | 2007
    Terrill B, 2007, 'Communication by scientists or stars?', in Journalism Science and Society Science Communication Between News and Public Relations, pp. 183 - 192, http://dx.doi.org/10.4324/9780203942314
  • Journal articles | 2025
    Dunlop KLA; Singh N; Smit AK; Morrow AL; Steinberg J; Cust AE; Makeham M; Bonner C; Terrill B; Monrouxe LV; Wilkinson D; Sawleshwarkar S; Ma AS, 2025, 'Building capacity for genomics in primary care: a scoping review of practitioner attitudes, education needs, and enablers', Frontiers in Medicine, 12, http://dx.doi.org/10.3389/fmed.2025.1577958
    Journal articles | 2025
    Dunn M; Strnadová I; Tso M; Mardones CP; Boyle J; Longhurst E; Refalo JL; Sarfaraz S; Terrill B; Palmer EE, 2025, 'Shared Decision-Making for Genetic Tests With Children and Young People With Intellectual Disability: Considerations for Inclusive, Person-Centred, and Respectful Approaches', Journal of Paediatrics and Child Health, http://dx.doi.org/10.1111/jpc.70202
    Journal articles | 2025
    Jackaman KM; Strnadová I; Willow SA; Loblinzk Refalo J; Scully JL; Palmer EE; Terrill B; Bromwich S, 2025, 'Developing genetic literacy in high school students with intellectual disability: Teachers’ experiences and perspectives', European Journal of Human Genetics, 33, pp. 1530 - 1538, http://dx.doi.org/10.1038/s41431-025-01865-2
    Journal articles | 2025
    Mackley MP; Agrawal PB; Ali SS; Archibald AD; Dawson-McClaren B; Ellard H; Freeman L; Gu Y; Jayasinghe K; Jiang S; Kirk EP; Lewis C; McEwen A; Nisselle A; Quinlan C; Terrill B; Tutty E; McNeill A, 2025, 'Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation', European Journal of Human Genetics, 33, pp. 1402 - 1413, http://dx.doi.org/10.1038/s41431-025-01925-7
    Journal articles | 2025
    McGahan E; Berkman J; Milne D; Terrill B; Gear R; Gardiner S; Eckstein L; Nicol D; Taylor N; Winship I; McWhirter R; Nisselle A; Lodge J; McInerney-Leo A, 2025, 'Empowering human research ethics committees to review genomics applications: evaluating the utility of a custom online education resource', European Journal of Human Genetics, 33, pp. 945 - 955, http://dx.doi.org/10.1038/s41431-025-01846-5
    Journal articles | 2025
    Strnadová I; Dunn M; Molnar C; Loblinzk Refalo J; Scully JL; Danker J; Tso M; Lim TQ; Cathcart-King Y; Jackaman KM; Hayes S; Willow SA; Boyle J; Hansen J; Sarfaraz S; Basckin C; Halliburton C; Ganeshan TS; Middleton EK; Terrill B; Palmer EE, 2025, 'Erratum: “All doctors should be trained in that”: The co-production and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disability (Genetics in Medicine (2025) 27(4), (S1098360025000188), (10.1016/j.gim.2025.101371))', Genetics in Medicine, 27, http://dx.doi.org/10.1016/j.gim.2025.101499
    Journal articles | 2025
    Strnadová I; Dunn M; Molnar C; Loblinzk Refalo J; Scully JL; Danker J; Tso M; Lim TQ; Cathcart-King Y; Jackaman KM; Hayes S; Willow SA; Boyle J; Hansen J; Sarfaraz S; Basckin C; Halliburton C; Sri Ganeshan T; Middleton EK; Terrill B; Palmer EE; Loblinzk J; Bromwich S, 2025, '“All doctors should be trained in that”: The coproduction and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disability', Genetics in Medicine, 27, pp. 101371, http://dx.doi.org/10.1016/j.gim.2025.101371
    Journal articles | 2025
    Villani RM; Terrill B; Tudini E; McKenzie ME; Cliffe CC; Hahn CN; Lundie B; Mattiske T; Matotek E; McEwen AE; Nickerson SL; Breen J; Fowler DM; Christodoulou J; Starita L; Rubin AF; Spurdle AB, 2025, 'Consultation informs strategies for improving the use of functional evidence in variant classification', American Journal of Human Genetics, 112, pp. 1489 - 1495, http://dx.doi.org/10.1016/j.ajhg.2025.05.003
    Journal articles | 2024
    Molnar C; Strnadová I; Dunn M; Loblinzk J; Sarfaraz S; Cathcart-King Y; Tso M; Danker J; Hayes S; Willow SA; Hansen J; Lim TQ; Boyle J; Terrill B; Scully JL; Palmer EE; Bromwich S, 2024, 'The need for co-educators to drive a new model of inclusive, person-centred and respectful co-healthcare with people with intellectual disability', Frontiers in Psychiatry, 15, pp. 1346423, http://dx.doi.org/10.3389/fpsyt.2024.1346423
    Journal articles | 2024
    Nisselle A; Terrill B; Janinski M; Martyn M; Jordan H; Kaunein N; Metcalfe S; Gaff C, 2024, 'Ensuring best practice in genomics education: A theory- and empirically informed evaluation framework', American Journal of Human Genetics, 111, pp. 1497 - 1507, http://dx.doi.org/10.1016/j.ajhg.2024.06.004
    Journal articles | 2024
    Nisselle A; Terrill B; Janinski M; Metcalfe S; Gaff C, 2024, 'Ensuring best practice in genomics education: A scoping review of genomics education needs assessments and evaluations', American Journal of Human Genetics, 111, pp. 1508 - 1523, http://dx.doi.org/10.1016/j.ajhg.2024.06.005
    Journal articles | 2024
    Pearce A; Mitchell LA; Best S; Young MA; Terrill B, 2024, 'Publics’ knowledge of, attitude to and motivation towards health-related genomics: a scoping review', European Journal of Human Genetics, 32, pp. 747 - 758, http://dx.doi.org/10.1038/s41431-024-01547-5
    Journal articles | 2024
    Terrill B; Pearce A; Chau A; Young M-A, 2024, 'Navigating genomic testing: Evaluation of an e-learning module with general practitioners', FOCUS ON HEALTH PROFESSIONAL EDUCATION-A MULTIDISCIPLINARY JOURNAL, 25, pp. 37 - 50
    Journal articles | 2023
    Nisselle A; King E; Terrill B; Davey B; McClaren B; Dunlop K; Graves D; Metcalfe S; Gaff C, 2023, 'Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation', Npj Genomic Medicine, 8, http://dx.doi.org/10.1038/s41525-023-00360-1
    Journal articles | 2023
    Terrill B; McKnight L; Pearce A; Gordon H; Lo W; Lee ICJ; Runiewicz M; Palmer A; Andrews L; Kirk E; Goldberg D; Tucker J; Murray D; Kaplan W; Kummerfeld S; Burnett L, 2023, 'Community Genetics screening in a pandemic: solutions for pre-test education, informed consent, and specimen collection', European Journal of Human Genetics, 31, pp. 257 - 261, http://dx.doi.org/10.1038/s41431-022-01251-2
    Journal articles | 2023
    Yanes T; Wallingford CK; Young MA; McInerney-Leo AM; Willis AM; McKnight L; Terrill B; McInerny S; Forrest LE; Cicciarelli L; Williams R; Keane H; James PA, 2023, 'Development and evaluation of a novel educational program for providers on the use of polygenic risk scores', Genetics in Medicine, 25, http://dx.doi.org/10.1016/j.gim.2023.100876
    Journal articles | 2022
    Lacaze PA; Tiller J; Winship I; Brotchie A; McNeil J; Zalcberg J; Thomas D; Milne R; James P; Delatycki M; Young MA; Nowak K; Nguyen-Dumont T; Southey M; Ademi Z; Bruinsma F; Riaz M; Terrill B; Kirk J; Tucker K; Andrews L; Pachter N; Susman R; Poplawski N; Wallis M; Watts G; Nicholls S; Macrae F; Sturm A; Green R; Ahern S; Revote J; Von Saldern S; Powell S; Rice T, 2022, 'Population DNA screening for medically actionable disease risk in adults', Medical Journal of Australia, 216, pp. 278 - 280, http://dx.doi.org/10.5694/mja2.51454
    Journal articles | 2022
    Patterson K; Terrill B; Dorfman BS; Blonder R; Yarden A, 2022, 'Molecular animations in genomics education: designing for whom?', Trends in Genetics, 38, pp. 517 - 520, http://dx.doi.org/10.1016/j.tig.2022.03.003
    Journal articles | 2022
    Pearce A; Terrill B; Alffenaar JW; Patanwala AE; Kummerfeld S; Day R; Young MA; Stocker SL, 2022, 'Pharmacogenomic testing: perception of clinical utility, enablers and barriers to adoption in Australian hospitals', Internal Medicine Journal, 52, pp. 1135 - 1143, http://dx.doi.org/10.1111/imj.15719
    Journal articles | 2022
    Primiero CA; Baker AM; Wallingford CK; Maas EJ; Yanes T; Fowles L; Janda M; Young MA; Nisselle A; Terrill B; Lodge JM; Tiller JM; Lacaze P; Andersen H; McErlean G; Turbitt E; Soyer HP; McInerney-Leo AM, 2022, 'Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma', Frontiers in Genetics, 13, http://dx.doi.org/10.3389/fgene.2022.919134
    Journal articles | 2022
    Willis AM; Terrill B; Pearce A; McEwen A; Ballinger ML; Young MA, 2022, 'My Research Results: a program to facilitate return of clinically actionable genomic research findings', European Journal of Human Genetics, 30, pp. 363 - 366, http://dx.doi.org/10.1038/s41431-021-00973-z
    Journal articles | 2021
    Cusack MB; Hickerton C; Nisselle A; McClaren B; Terrill B; Gaff C; Dunlop K; Metcalfe S, 2021, 'General practitioners' views on genomics, practice and education A qualitative interview study', Australian Journal of General Practice, 50, pp. 747 - 752, http://dx.doi.org/10.31128/AJGP-05-20-5448
    Journal articles | 2021
    McKnight L; Pearce A; Willis A; Young MA; Terrill B, 2021, 'Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology', Journal of Community Genetics, 12, pp. 653 - 662, http://dx.doi.org/10.1007/s12687-021-00550-3
    Journal articles | 2021
    Nisselle A; Janinski M; Martyn M; McClaren B; Kaunein N; Maguire J; Riggs ER; Barlow-Stewart K; Belcher A; Bernat JA; Best S; Bishop M; Carroll JC; Cornel M; Dissanayake VHW; Dodds A; Dunlop K; Garg G; Gear R; Graves D; Knight K; Korf B; Kumar D; Laurino M; Ma A; Mallett A; McCarthy M; McEwen A; Mulder N; Patel C; Quinlan C; Reed K; Sinnerbrink I; Slavotinek A; Suppiah V; Terrill B; Tobias ES; Tonkin E; Trumble S; Wessels TM; Metcalfe S; Jordan H; Gaff C, 2021, 'Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)', Genetics in Medicine, 23, pp. 1356 - 1365, http://dx.doi.org/10.1038/s41436-021-01140-x
    Journal articles | 2021
    Nisselle A; King EA; McClaren B; Janinski M; Metcalfe S; Gaff C; Dunlop K, 2021, 'Measuring physician practice, preparedness and preferences for genomic medicine: a national survey', BMJ OPEN, 11, http://dx.doi.org/10.1136/bmjopen-2020-044408
    Journal articles | 2021
    Pysar R; Wallingford CK; Boyle J; Campbell SB; Eckstein L; McWhirter R; Terrill B; Jacobs C; McInerney-Leo AM, 2021, 'Australian human research ethics committee members’ confidence in reviewing genomic research applications', European Journal of Human Genetics, 29, pp. 1811 - 1818, http://dx.doi.org/10.1038/s41431-021-00951-5
    Journal articles | 2021
    Tutty E; Hickerton C; Terrill B; McClaren B; Tytherleigh R; Stackpoole E; Savard J; Newson A; Middleton A; Nisselle A; Cusack M; Adamski M; Gaff C; Metcalfe S, 2021, 'The expectations and realities of nutrigenomic testing in australia: A qualitative study', Health Expectations, 24, pp. 670 - 686, http://dx.doi.org/10.1111/hex.13216
    Journal articles | 2020
    Savard J; Terrill B; Dunlop K; Samanek A; Metcalfe SA, 2020, 'Human Genetics Society of Australasia Position Statement: Online DNA Testing', Twin Research and Human Genetics, 23, pp. 256 - 258, http://dx.doi.org/10.1017/thg.2020.67
    Journal articles | 2019
    Dorfman BS; Terrill B; Patterson K; Yarden A; Blonder R, 2019, 'Teachers personalize videos and animations of biochemical processes: results from a professional development workshop', Chemistry Education Research and Practice, 20, pp. 772 - 786, http://dx.doi.org/10.1039/c9rp00057g
    Journal articles | 2019
    Dwarte T; Barlow-Stewart K; O’Shea R; Dinger ME; Terrill B, 2019, 'Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners', Journal of Genetic Counseling, 28, pp. 378 - 387, http://dx.doi.org/10.1002/jgc4.1053
    Journal articles | 2019
    Fleming J; Terrill B; Dziadek M; Kirk EP; Roscioli T; Barlow-Stewart K, 2019, 'Personal genomic screening: How best to facilitate preparedness of future clients', European Journal of Medical Genetics, 62, pp. 397 - 404, http://dx.doi.org/10.1016/j.ejmg.2019.05.006
    Journal articles | 2019
    Metcalfe SA; Hickerton C; Savard J; Stackpoole E; Tytherleigh R; Tutty E; Terrill B; Turbitt E; Gray K; Middleton A; Wilson B; Newson AJ; Gaff C, 2019, 'Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study', European Journal of Medical Genetics, 62, pp. 290 - 299, http://dx.doi.org/10.1016/j.ejmg.2018.11.002
    Journal articles | 2019
    Nisselle A; Martyn M; Jordan H; Kaunein N; McEwen A; Patel C; Terrill B; Bishop M; Metcalfe S; Gaff C, 2019, 'Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic Approach', Frontiers in Genetics, 10, pp. 1057, http://dx.doi.org/10.3389/fgene.2019.01057
    Journal articles | 2019
    Savard J; Hickerton C; Tytherleigh R; Terrill B; Turbitt E; Newson AJ; Wilson B; Gray K; Gaff C; Middleton A; Stackpoole E; Metcalfe SA, 2019, 'Australians’ views and experience of personal genomic testing: survey findings from the Genioz study', European Journal of Human Genetics, 27, pp. 711 - 720, http://dx.doi.org/10.1038/s41431-018-0325-x
    Journal articles | 2018
    Metcalfe SA; Hickerton C; Savard J; Terrill B; Turbitt E; Gaff C; Gray K; Middleton A; Wilson B; Newson AJ, 2018, 'Australians’ views on personal genomic testing: focus group findings from the Genioz study', European Journal of Human Genetics, 26, pp. 1101 - 1112, http://dx.doi.org/10.1038/s41431-018-0151-1
    Journal articles | 2017
    Gray K; Stephen R; Terrill B; Wilson B; Middleton A; Tytherleigh R; Turbitt E; Gaff C; Savard J; HIckerton C; Newson A; Metcalfe S, 2017, 'Consumer health informatics aspects of direct-to-consumer personal genomic testing', Studies in Health Technology and Informatics, 245, http://dx.doi.org/10.3233/978-1-61499-830-3-89
    Journal articles | 2017
    Gray K; Stephen R; Terrill B; Wilson B; Middleton A; Tytherleigh R; Turbitt E; Gaff C; Savard J; Hickerton C; Newson A; Metcalfe S, 2017, 'Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing', Europe PMC, 245, pp. 89 - 93, http://europepmc.org/abstract/med/29295058
    Journal articles | 2014
    Mattick JS; Dziadek MA; Terrill BN; Kaplan W; Spigelman AD; Bowling FG; Dinger ME, 2014, 'The impact of genomics on the future of medicine and health', Medical Journal of Australia, 201, pp. 17 - 20, http://dx.doi.org/10.5694/mja13.10920
  • Preprints | 2025
    Clark A; Wallingford CK; Berkman J; McInerney-Leo A; Nisselle A; Terrill B; Palpant N; Young M-A; James P; Yanes T, 2025, An exploration of healthcare providers’ learning needs and strategies for engagement in Polygenic Risk education, http://dx.doi.org/10.1101/2025.07.17.25331741
    Preprints | 2025
    Strnadová I; Hansen J; Danker J; Jackaman K-M; Loblinzk J; Sarfaraz S; Scully JL; Boyle J; Terrill B; Palmer E, 2025, “It was up to me to be curious”: Perceptions and Experiences of Students with Intellectual Disability on Genetics and Health Education, http://dx.doi.org/10.21203/rs.3.rs-5635751/v1
    Preprints | 2025
    Villani RM; Terrill B; Tudini E; Matotek E; Mattiske T; Cliffe C; Thompson B; Satgunaseelan L; Hahn C; Lundie B; Christodoulou J; Rubin A; Spurdle A, 2025, Community co-designed workshops build confidence in use of functional evidence for variant classification, http://dx.doi.org/10.1101/2025.11.10.25339935
    Conference Papers | 2024
    Strnadova I; Jackaman K-M; Hansen J; Loblinzk J; Dunn M; Sarfaraz S; Hurd S; Danker J; Tso M; Willow SA; Molnar C; Boyle J; Scully JL; Palmer E; Terrill B, 2024, 'GeneEQUAL Schools: Health and genetic health literacy education for students with intellectual disabilities: Teachers' and students' experiences and perspectives', in EUROPEAN JOURNAL OF HUMAN GENETICS, SPRINGERNATURE, GERMANY, Berlin, pp. 1225 - 1225, presented at 57th Conference of the European-Society-of-Human-Genetics (ESHG), GERMANY, Berlin, 01 June 2024 - 04 June 2024
    Preprints | 2024
    Villani RM; Terrill B; Tudini E; McKenzie ME; Cliffe CC; Hahn CN; Lundie B; Mattiske T; Matotek E; McEwen AE; Nickerson SL; Breen J; Fowler DM; Christodoulou J; Starita L; Rubin AF; Spurdle AB, 2024, Consultation informs strategies to improve functional evidence use in variant classification., http://dx.doi.org/10.1101/2024.12.04.24318523
    Conference Papers | 2023
    Abeygunawardena D; Oates E; Palmer E; Terrill B, 2023, '“I FEEL MUCH MORE CONFIDENT IN APPROACHING GENETICS IN MY WORKPLACE...”: A SHORT COURSE IN PRACTICAL MEDICAL GENOMICS', in INTED Proceedings, IATED, pp. 8406 - 8406, presented at 17th International Technology, Education and Development Conference, 06 March 2023 - 07 March 2023, http://dx.doi.org/10.21125/inted.2023.2311
    Preprints | 2023
    Yanes T; Wallingford C; Young MA; McInerney-Leo AM; Willis A; McKnight L; Terrill B; McInerny S; Forrest L; Cicciarelli L; Williams R; Keane H; James PA, 2023, Development and evaluation of a novel educational program for providers on the use of polygenic risk scores, http://dx.doi.org/10.1101/2023.02.16.23286057
    Conference Abstracts | 2022
    Hesson L; Hobbs M; Low C; Copty J; Murray D; Stocker S; Terrill B; Kaplan W; Galea M; Suthers G, 2022, 'IS PHARMACOGENETIC TESTING RELEVANT TO PSYCHIATRIC MEDICATIONS IN AN AUSTRALIAN POPULATION?', in AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, SAGE PUBLICATIONS LTD, Vol. 56, pp. 212 - 213, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000792769900498&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Abstracts | 2021
    Willis A; Terrill B; Pearce A; McEwen A; Ballinger M; Milne R; Bruinsma F; Tiller J; Lacaze P; Young M-A, 2021, 'My Research Results supporting researchers to return clinically actionable genetic research findings', in ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, WILEY, Vol. 17, pp. 36 - 37, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000693805000064&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Papers | 2019
    Wilson B; Savard J; Hickerton C; Terrill B; Newson A; Gaff C; Gray K; Middleton A; Metcalfe S, 2019, '12 ‘Recreational’ consumer genomics: no such thing as a non-medical test', in Poster Presentations, BMJ Publishing Group Ltd, pp. A58.1 - A58, presented at Preventing Overdiagnosis Abstracts, December 2019, Sydney, Australia, http://dx.doi.org/10.1136/bmjebm-2019-pod.118
    Conference Abstracts | 2018
    McClaren B; Prichard Z; Nisselle AE; Crellin E; Janinski M; Ng L; Zilliacus E; Dunlop K; Graves D; Terrill B; Newson A; Gaff C; Metcalfe SA, 2018, 'The changing clinical practice of genomic medicine: what are the preferences of and education/training needs of health professionals?', in EUROPEAN JOURNAL OF HUMAN GENETICS, NATURE PUBLISHING GROUP, ITALY, Milan, Vol. 27, pp. 700 - 700, presented at 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), ITALY, Milan, 16 June 2018 - 19 June 2018, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000489313105160&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Abstracts | 2018
    Savard J; Hickerton C; Metcalfe S; Terrill B; Newson A; Gaff C; Gray K; Middleton A; Wilson B, 2018, 'Working with the public: engaging with consumers about the ethics of and decision to pursue personal genomic testing', in EUROPEAN JOURNAL OF HUMAN GENETICS, NATURE PUBLISHING GROUP, ITALY, Milan, Vol. 27, pp. 692 - 692, presented at 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), ITALY, Milan, 16 June 2018 - 19 June 2018, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000489313105144&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Abstracts | 2018
    Tutty E; Hickerton C; Adamski M; Savard J; Terrill B; Newson A; Gaff C; Gray K; Middleton A; Wilson B; Metcalfe S, 2018, '"I just wanted answers": Exploring personal genomic testing for nutrition and wellness', in EUROPEAN JOURNAL OF HUMAN GENETICS, NATURE PUBLISHING GROUP, ITALY, Milan, Vol. 27, pp. 742 - 743, presented at 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), ITALY, Milan, 16 June 2018 - 19 June 2018, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000489313105252&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Papers | 2017
    Metcalfe SA; Tytherleigh R; Hickerton C; Savard J; Terrill B; Turbitt E; Stackpoole E; Gaff C; Gray K; Middleton A; Wilson B; Newson A, 2017, 'Australian public's awareness, use and interest in health-related and recreational personal genomic testing', in EUROPEAN JOURNAL OF HUMAN GENETICS, NATURE PUBLISHING GROUP, DENMARK, Copenhagen, pp. 802 - 803, presented at 50th European-Society-of-Human-Genetics (ESHG) Conference, DENMARK, Copenhagen, 27 May 2017 - 30 May 2017, http://dx.doi.org/10.26190/unsworks/27629

My Health Care Choices My Way 2025/MRF2044902 2025-2030 (CI) Developing practical resources to help young people with intellectual disability navigate the shift from paediatric to adult health care.

Enabling inclusive population-scale genomics through culturally appropriate participant information, innovation in language translation, and workforce development 2025/MRF2045161 2025-2027 (CI) Developing co-designed translated materials, approaches to translation and education for researchers and bicultural workers.

CYP2C19 genetic testing to enhance antiplatelet drug safety and efficacy 2025/MRF2045096 2025-2031 (AI) Implementing of a pharmacogenomics testing service to prevent blood clots after heart procedures.

Diagnosis4All: Co-designing Equitable and Sustainable Solutions to Reduce the Diagnostic Odyssey 2025/MRF2045062 2025-2027 (AI) Co-designing solutions to improve rare care in multicultural communities.

Barriers and Enablers to Education on Genomic Health for Primary and High School Students with Intellectual Disability PS68387 2022-2025 (CI) DEI ADA Faculty Research Grants, UNSW Sydney. Improving the education students with intellectual disability learn about genetic health care in schools.

A national platform for evaluation and integration of advanced analytics in the diagnosis of genetic disease 
2024/MRF2032931 2024-2028 (CI) Capacity building for diagnostic health professionals in use of AI.

PRECISE (Practitioner Readiness, Education and Capabilities, with Implementation Science Evaluation) Genomics Research Project MRFF 2023/MRF2024995 2023-2026 (AI) Genomics education for primary practitioners.

Trial Integration of Polygenic Scores for Common Cancers into Standard Clinical Care 2023/MRF2024994
2023-2027 (CI) Collaborating on educational supports for genetic health professionals using polygenic scores.

Preparing Australia for Genomic Medicine and Australian Genomics NHMRC 113531 2015-2020 (one of 83 CIs); Member of the Working Group for Genomic Workforce and Education. 2024/GNT2035846 2024-2025 (AI).

Understanding the Australian public's expectations of personalised genomics ARC DP 150100597 2015-2018 (PI) Public attitudes, knowledge and trust of online DNA testing informing position statements and education.

Bronwyn became directly involved in research in 2015 in areas that span genetic literacy, genomics education in health, and public expectations of personal genomic tests.

Bronwyn is an investigator on the MRFF-funded DNAScreen genomic screening study (2021-2025). She is also an investigator on a subsection of the geneEQUAL study, researching genomics education in schools for people with intellectual disability. She was an investigator with the  Australian Genomics Health Alliance and a member of the Program 4 Working Group for Genomic Workforce, Education and Ethics, funded by the NHMRC for Preparing Australia for Genomic Medicine (113531; 2015-2020) and a partner investigator on the ARC-funded Genioz mixed-methods study (2015-2018 DP 150100597) Understanding the Australian public's expectations of personalised genomics and led the development of evidence-based resources on personal genomic tests. 

She is also working on international, national and local collaborations focused on

  • community awareness and genetic literacy regarding genomic technologies in genetic screening;
  • health professionals' attitudes to and knowledge of pharmacogenomic testing;
  • mainstreaming genomic testing;
  • teaching with molecular animations; and
  • community engagement with genomics and gene editing.