|Novel genetic loci underlying human intracranial volume identified through genome-wide association|
HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Renterķa, ...
Nature neuroscience 19 (12), 1569-1582, 2016
|Cerebral small vessel disease genomics and its implications across the lifespan|
M Sargurupremraj, H Suzuki, X Jian, C Sarnowski, TE Evans, JC Bis, ...
Nature communications 11 (1), 6285, 2020
|Understanding public reactions to commercialization of biobanks and use of biobank resources|
D Nicol, C Critchley, R McWhirter, T Whitton
Social science & medicine 162, 79-87, 2016
|Community engagement for big epidemiology: deliberative democracy as a tool|
RE McWhirter, CR Critchley, D Nicol, D Chalmers, T Whitton, M Otlowski, ...
Journal of personalized medicine 4 (4), 459-474, 2014
|Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting|
G Chauhan, HHH Adams, CL Satizabal, JC Bis, A Teumer, ...
Neurology 92 (5), e486-e503, 2019
|Precision medicine: drowning in a regulatory soup?|
D Nicol, T Bubela, D Chalmers, J Charbonneau, C Critchley, J Dickinson, ...
Journal of Law and the Biosciences 3 (2), 281-303, 2016
|All in the blood: A review of Aboriginal Australians’ cultural beliefs about blood and implications for biospecimen research|
E Kowal, A Greenwood, RE McWhirter
Journal of Empirical Research on Human Research Ethics 10 (4), 347-359, 2015
|Identifying public expectations of genetic biobanks|
C Critchley, D Nicol, R McWhirter
Public understanding of science 26 (6), 671-687, 2017
|The complex genetics of gait speed: genome-wide meta-analysis approach|
D Ben-Avraham, D Karasik, J Verghese, KL Lunetta, JA Smith, JD Eicher, ...
Aging (Albany NY) 9 (1), 209, 2017
|Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic|
D Nicol, L Eckstein, M Morrison, JS Sherkow, M Otlowski, T Whitton, ...
Genome medicine 9, 1-4, 2017
|Equitable expanded carrier screening needs indigenous clinical and population genomic data|
S Easteal, RM Arkell, RF Balboa, SA Bellingham, AD Brown, T Calma, ...
The American Journal of Human Genetics 107 (2), 175-182, 2020
|Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders|
RE McWhirter, R McQuillan, E Visser, C Counsell, JF Wilson
European Journal of Human Genetics 20 (2), 198-202, 2012
|Runs of homozygosity and a cluster of vulvar cancer in young Australian Aboriginal women|
RE McWhirter, RJ Thomson, JR Marthick, AR Rumbold, MA Brown, ...
Gynecologic oncology 133 (3), 421-426, 2014
|Ethical genetic research in Indigenous communities: challenges and successful approaches☆|
RE McWhirter, D Mununggirritj, D Marika, JL Dickinson, JR Condon
Trends in Molecular Medicine 18 (12), 702-708, 2012
|Australia: regulating genomic data sharing to promote public trust|
L Eckstein, D Chalmers, C Critchley, R Jeanneret, R McWhirter, J Nielsen, ...
Human Genetics 137, 583-591, 2018
|The history of bioethics: implications for current debates in health research|
Perspectives in Biology and Medicine 55 (3), 329-338, 2012
|Moving forward on consent practices in Australia|
RE McWhirter, L Eckstein
Journal of Bioethical Inquiry 15, 243-257, 2018
|Genomics in research and health care with Aboriginal and Torres Strait Islander peoples|
R McWhirter, D Nicol, J Savulescu
Monash Bioethics Review 33, 203-209, 2015
|New avenues within community engagement: addressing the ingenuity gap in our approach to health research and future provision of health care|
D Chalmers, RE McWhirter, D Nicol, T Whitton, M Otlowski, MM Burgess, ...
Journal of Responsible Innovation 1 (3), 321-328, 2014
|Evidence for a common genetic aetiology in high‐risk families with multiple haematological malignancy subtypes|
EM Tegg, RJ Thomson, J Stankovich, A Banks, C Flowers, R McWhirter, ...
British journal of haematology 150 (4), 456-462, 2010