The Role of Genomic Copy Number Variation in Regulation of Bone Disease Phenotypes

Wilson, Scott (Investigator 01)
Prince, Richard (Investigator 02)

Status	Finished
Effective start/end date	1/01/11 → 31/12/13

Funding

NHMRC National Health and Medical Research Council : A$424,615.00
NHMRC National Health and Medical Research Council : A$424,615.00

Access Project

http://purl.org/au-research/grants/nhmrc/1010494

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
Mullin, B., Tickner, J., Zhu, K., Kenny, J., Mullin, S., Brown, S. J., Dudbridge, F., Pavlos, N., Mocarski, E. S., Walsh, J. P., Xu, J. & Wilson, S., 26 Mar 2020, In: Genome Biology. 21, 1, 80.
Research output: Contribution to journal › Article › peer-review

Open Access
58 Link opens in a new tab Citations (Scopus)
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes
Ruth, K. S., Campbell, P. J., Chew, S., Lim, E. M., Hadlow, N., Stuckey, B., Brown, S. J., Feenstra, B., Joseph, J., Surdulescu, G. L., Zheng, H. F., Richards, J. B., Murray, A., Spector, T. D., Wilson, S. & Perry, J. R. B., 1 Feb 2016, In: European Journal of Human Genetics. 24, 2, p. 284-290 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
93 Link opens in a new tab Citations (Scopus)