Campbell, Purdey J.
Sir Charles Gairdner Hospital
6 papers on CoChatORCID 0000-0002-5727-4323
Most cited papers
- Verified
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer, A., Chaker, L., Groeneweg, S., Li, Y., Di Munno, C., Barbieri, C., Schultheiss, U. T., Traglia, M., Ahluwalia, T. S., Akiyama, M., et al. (2018) · Nature Communications
Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology
Cited by 280
- Verified
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. G., Brown, S. J., Feenstra, B., Joseph, J., Surdulescu, G. L., et al. (2016) · European Journal of Human Genetics
Genetic Associations and EpidemiologySexual Differentiation and Disorders
Cited by 121
- Verified
Whole-genome sequence-based analysis of thyroid function
Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., et al. (2015) · Nature Communications
Genetic Associations and EpidemiologyThyroid Disorders and Treatments
Cited by 104
- Verified
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications.
Sterenborg, R. B. T. M., Steinbrenner, I., Li, Y., Bujnis, M. N., Naito, T., Marouli, E., Galesloot, T. E., Babajide, O., Andreasen, L., Astrup, A., et al. (2024) · Nature Communications
Genetic Associations and EpidemiologyThyroid Disorders and Treatments
Cited by 79
- Verified
Changes in Thyroid Function Across Adolescence: A Longitudinal Study
Campbell, P. J., Brown, S. J., Kendrew, P., Lewer, M., Lim, E. M., Joseph, J., Cross, S. M., Wright, M. J., Martin, N. G., Wilson, S. G., et al. (2020) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGrowth Hormone and Insulin-like Growth Factors
Cited by 22
- Verified
Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With KLF9 and DOT1L
Lafontaine, N., Campbell, P. J., Castillo-Fernandez, J. E., Mullin, S., Lim, E. M., Kendrew, P., Lewer, M., Brown, S. J., Huang, R.-C., Melton, P. E., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism
Epigenetics and DNA MethylationThyroid Disorders and Treatments
Cited by 17
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