Catherine J. Owen
Institute of Human Genetics
University of Newcastle
International Centre for Life
Central Parkway
UK
Name/email consistency: high
- Diagnosis and management of polyendocrinopathy syndromes. Owen, C.J., Cheetham, T.D. Endocrinol. Metab. Clin. North Am. (2009)
- Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association. Owen, C.J., Kelly, H., Eden, J.A., Merriman, M.E., Pearce, S.H., Merriman, T.R. J. Clin. Endocrinol. Metab. (2007)
- Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population. Owen, C.J., Eden, J.A., Jennings, C.E., Wilson, V., Cheetham, T.D., Pearce, S.H. J. Mol. Endocrinol. (2006)
- Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome. Owen, C.J., Jennings, C.E., Imrie, H., Lachaux, A., Bridges, N.A., Cheetham, T.D., Pearce, S.H. J. Clin. Endocrinol. Metab. (2003)