Willoughby, Colin E.

Mutation Altering the miR-184 Seed Region Causes Familial Keratoconus with Cataract

Hughes, A. E., Bradley, D. T., Campbell, M., Lechner, J., Dash, D. P., Simpson, D. A., & Willoughby, C. E. (2011) · The American Journal of Human Genetics

Corneal surgery and disordersMicroRNA in disease regulation

Cited by 276

Mutational Analysis of MIR184 in Sporadic Keratoconus and Myopia

Lechner, J., Bae, H. A., Guduric-Fuchs, J., Rice, A., Govindarajan, G., Siddiqui, S., Abi Farraj, L., Yip, S. P., Yap, M., Das, M., et al. (2013) · Investigative Opthalmology & Visual Science

Corneal surgery and disordersMicroRNA in disease regulation

Cited by 78

Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus

Lechner, J., Porter, L. F., Rice, A., Vitart, V., Armstrong, D. J., Schorderet, D. F., Munier, F. L., Wright, A. F., Inglehearn, C. F., Black, G. C., et al. (2014) · Human Molecular Genetics

Corneal surgery and disordersConnective tissue disorders research

Cited by 72

Genome-wide transcriptome profiling of human trabecular meshwork cells treated with TGF-β2

Callaghan, B., Lester, K., Lane, B., Fan, X., Goljanek-Whysall, K., Simpson, D. A., Sheridan, C., & Willoughby, C. E. (2022) · Scientific Reports

Glaucoma and retinal disordersTGF-β signaling in diseases

Cited by 27

A Comparative Genome-Wide Transcriptome Analysis of Glucocorticoid Responder and Non-Responder Primary Human Trabecular Meshwork Cells

Kathirvel, K., Haribalaganesh, R., Krishnadas, R., Muthukkaruppan, V., Willoughby, C. E., Bharanidharan, D., & Senthilkumari, S. (2022) · Genes

Glaucoma and retinal disordersDrug-Induced Ocular Toxicity

Cited by 9

Main genetic entities associated with tooth agenesis

Cammarata-Scalisi, F., Willoughby, C. E., El-Feghaly, J. R., Tadich, A. C., Castillo, M. A., Alkhatib, S., Elsherif, M. A. E., El-Ghandour, R. K., Coletta, R., Morabito, A., et al. (2024) · Clinical Oral Investigations

dental development and anomaliesCleft Lip and Palate Research

Cited by 6