Inglehearn, Chris F.

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease

Woods, C. G., Cox, J., Springell, K., Hampshire, D. J., Mohamed, M. D., McKibbin, M., Stern, R., Raymond, F. L., Sandford, R., Malik Sharif, S., et al. (2006) · The American Journal of Human Genetics

Genetic Associations and EpidemiologyGenomics and Rare Diseases

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CFH,VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration

McKibbin, M., Ali, M., Bansal, S., Baxter, P. D., West, K., Williams, G., Cassidy, F., & Inglehearn, C. F. (2012) · British Journal of Ophthalmology

Retinal Diseases and TreatmentsOcular Diseases and Behçet’s Syndrome

Cited by 100

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

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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

Ultrastructural changes in the retinopathy, globe enlarged (rge) chick cornea

Boote, C., Hayes, S., Young, R. D., Kamma-Lorger, C. S., Hocking, P. M., Elsheikh, A., Inglehearn, C. F., Ali, M., & Meek, K. M. (2009) · Journal of Structural Biology

Corneal surgery and disordersOcular Disorders and Treatments

Cited by 37