Michel Michaelides

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the α subunit of cone transducin (GNAT2)

D. Hunt, T. Forshew, R. Trembath, 2002, Journal of medical genetics.

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2)

J. Mollon, D. Hunt, M. Michaelides, 2003, The British journal of ophthalmology.

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1.

F. Cremers, F. Raymond, K. Carss, 2016, Investigative ophthalmology & visual science.

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals

J. Mollon, D. Hunt, G. Holder, 2005, Eye.

Visual Psychophysics and Physiological Optics Vision in Observers With Enhanced SCone Syndrome : An Excess of SCones but Connected Mainly to Conventional SCone Pathways

A. Stockman, C. Ripamonti, P. Sergouniotis, 2014 .