Lindsay T. Sharpe

The spectral sensitivities of the middle- and long-wavelength-sensitive cones derived from measurements in observers of known genotype

Andrew Stockman, Lindsay T. Sharpe · Vision Research · 2000 · 900 citations

Medicine, Biophysics, Vision Science +10

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Susanne Kohl, Tim Marx, Ian Giddings et al. · Nature Genetics · 1998 · 339 citations

Medicine, Genetics, Molecular Genetics +13

CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

Bernd Wissinger, Daphne Gamer, Herbert Jägle et al. · The American Journal of Human Genetics · 2001 · 326 citations · Full text

Medicine, Genetics, Molecular Genetics +14

The spectral sensitivity of the human short-wavelength sensitive cones derived from thresholds and color matches

Andrew Stockman, Lindsay T. Sharpe, Clemens Fach · Vision Research · 1999 · 292 citations

Medicine, Neuroscience, Vision Science +14

Opsin genes, cone photopigments, color vision, and color blindness

Lindsay T. Sharpe · 1999 · 267 citations

Medicine, Genetics, Molecular Genetics +17