Rod pathways: the importance of seeing nothing von Sharpe, Lindsay T., Stockman, Andrew

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Sex-related differences in chromatic sensitivity von RODRÍGUEZ-CARMONA, M., SHARPE, L.T., HARLOW, J.A., BARBUR, J.L.

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The spectral sensitivity of the human short-wavelength sensitive cones derived from thresholds and color matches von Stockman, Andrew, Sharpe, Lindsay T., Fach, Clemens

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Prevalence, demographic variation and psychological correlates of exposure to police victimisation in four US cities von DeVylder, J. E., Oh, H. Y., Nam, B., Sharpe, T. L., Lehmann, M., Link, B. G.

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Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21 von KOHL, S, BAUMANN, B, WISSINGER, B, BROGHAMMER, M, JÄGLE, H, SIEVING, P, KELLNER, U, SPEGAL, R, ANASTASI, M, ZRENNER, E, SHARPE, L. T

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Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel von Kohl, Susanne, Marx, Tim, Giddings, Ian, Jägle, Herbert, Jacobson, Samuel G., Apfelstedt-Sylla, Eckhart, Zrenner, Eberhart, Sharpe, Lindsay T., Wissinger, Bernd

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The spectral sensitivities of the middle- and long-wavelength-sensitive cones derived from measurements in observers of known genotype von Stockman, Andrew, Sharpe, Lindsay T.

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Asymmetries in the time-course of chromatic adaptation and the significance of contrast von Werner, Annette, Sharpe, Lindsay T., Zrenner, Eberhart

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Macular pigment densities derived from central and peripheral spectral sensitivity differences von Sharpe, Lindsay T, Stockman, Andrew, Knau, Holger, Jägle, Herbert

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia von Kohl, Susanne, Varsanyi, Balazs, Antunes, Gesine Abadin, Baumann, Britta, Hoyng, Carel B, Jägle, Herbert, Rosenberg, Thomas, Kellner, Ulrich, Lorenz, Birgit, Salati, Roberto, Jurklies, Bernhard, Farkas, Agnes, Andreasson, Sten, Weleber, Richard G, Jacobson, Samuel G, Rudolph, Günther, Castellan, Claudio, Dollfus, Helene, Legius, Eric, Anastasi, Mario, Bitoun, Pierre, Lev, Dorit, Sieving, Paul A, Munier, Francis L, Zrenner, Eberhart, Sharpe, Lindsay T, Cremers, Frans P M, Wissinger, Bernd

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M-cone opsin gene number does not correlate with variation in L/M-cone sensitivity von Knau, H, Kremers, J, Schmidt, H.-J, Wolf, S, Wissinger, B, Sharpe, L.T

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Flicker cone electroretinogram in dichromats and trichromats von Usui, Tomoaki, Kremers, Jan, Sharpe, Lindsay T, Zrenner, Eberhart

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CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders von Wissinger, Bernd, Gamer, Daphne, Jägle, Herbert, Giorda, Roberto, Marx, Tim, Mayer, Simone, Tippmann, Sabine, Broghammer, Martina, Jurklies, Bernhard, Rosenberg, Thomas, Jacobson, Samuel G., Sener, E. Cumhur, Tatlipinar, Sinan, Hoyng, Carel B., Castellan, Claudio, Bitoun, Pierre, Andreasson, Sten, Rudolph, Günter, Kellner, Ulrich, Lorenz, Birgit, Wolff, Gerhard, Verellen-Dumoulin, Christine, Schwartz, Marianne, Cremers, Frans P.M., Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Salati, Roberto, Sharpe, Lindsay T., Kohl, Susanne

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Human cone spectral sensitivities: a progress report von Stockman, Andrew, Sharpe, Lindsay T.

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Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11 von Wissinger, Bernd, Jägle, Herbert, Kohl, Susanne, Broghammer, Martina, Baumann, Britta, Hanna, David B, Hedels, Christian, Apfelstedt-Sylla, Eckhard, Randazzo, Giorgio, Jacobson, Samuel G, Zrenner, Eberhart, Sharpe, Lindsay T

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Reorganization of human cortical maps caused by inherited photoreceptor abnormalities von Baseler, Heidi A., Brewer, Alyssa A., Sharpe, Lindsay T., Morland, Antony B., Jägle, Herbert, Wandell, Brian A.

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New Aspects of an Old Theme: The Genetic Basis of Human Color Vision von Wissinger, Bernd, Sharpe, Lindsay T.

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Response phase of the flicker electroretinogram (ERG) is influenced by cone excitation strength von Usui, Tomoaki, Kremers, Jan, Sharpe, Lindsay T., Zrenner, Eberhart

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Hue memory and discrimination in young children von Petzold, Axel, Sharpe, Lindsay T.

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Is colour vision possible with only rods and blue-sensitive cones ? von REITNER, A, SHARPE, L. T, ZRENNER, E

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