Lindsay T. Sharpe - Concepedia

Author

Lindsay T. Sharpe

Also Known As

L Sharpe, L T Sharpe, L. T. Sharpe, L.T Sharpe, L.T. SHARPE, L.T. Sharpe, LINDSAY T. SHARPE, Lindsay Sharpe, Lindsay T Sharpe, Lindsay T. Sharpe

125

Publications

7.2K

Citations

H-Index

Concepts

All Affiliations

University of Tübingen STZ eyetrial University of California San Diego University College London Universitäts-Augenklinik Bonn

About

Lindsay T. Sharpe is an author at University of Tübingen specializing in ophthalmology, neuroscience, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	1.6K
2	Engineering	8	8	1.4K
3	Health Sciences	4	4	263
4	Natural Sciences	3	3	367
5	Public Health	1	1	69

Lindsay T. Sharpe

Publications

5.8K

Citations

H-Index

Page 1

	Year	Citations
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 Spectral SensitivitiesEngineeringMeasurementOptical PropertiesSpectroscopy	2000	880
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, Nature Genetics BiologyPhotoreceptor CellRetinaOphthalmologyPhotosystems	1998	338
CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders Bernd Wissinger, Daphne Gamer, Herbert Jägle, The American Journal of Human Genetics Photoreceptor CellOphthalmologyGenetic DisorderGeneticsCnga3 Mutations	2001	321
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 Photoreceptor CellOphthalmologyPhysiological OpticOptical PropertiesSpectroscopy	1999	288
Opsin genes, cone photopigments, color vision, and color blindness Lindsay T. Sharpe Photoreceptor CellRetinaOphthalmologyOpsin GenesMedicine	1999	267
The contributions of color to recognition memory for natural scenes. Felix A. Wichmann, Lindsay T. Sharpe, Karl R. Gegenfurtner Journal of Experimental Psychology Learning Memory and Cognition EngineeringCognitionAttentionSocial SciencesPsychology	2002	259
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia Susanne Kohl, Balázs Varsányi, Gesine Abadin Antunes, European Journal of Human Genetics Autosomal Recessive AchromatopsiaMendelian DisorderGenetic DisorderGeneticsClinical Genetics	2004	244
A luminous efficiency function,<i>V</i>*(<i>λ</i>), for daylight adaptation Lindsay T. Sharpe, Andrew Stockman, Wolfgang Jagla, Journal of Vision	2005	221
Genetic heterogeneity among blue-cone monochromats. Jeremy Nathans, Irene H. Maumenee, Eberhart Zrenner, PubMed	1993	203
Reorganization of human cortical maps caused by inherited photoreceptor abnormalities Heidi A. Baseler, Alyssa A. Brewer, Lindsay T. Sharpe, Nature Neuroscience Photoreceptor CellRetinaOphthalmologyDevelopmental Cognitive NeuroscienceNeuroanatomy	2002	178

Page 1