Cone Monochromacy
Cone Monochromacy is a rare form of inherited color vision deficiency characterized by the absence or non-functionality of two of the three cone photoreceptor types in the retina, resulting in severely reduced or absent color discrimination and reliance on a single cone type for photopic vision.
44
Publications
2.5K
Citations
240
Authors
133
Institutions
Publications per year
2017–2026
11
Parents
44
Molecular Genetics of Human Blue Cone Monochromacy
Jeremy Nathans, Carol Davenport, Irene H. Maumenee et al. · Science · 1989 · 326 citations
Genetic heterogeneity among blue-cone monochromats.
Jeremy Nathans, Irene H. Maumenee, Eberhart Zrenner et al. · PubMed · 1993 · 205 citations
Colour vision in aquatic mammals—facts and open questions
Ulrike Griebel, Leo Peichl · Aquatic Mammals · 2003 · 85 citations
Medicine, Vision Science, Zoology +17
1–5 of 44
240
8
h-index
8
h-index
5
h-index
5
h-index
4
h-index
1–5 of 240
133
STZ eyetrial
Tübingen, Germany
7 h-index
18 publications
570 citations
University College London
London, United Kingdom
6 h-index
23 publications
816 citations
University of Pennsylvania
Philadelphia, United States
5 h-index
26 publications
794 citations
University of Michigan
Ann Arbor, United States
4 h-index
17 publications
748 citations
Moorfields Eye Hospital
London, United Kingdom
4 h-index
14 publications
294 citations

Medical College of Wisconsin
Milwaukee, United States
4 h-index
7 publications
343 citations
Penn Presbyterian Medical Center
Philadelphia, United States
4 h-index
24 publications
656 citations

The University of Western Australia
Perth, Australia
4 h-index
13 publications
415 citations
1–8 of 133
Repository · 5 publications · 385 citations
5
h-index
3 publications · 92 citations
3
h-index
2 publications · 93 citations
2
h-index
2 publications · 119 citations
2
h-index
2 publications · 110 citations
2
h-index
1–5