Rod Monochromacy

Rod Monochromacy is a rare inherited form of complete color blindness characterized by the absence or non-functionality of all three types of cone photoreceptors in the retina, resulting in severely reduced visual acuity, photophobia, and a reliance on rod cells for all visual perception.

26

Publications

1.7K

Citations

112

Authors

74

Institutions

Publications per year

2017–2026

6

Variants

AchromatopsiaTotal Color Blindness

Authors

112

  1. SK
    Susanne Kohl

    STZ eyetrial, Germany

    4 publications · 167 citations

    4

    h-index

  2. BW
    Bernd Wissinger

    STZ eyetrial, Germany

    4 publications · 167 citations

    4

    h-index

  3. MS
    Mark S. Springer

    University of California, Riverside, United States

    3 publications · 270 citations

    3

    h-index

  4. CA
    Christopher A. Emerling

    University of California, Riverside, United States

    3 publications · 270 citations

    3

    h-index

  5. ST
    Shoko Tanabe

    Kyoto University, Japan

    2 publications · 58 citations

    2

    h-index

1–5 of 112

Venues

  1. Documenta Ophthalmologica

    4 publications · 137 citations

    4

    h-index

  2. PubMed

    Repository · 3 publications · 181 citations

    3

    h-index

  3. Investigative Ophthalmology & Visual Science

    IOVS · 2 publications · 54 citations

    2

    h-index

  4. The Journal of Physiology

    2 publications · 187 citations

    2

    h-index

  5. Human Mutation

    1 publications · 28 citations

    1

    h-index

1–5