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

Authors

240

  1. SK
    Susanne Kohl

    STZ eyetrial, Germany

    8 publications · 281 citations

    8

    h-index

  2. BW
    Bernd Wissinger

    STZ eyetrial, Germany

    8 publications · 281 citations

    8

    h-index

  3. SG
    Samuel G. Jacobson

    Penn Presbyterian Medical Center, United States

    5 publications · 163 citations

    5

    h-index

  4. MM
    Michel Michaelides

    University College London, United Kingdom

    5 publications · 192 citations

    5

    h-index

  5. AV
    Artur V. Cideciyan

    Penn Presbyterian Medical Center, United States

    4 publications · 94 citations

    4

    h-index

1–5 of 240

Venues

  1. PubMed

    Repository · 5 publications · 385 citations

    5

    h-index

  2. Scientific Reports

    3 publications · 92 citations

    3

    h-index

  3. Archives of Ophthalmology

    2 publications · 93 citations

    2

    h-index

  4. Genomics

    2 publications · 119 citations

    2

    h-index

  5. American Journal of Ophthalmology

    2 publications · 110 citations

    2

    h-index

1–5