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2021 18
2022 26
2023 17
2024 10
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Achromatopsia: Genetics and Gene Therapy.
Michalakis S, Gerhardt M, Rudolph G, Priglinger S, Priglinger C. Michalakis S, et al. Mol Diagn Ther. 2022 Jan;26(1):51-59. doi: 10.1007/s40291-021-00565-z. Epub 2021 Dec 3. Mol Diagn Ther. 2022. PMID: 34860352 Free PMC article. Review.
Achromatopsia (ACHM), also known as rod monochromatism or total color blindness, is an autosomal recessively inherited retinal disorder that affects the cones of the retina, the type of photoreceptors responsible for high-acuity daylight vision. ...
Achromatopsia (ACHM), also known as rod monochromatism or total color blindness, is an autosomal recessively inherited retinal …
Blue Cone Monochromatism.
Hartung KJ, Tsang SH, Sharma T, Diaconita V. Hartung KJ, et al. Adv Exp Med Biol. 2025;1467:73-75. doi: 10.1007/978-3-031-72230-1_14. Adv Exp Med Biol. 2025. PMID: 40736816 Review.
Color vision in civil aviation.
Singh AK, Khan MA, Singh A, Maheshwari A. Singh AK, et al. Indian J Ophthalmol. 2021 May;69(5):1032-1037. doi: 10.4103/ijo.IJO_2252_20. Indian J Ophthalmol. 2021. PMID: 33913828 Free PMC article. Review.
Color vision deficiency (CVD) is a condition that results in individuals being unable to distinguish differences between certain colors. ...
Color vision deficiency (CVD) is a condition that results in individuals being unable to distinguish differences betwee
Gene therapy in color vision deficiency: a review.
El Moussawi Z, Boueiri M, Al-Haddad C. El Moussawi Z, et al. Int Ophthalmol. 2021 May;41(5):1917-1927. doi: 10.1007/s10792-021-01717-0. Epub 2021 Feb 2. Int Ophthalmol. 2021. PMID: 33528822 Review.
BACKGROUND: Color vision deficiencies are a group of vision disorders, characterized by abnormal color discrimination. They include red-green color blindness, yellow-blue color blindness and achromatopsia, among others. The deficiencies are caused by m …
BACKGROUND: Color vision deficiencies are a group of vision disorders, characterized by abnormal color discrimination. They include red-gree …
Color Vision Deficiency Survey in Anatomic Pathology.
Flotte TJ, Cornell LD. Flotte TJ, et al. Am J Clin Pathol. 2022 Oct 6;158(4):516-520. doi: 10.1093/ajcp/aqac081. Am J Clin Pathol. 2022. PMID: 35913114
Twenty-three people, all men, identified themselves as color vision deficient, with 22 reporting red-green color vision deficiency and 1 reporting uncertain type. Eight pathologists and cytotechnologists indicated that they thought that their color
Twenty-three people, all men, identified themselves as color vision deficient, with 22 reporting red-green color vision def
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.
Wang Y, Sun W, Xiao X, Jiang Y, Ouyang J, Wang J, Yi Z, Li S, Jia X, Wang P, Hejtmancik JF, Zhang Q. Wang Y, et al. Invest Ophthalmol Vis Sci. 2023 Apr 3;64(4):29. doi: 10.1167/iovs.64.4.29. Invest Ophthalmol Vis Sci. 2023. PMID: 37097228 Free PMC article.
PURPOSE: Specific haplotypes (LVAVA, LIVVA, and LIAVA) formed by five polymorphisms (p.L153M, p.V171I, p.A174V, p.I178V, and p.S180A in exon 3 of OPN1LW) that cause partial or complete exon skipping have been reported as unique genetic causes of high myopia with or without col
PURPOSE: Specific haplotypes (LVAVA, LIVVA, and LIAVA) formed by five polymorphisms (p.L153M, p.V171I, p.A174V, p.I178V, and p.S180A in exon …
Refractive errors among commercial drivers.
Kumar M, Mahaseth A, Parveen S, Rafeeq U, Chauhan L. Kumar M, et al. Indian J Ophthalmol. 2022 Jun;70(6):2112-2116. doi: 10.4103/ijo.IJO_2510_21. Indian J Ophthalmol. 2022. PMID: 35647994 Free PMC article.
Dry eye was reported in 70 (24.9%), stereo deficiency in 77 (27.4%), and color vision deficiency in 11 (3.9%) drivers. Three drivers were diagnosed with cataract, and two were referred for retina evaluation. CONCLUSION: Hyperopia in both eyes was the most com …
Dry eye was reported in 70 (24.9%), stereo deficiency in 77 (27.4%), and color vision deficiency in 11 (3.9%) drivers. …
Global Prevalence of Congenital Color Vision Deficiency among Children and Adolescents, 1932-2022.
Jeong YD, Cho J, Son Y, Jo Y, Yim Y, Kim TH, Kim S, Cho H, Rahmati M, Smith L, Woo HG, Kim JH, Kim YJ, Yang JM, Yon DK. Jeong YD, et al. Ophthalmology. 2025 Dec;132(12):1431-1444. doi: 10.1016/j.ophtha.2025.07.031. Epub 2025 Aug 5. Ophthalmology. 2025. PMID: 40769301
PURPOSE: To estimate the prevalence of congenital color vision deficiency (CVD), categorized by geographical region, ethnicity, type (deutan, protan, and tritan), and severity (anomalous trichromacy, dichromacy, and monochromacy). ...
PURPOSE: To estimate the prevalence of congenital color vision deficiency (CVD), categorized by geographical region, et …
Prevalence of color vision deficiency in Africa: Systematic review and meta-analysis.
Tilahun MM, Sema FD, Mengistie BA, Abdulkadir NH, Jara AG. Tilahun MM, et al. PLoS One. 2024 Dec 4;19(12):e0313819. doi: 10.1371/journal.pone.0313819. eCollection 2024. PLoS One. 2024. PMID: 39630815 Free PMC article.
BACKGROUND: Color vision deficiency (CVD) cause is the difficulty distinguishing colors, which can present vocational and avocational challenges. ...A funnel plot showed that all of the studies were symmetric, and the Egger test showed no publication bias. CO …
BACKGROUND: Color vision deficiency (CVD) cause is the difficulty distinguishing colors, which can present vocational a …
Color Vision Testing, Standards, and Visual Performance of the U.S. Military.
Gao H, Kirkendall CD, Kinney MJ, Preston AM, Reddix MD. Gao H, et al. Mil Med. 2023 Jan 4;188(1-2):49-57. doi: 10.1093/milmed/usac080. Mil Med. 2023. PMID: 35352814
INTRODUCTION: Color vision deficiency (CVD) is a disqualifying condition for military special duty occupations. ...
INTRODUCTION: Color vision deficiency (CVD) is a disqualifying condition for military special duty occupations. ...
87 results