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Select item 102883241.

Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations

Giuseppe Giovanni Nardone, Beatrice Spedicati, Maria Pina Concas, Aurora Santin, Anna Morgan, Lorenzo Mazzetto, Maurizio Battaglia-Parodi, Giorgia Girotto

Front Genet. 2023; 14: 1161696. Published online 2023 Jun 9. doi: 10.3389/fgene.2023.1161696

PMCID:: PMC10288324

Abstract Article PDF–1.1M

Select item 102383962.

The causal mutation in ARR3 gene for high myopia and progressive color vision defect

Lei Gu, Peikuan Cong, Qingyao Ning, Bo Jiang, Jianyong Wang, Hongguang Cui

Sci Rep. 2023; 13: 8986. Published online 2023 Jun 2. doi: 10.1038/s41598-023-36141-0

PMCID:: PMC10238396

Abstract Article PDF–1.6M

Select item 94809883.

High visibility colored fabrics for normal trichromats and individuals with color vision defects in a sunset-simulated environment

Tatsuya Iizuka, Takushi Kawamorita, Hajime Tsuji, Hiroyuki Kanai, Toshihiro Hirai, Hiroo Suzuki, Tomoya Handa, Hitoshi Ishikawa

PLoS One. 2022; 17(9): e0274824. Published online 2022 Sep 16. doi: 10.1371/journal.pone.0274824

PMCID:: PMC9480988

Abstract Article PDF–2.3M

Select item 89913854.

A Novel Smartphone-Based Color Test for Detection of Color Vision Defects in Age Related Macular Degeneration

Vassilios Karampatakis, Diamantis Almaliotis, Leonidas Karamitopoulos, George Kalliris, Stavroula Almpanidou

J Ophthalmol. 2022; 2022: 9744065. Published online 2022 Mar 31. doi: 10.1155/2022/9744065

PMCID:: PMC8991385

Abstract Article PDF–913K

Select item 82127665.

A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect

Susanne Kohl, Pablo Llavona, Alexandra Sauer, Peggy Reuter, Nicole Weisschuh, Melanie Kempf, Florian Alexander Dehmelt, Aristides B Arrenberg, Ieva Sliesoraityte, Eberhart Zrenner, Mary J van Schooneveld, Günther Rudolph, Laura Kühlewein, Bernd Wissinger

Hum Mol Genet. 2021 Jul 1; 30(13): 1218–1229. Published online 2021 Apr 22. doi: 10.1093/hmg/ddab117

PMCID:: PMC8212766

Abstract Article PDF–1.0M

Select item 67883156.

Prevalence and Determinants of Color Vision Defects among Preparatory University Students at Makkah, Saudi Arabia

Osama Abdulqadir Khairoalsindi, Bayan Mutlaq Almasoudi, Ashjan Yousef Bamahfouz, Abdullah Atiah Alghamdi, Muhammad Irfanullah Siddiqui

Middle East Afr J Ophthalmol. 2019 Jul-Sep; 26(3): 133–137. Published online 2019 Sep 30. doi: 10.4103/meajo.MEAJO_29_19

PMCID:: PMC6788315

Abstract Article

Select item 66981627.

Impact of congenital color vision defect on color-related tasks among schoolchildren in Durban, South Africa

Khathutshelo Percy Mashige

Clin Optom (Auckl) 2019; 11: 97–102. Published online 2019 Aug 13. doi: 10.2147/OPTO.S204332

PMCID:: PMC6698162

Abstract Article PDF–277K

Select item 48875818.

Acquired Color Vision Defects and Hexane Exposure: A Study of San Francisco Bay Area Automotive Mechanics

Stella Beckman, Ellen A. Eisen, Michael N. Bates, Sa Liu, Gunilla Haegerstrom-Portnoy, S. Katharine Hammond

Am J Epidemiol. 2016 Jun 1; 183(11): 969–976. Published online 2016 May 17. doi: 10.1093/aje/kwv328

PMCID:: PMC4887581

Abstract Article PDF–123K

Select item 48744519.

Diagnosis of Normal and Abnormal Color Vision with Cone-Specific VEPs

Jeff C. Rabin, Andrew C. Kryder, Dan Lam

Transl Vis Sci Technol. 2016 May; 5(3): 8. Published online 2016 May 17. doi: 10.1167/tvst.5.3.8

PMCID:: PMC4874451

Abstract Article PDF–831K

Select item 359563210.

Prevalence of Red-Green Color Vision Defects among Muslim Males and Females of Manipur, India

Ahsana SHAH, Ruqaiya HUSSAIN, Mohd FAREED, Mohammad AFZAL

Iran J Public Health. 2013; 42(1): 16–24. Published online 2013 Jan 1.

PMCID:: PMC3595632

Abstract Article PDF–380K

Select item 186016311.

Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case‐control study

P A Quiros, R J Torres, S Salomao, A Berezovsky, V Carelli, J Sherman, F Sadun, A De Negri, R Belfort, A A Sadun

Br J Ophthalmol. 2006 Feb; 90(2): 150–153. doi: 10.1136/bjo.2005.074526

PMCID:: PMC1860163

Abstract Article PDF–125K

Select item 172058712.

Impact of congenital colour vision defects on occupation

P Cumberland, J Rahi, C Peckham

Arch Dis Child. 2005 Sep; 90(9): 906–908. Published online 2005 May 24. doi: 10.1136/adc.2004.062067

PMCID:: PMC1720587

Summary PDF–56K

Select item 171566213.

Color vision defects in adrenomyeloneuropathy.

G H Sack, Jr, M B Raven, H W Moser

Am J Hum Genet. 1989 Jun; 44(6): 794–798.

PMCID:: PMC1715662

Summary Page Browse PDF–793K

Select item 171554514.

Molecular basis of abnormal red-green color vision: a family with three types of color vision defects.

M Drummond-Borg, S Deeb, A G Motulsky

Am J Hum Genet. 1988 Nov; 43(5): 675–683.

PMCID:: PMC1715545

Summary Page Browse PDF–1.3M

Select item 168281215.

Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.

S S Deeb, D T Lindsey, Y Hibiya, E Sanocki, J Winderickx, D Y Teller, A G Motulsky

Am J Hum Genet. 1992 Oct; 51(4): 687–700.

PMCID:: PMC1682812

Summary Page Browse PDF–2.2M

Select item 128358216.

Cone pigments in human deutan colour vision defects.

M Alpern, T Wake

J Physiol. 1977 Apr; 266(3): 595–612. doi: 10.1113/jphysiol.1977.sp011784

PMCID:: PMC1283582

Summary Page Browse PDF–1.8M

Select item 989686717.

Color Vision in Blue Cone Monochromacy: Outcome Measures for a Clinical Trial

Abraham A. Mascio, Alejandro J. Roman, Artur V. Cideciyan, Rebecca Sheplock, Vivian Wu, Alexandra V. Garafalo, Alexander Sumaroka, Sydney Pirkle, Susanne Kohl, Bernd Wissinger, Samuel G. Jacobson, John L. Barbur

Transl Vis Sci Technol. 2023 Jan; 12(1): 25. Published online 2023 Jan 24. doi: 10.1167/tvst.12.1.25

PMCID:: PMC9896867

Abstract Article PDF–3.1M

Select item 922473918.

Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

Katarina Stingl, Britta Baumann, Pietro De Angeli, Ajoy Vincent, Elise Héon, Monique Cordonnier, Elfriede De Baere, Salmo Raskin, Mario Teruo Sato, Naoye Shiokawa, Susanne Kohl, Bernd Wissinger

Int J Mol Sci. 2022 Jun; 23(12): 6868. Published online 2022 Jun 20. doi: 10.3390/ijms23126868

PMCID:: PMC9224739

Abstract Article PDF–1.7M

Select item 860560119.

Identification of a novel RPGR mutation associated with X-linked cone-rod dystrophy in a Chinese family

Yafang Wang, Shu Liu, Yuanqi Zhai, Yang Liu, Xiaoling Wan, Wenqiu Wang, Fenghua Wang, Xiaodong Sun

BMC Ophthalmol. 2021; 21: 401. Published online 2021 Nov 20. doi: 10.1186/s12886-021-02166-0

PMCID:: PMC8605601

Abstract Article PDF–1.5M

Select item 799618020.

Optic Atrophy and Inner Retinal Thinning in CACNA1F-Related Congenital Stationary Night Blindness

Kate E Leahy, Tom Wright, Monika K Grudzinska Pechhacker, Isabelle Audo, Anupreet Tumber, Erika Tavares, Heather MacDonald, Jeff Locke, Cynthia VandenHoven, Christina Zeitz, Elise Heon, J Raymond Buncic, Ajoy Vincent

Genes (Basel) 2021 Mar; 12(3): 330. Published online 2021 Feb 25. doi: 10.3390/genes12030330