List of works - Maureen Neitz

A Color Vision Circuit for Non-Image-Forming Vision in the Primate Retina

scientific article published on 14 February 2020

A multi-stage color model revisited: implications for a gene therapy cure for red-green colorblindness

scientific article

A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect

scientific article

ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY.

scientific article published on 10 July 2015

Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

scientific article

An S-cone circuit for edge detection in the primate retina

scientific article published on 15 August 2019

An adaptation of the Cambridge Colour Test for use with animals

scientific article published on 01 May 2006

An urn model of the development of L/M cone ratios in human and macaque retinas

scientific article

Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease

scientific article

Broad thorny ganglion cells: a candidate for visual pursuit error signaling in the primate retina

scientific article

Changes in the colour of light cue circadian activity.

scientific article published on 18 February 2012

Characterization of a novel form of X-linked incomplete achromatopsia

scientific article

Characterization of opsin gene alleles affecting color vision in a wild population of titi monkeys (Callicebus brunneus).

scientific article

Circuitry to explain how the relative number of L and M cones shapes color experience

scientific article published on June 2016

Color Vision in Aniridia

scientific article published on 01 April 2018

Color Vision: Almost Reason Enough for Having Eyes

article by Jay Neitz et al published 1 January 2001 in Optics and Photonics News

Color perception is mediated by a plastic neural mechanism that is adjustable in adults

scientific article published in August 2002

Color-deficient cone mosaics associated with Xq28 opsin mutations: a stop codon versus gene deletions

scientific article

Colour vision: the wonder of hue.

scientific article published in August 2008

Comparison of the Richmond HRR 4th edition and Farnsworth-Munsell 100 Hue Test for quantitative assessment of tritan color deficiencies

scientific article

Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.

scientific article published on July 2016

Cone photopigment variations in Cebus apella monkeys evidenced by electroretinogram measurements and genetic analysis

scientific article

Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin

scientific article

Cone-isolating ON-OFF electroretinogram for studying chromatic pathways in the retina

scientific article published on April 2014

Curing color blindness--mice and nonhuman primates

scientific article

Deletion of the X-linked opsin gene array locus control region (LCR) results in disruption of the cone mosaic

scientific article

Distinctive receptive field and physiological properties of a wide-field amacrine cell in the macaque monkey retina.

scientific article

Effect of cone spectral topography on chromatic detection sensitivity

scientific article published on 01 April 2020

Effects of Long-Wavelength Lighting on Refractive Development in Infant Rhesus Monkeys

scientific article

Estimates of L:M cone ratio from ERG flicker photometry and genetics

scientific article published in January 2002

Evaluating the human X-chromosome pigment gene promoter sequences as predictors of L:M cone ratio variation

scientific article published on 25 March 2004

Evaluation of an updated HRR color vision test.

scientific article published in May 2004

Expression and Evolution of Short Wavelength Sensitive Opsins in Colugos: A Nocturnal Lineage That Informs Debate on Primate Origins

scientific article (publication date: 2013)

Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness

scholarly article

Gene therapy for red-green colour blindness in adult primates

scientific article

Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies

scientific article published on 06 September 2016

Geographic mapping of choroidal thickness in myopic eyes using 1050-nm spectral domain optical coherence tomography

scientific article

Identification of two novel mutations in families with X-linked ocular albinism

scientific article published on 2 October 2007

Longitudinal evaluation of expression of virally delivered transgenes in gerbil cone photoreceptors

scientific article published on May 2008

Neurobiological hypothesis of color appearance and hue perception

scientific article

Nucleotide polymorphisms upstream of the X-chromosome opsin gene array tune L:M cone ratio

scientific article

Organization of the human trichromatic cone mosaic.

scientific article published in October 2005

PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia

scientific article published on 01 May 2020

Photopigment genes, cones, and color update: disrupting the splicing code causes a diverse array of vision disorders

scientific article published on 19 July 2019

Photopigment optical density of the human foveola and a paradoxical senescent increase outside the fovea

scientific article

Photoreceptor structure and function in patients with congenital achromatopsia.

scientific article

Protanomaly without darkened red is deuteranopia with rods

scientific article published on 18 April 2008

Recombinant adeno-associated virus targets passenger gene expression to cones in primate retina

scientific article published on May 2007

Reconciling Color Vision Models With Midget Ganglion Cell Receptive Fields

scientific article published on 16 August 2019

Residual Cone Structure in Patients With X-Linked Cone Opsin Mutations

scientific article published on 01 August 2018

Rod- and cone-driven responses in mice expressing human L-cone pigment.

scientific article

Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations

scientific article

S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant

scientific article published on January 2014

Specialized synaptic pathway for chromatic signals beneath S-cone photoreceptors is common to human, Old and New World primates.

scientific article

Spectral tuning of ultraviolet cone pigments: an interhelical lock mechanism

scientific article

Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.

scientific article

Synaptic elements for GABAergic feed-forward signaling between HII horizontal cells and blue cone bipolar cells are enriched beneath primate S-cones.

scientific article

The Cone Photoreceptor Mosaic in Aniridia: Within-Family Phenotype-Genotype Discordance

scientific article published on 05 February 2019

The L:M cone ratio in males of African descent with normal color vision

scientific article published on 20 February 2008

The association between L:M cone ratio, cone opsin genes and myopia susceptibility

scientific article published on 11 July 2019

The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.

scientific article published on 05 December 2012

The genetics of New World monkey visual pigments

article

The genetics of normal and defective color vision ⬇️

scientific article published on December 15, 2010

The influence of L-opsin gene polymorphisms and neural ageing on spatio-chromatic contrast sensitivity in 20-71 year olds

scientific article published on 15 September 2015

Topographical cone photopigment gene expression in deutan-type red-green color vision defects

scientific article published in January 2004

Topography of long- and middle-wavelength sensitive cone opsin gene expression in human and Old World monkey retina

scientific article published on 01 May 2006

Topography of the long- to middle-wavelength sensitive cone ratio in the human retina assessed with a wide-field color multifocal electroretinogram

scientific article

Transplantation of Human Embryonic Stem Cell-Derived Retinal Cells into the Subretinal Space of a Non-Human Primate

scientific article

Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency

scientific article published on 01 April 2020

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

scientific article published on 15 February 2013

Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope

scientific article published on May 2004

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene

scientific article published on 18 January 2013

List of works by Maureen Neitz

A Color Vision Circuit for Non-Image-Forming Vision in the Primate Retina

A multi-stage color model revisited: implications for a gene therapy cure for red-green colorblindness

A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect

ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY.

Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

An S-cone circuit for edge detection in the primate retina

An adaptation of the Cambridge Colour Test for use with animals

An urn model of the development of L/M cone ratios in human and macaque retinas

Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease

Broad thorny ganglion cells: a candidate for visual pursuit error signaling in the primate retina

Changes in the colour of light cue circadian activity.

Characterization of a novel form of X-linked incomplete achromatopsia

Characterization of opsin gene alleles affecting color vision in a wild population of titi monkeys (Callicebus brunneus).

Circuitry to explain how the relative number of L and M cones shapes color experience

Color Vision in Aniridia

Color Vision: Almost Reason Enough for Having Eyes

Color perception is mediated by a plastic neural mechanism that is adjustable in adults

Color-deficient cone mosaics associated with Xq28 opsin mutations: a stop codon versus gene deletions

Colour vision: the wonder of hue.

Comparison of the Richmond HRR 4th edition and Farnsworth-Munsell 100 Hue Test for quantitative assessment of tritan color deficiencies

Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.

Cone photopigment variations in Cebus apella monkeys evidenced by electroretinogram measurements and genetic analysis

Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin

Cone-isolating ON-OFF electroretinogram for studying chromatic pathways in the retina

Curing color blindness--mice and nonhuman primates

Deletion of the X-linked opsin gene array locus control region (LCR) results in disruption of the cone mosaic

Distinctive receptive field and physiological properties of a wide-field amacrine cell in the macaque monkey retina.

Effect of cone spectral topography on chromatic detection sensitivity

Effects of Long-Wavelength Lighting on Refractive Development in Infant Rhesus Monkeys

Estimates of L:M cone ratio from ERG flicker photometry and genetics

Evaluating the human X-chromosome pigment gene promoter sequences as predictors of L:M cone ratio variation

Evaluation of an updated HRR color vision test.

Expression and Evolution of Short Wavelength Sensitive Opsins in Colugos: A Nocturnal Lineage That Informs Debate on Primate Origins

Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness

Gene therapy for red-green colour blindness in adult primates

Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies

Geographic mapping of choroidal thickness in myopic eyes using 1050-nm spectral domain optical coherence tomography

Identification of two novel mutations in families with X-linked ocular albinism

Longitudinal evaluation of expression of virally delivered transgenes in gerbil cone photoreceptors

Neurobiological hypothesis of color appearance and hue perception

Nucleotide polymorphisms upstream of the X-chromosome opsin gene array tune L:M cone ratio

Organization of the human trichromatic cone mosaic.

PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia

Photopigment genes, cones, and color update: disrupting the splicing code causes a diverse array of vision disorders

Photopigment optical density of the human foveola and a paradoxical senescent increase outside the fovea

Photoreceptor structure and function in patients with congenital achromatopsia.

Protanomaly without darkened red is deuteranopia with rods

Recombinant adeno-associated virus targets passenger gene expression to cones in primate retina

Reconciling Color Vision Models With Midget Ganglion Cell Receptive Fields

Residual Cone Structure in Patients With X-Linked Cone Opsin Mutations

Rod- and cone-driven responses in mice expressing human L-cone pigment.

Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations

S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant

Specialized synaptic pathway for chromatic signals beneath S-cone photoreceptors is common to human, Old and New World primates.

Spectral tuning of ultraviolet cone pigments: an interhelical lock mechanism

Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.

Synaptic elements for GABAergic feed-forward signaling between HII horizontal cells and blue cone bipolar cells are enriched beneath primate S-cones.

The Cone Photoreceptor Mosaic in Aniridia: Within-Family Phenotype-Genotype Discordance

The L:M cone ratio in males of African descent with normal color vision

The association between L:M cone ratio, cone opsin genes and myopia susceptibility

The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.

The genetics of New World monkey visual pigments

The genetics of normal and defective color vision ⬇️

The influence of L-opsin gene polymorphisms and neural ageing on spatio-chromatic contrast sensitivity in 20-71 year olds

Topographical cone photopigment gene expression in deutan-type red-green color vision defects

Topography of long- and middle-wavelength sensitive cone opsin gene expression in human and Old World monkey retina

Topography of the long- to middle-wavelength sensitive cone ratio in the human retina assessed with a wide-field color multifocal electroretinogram

Transplantation of Human Embryonic Stem Cell-Derived Retinal Cells into the Subretinal Space of a Non-Human Primate

Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene