The cone dysfunction syndromes: Table 1

Causes and consequences of inherited cone disorders

(2014) Susanne Roosing et al.   PROGRESS IN RETINAL AND EYE RESEARCH

A comparison of the causes of blindness certifications in England and Wales in working age adults (16–64 years), 1999–2000 with 2009–2010

(2014) Gerald Liew et al.   BMJ Open

Spectral-Domain Optical Coherence Tomography Staging and Autofluorescence Imaging in Achromatopsia

(2014) Jonathan P. Greenberg et al.   JAMA Ophthalmology

Diagnostic Fundus Autofluorescence Patterns in Achromatopsia

(2013) Abigail T. Fahim et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

Human Cone Visual Pigment Deletions Spare Sufficient Photoreceptors to Warrant Gene Therapy

(2013) Artur V. Cideciyan et al.   HUMAN GENE THERAPY

Gene therapy clinical trials worldwide to 2012 - an update

(2013) Samantha L. Ginn et al.   JOURNAL OF GENE MEDICINE

Retinal Structure and Function in Achromatopsia

(2013) Venki Sundaram et al.   OPHTHALMOLOGY

Distinct and Atypical Intrinsic and Extrinsic Cell Death Pathways between Photoreceptor Cell Types upon Specific Ablation of Ranbp2 in Cone Photoreceptors

(2013) Kyoung-in Cho et al.   PLoS Genetics

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

(2012) Susanne Kohl et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect

(2012) Hisao Ueyama et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia

(2012) Mervyn George Thomas et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

(2011) L. S. Carvalho et al.   HUMAN MOLECULAR GENETICS

Oligocone trichromacy is part of the spectrum ofCNGA3-related cone system disorders

(2011) Ajoy Vincent et al.   OPHTHALMIC GENETICS

High-Resolution In Vivo Imaging in Achromatopsia

(2011) Mervyn G. Thomas et al.   OPHTHALMOLOGY

CNTF and retina

(2011) Rong Wen et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Noninvasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope

(2011) Alfredo Dubra et al.   Biomedical Optics Express

X-linked myopia: Bornholm Eye Disease

(2010) Marianne Schwartz et al.   CLINICAL GENETICS

Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia

(2010) Tanja Grau et al.   HUMAN MOLECULAR GENETICS

Gene therapy rescues cone function in congenital achromatopsia

(2010) András M. Komáromy et al.   HUMAN MOLECULAR GENETICS

Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

(2010) Stylianos Michalakis et al.   MOLECULAR THERAPY

X-linked myopia in danish family

(2009) M. Haim et al.   ACTA OPHTHALMOLOGICA

Electroretinograms in patients with achromatopsia

(2009) Sten Andréasson et al.   ACTA OPHTHALMOLOGICA

Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders

(2009) Alberta A.H.J. Thiadens et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Gene therapy for red–green colour blindness in adult primates

(2009) Katherine Mancuso et al.   NATURE

Genetic Etiology and Clinical Consequences of Complete and Incomplete Achromatopsia

(2009) Alberta A.H.J. Thiadens et al.   OPHTHALMOLOGY

Novel Mutations and Electrophysiologic Findings in RGS9- and R9AP-Associated Retinal Dysfunction (Bradyopsia)

(2009) Michel Michaelides et al.   OPHTHALMOLOGY

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

(2009) B. Chang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia

(2008) Peggy Reuter et al.   HUMAN MUTATION

In vivo imaging of the photoreceptor mosaic of a rod monochromat

(2008) Joseph Carroll et al.   VISION RESEARCH