Published in Retina on October 24, 2013
Evaluation of inner retinal layers in eyes with temporal hemianopic visual loss from chiasmal compression using optical coherence tomography. Invest Ophthalmol Vis Sci (2014) 1.01
Poorer neurodevelopmental outcomes associated with cystoid macular edema identified in preterm infants in the intensive care nursery. Ophthalmology (2014) 0.89
Optical coherence tomography reflects brain atrophy in multiple sclerosis: A four-year study. Ann Neurol (2015) 0.88
Microcystic Inner Nuclear Layer Changes and Retinal Nerve Fiber Layer Defects in Eyes with Glaucoma. PLoS One (2015) 0.87
High-resolution en face images of microcystic macular edema in patients with autosomal dominant optic atrophy. Biomed Res Int (2013) 0.86
Inner nuclear layer thickening is inversley proportional to retinal ganglion cell loss in optic neuritis. PLoS One (2013) 0.86
Microcystic changes in the retinal internal nuclear layer associated with optic atrophy: a prospective study. J Ophthalmol (2014) 0.82
The expanding spectrum of aetiologies causing retinal microcystic macular change. Brain (2013) 0.81
Optical coherence tomography shows retinal abnormalities associated with optic nerve disease. Br J Ophthalmol (2014) 0.79
Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements. PLoS One (2015) 0.77
Longitudinal analysis of the structural pattern of pseudophakic cystoid macular edema using multimodal imaging. Graefes Arch Clin Exp Ophthalmol (2015) 0.77
Clinical evaluation of microcystic macular edema in patients with glaucoma. Eye (Lond) (2016) 0.75
Optical coherence tomography findings in methanol toxicity. Int J Retina Vitreous (2017) 0.75
Seven new loci associated with age-related macular degeneration. Nat Genet (2013) 3.81
Interim results from the international trial of Second Sight's visual prosthesis. Ophthalmology (2012) 3.35
Identification and characterization of rod-derived cone viability factor. Nat Genet (2004) 2.63
Using spectral-domain optical coherence tomography imaging to identify the presence of retinal silicone oil emulsification after silicone oil tamponade. Retina (2013) 2.22
Role of hyaluronidase in diplopia after peribulbar anesthesia for cataract surgery. Ophthalmology (2005) 2.10
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2009) 1.93
NMNAT1 mutations cause Leber congenital amaurosis. Nat Genet (2012) 1.86
Panretinal, high-resolution color photography of the mouse fundus. Invest Ophthalmol Vis Sci (2007) 1.82
Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet J Rare Dis (2012) 1.79
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. Hum Mutat (2009) 1.67
Exudative idiopathic polypoidal choroidal vasculopathy and photodynamic therapy with verteporfin. Am J Ophthalmol (2002) 1.61
High resolution fundus imaging by confocal scanning laser ophthalmoscopy in the mouse. Vision Res (2005) 1.59
Ranibizumab versus Bevacizumab for Neovascular Age-related Macular Degeneration: Results from the GEFAL Noninferiority Randomized Trial. Ophthalmology (2013) 1.58
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet J Rare Dis (2011) 1.57
Foveal damage in habitual poppers users. Arch Ophthalmol (2011) 1.56
Poppers-associated retinal toxicity. N Engl J Med (2010) 1.54
Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa. Mol Ther (2009) 1.53
Photodynamic therapy for subfoveal classic choroidal neovascularization related to punctate inner choroidopathy (PIC) or presumed ocular histoplasmosis-like syndrome (POHS-like). Ocul Immunol Inflamm (2006) 1.48
Inherited retinal degenerations: therapeutic prospects. Biol Cell (2004) 1.44
CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice. EMBO Mol Med (2013) 1.42
Successful treatment of idiopathic orbital inflammation with infliximab: an alternative to conventional steroid-sparing agents. Ophthal Plast Reconstr Surg (2008) 1.41
En Face OCT Imaging for the Diagnosis of Outer Retinal Tubulations in Age-Related Macular Degeneration. J Ophthalmol (2012) 1.39
EYS is a major gene for rod-cone dystrophies in France. Hum Mutat (2010) 1.39
Optical coherence tomography findings in tamoxifen retinopathy. Am J Ophthalmol (2005) 1.36
CRB1 mutations in inherited retinal dystrophies. Hum Mutat (2011) 1.34
Foveal shape and structure in a normal population. Invest Ophthalmol Vis Sci (2011) 1.32
Anemia and papilledema. Am J Ophthalmol (2003) 1.27
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2012) 1.25
Anxiety and depression prevalence rates in age-related macular degeneration. Invest Ophthalmol Vis Sci (2007) 1.25
Choroidal infarction following photodynamic therapy with verteporfin. Arch Ophthalmol (2005) 1.22
Rod-derived cone viability factor for treating blinding diseases: from clinic to redox signaling. Sci Transl Med (2010) 1.20
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet (2012) 1.18
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. Hum Mol Genet (2012) 1.18
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. J Cell Biol (2012) 1.16
Retinal degenerations: from cell signaling to cell therapy; pre-clinical and clinical issues. Curr Gene Ther (2007) 1.15
The glutamate transporter EAAT5 works as a presynaptic receptor in mouse rod bipolar cells. J Physiol (2006) 1.15
Genotyping microarray for CSNB-associated genes. Invest Ophthalmol Vis Sci (2009) 1.10
Outer retinal cysts in age-related macular degeneration. Acta Ophthalmol (2011) 1.08
Adaptive optics imaging of geographic atrophy. Invest Ophthalmol Vis Sci (2013) 1.07
Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients. Invest Ophthalmol Vis Sci (2010) 1.05
Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports. BMC Med Genet (2010) 1.03
Retinal-cell-conditioned medium prevents TNF-alpha-induced apoptosis of purified ganglion cells. Invest Ophthalmol Vis Sci (2005) 1.02
Evidence for glutamate-mediated excitotoxic mechanisms during photoreceptor degeneration in the rd1 mouse retina. Mol Vis (2005) 1.01
The aging of the retina. Exp Gerontol (2003) 1.01
Retinal and choroidal changes observed with 'En face' enhanced-depth imaging OCT in central serous chorioretinopathy. Br J Ophthalmol (2013) 0.98
Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations. J Inherit Metab Dis (2010) 0.97
The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina. Hum Mol Genet (2009) 0.97
Mutations in IMPG1 cause vitelliform macular dystrophies. Am J Hum Genet (2013) 0.96
Retinal fluorescein and indocyanine green angiography and spectral-domain optical coherence tomography findings in acute retinal pigment epitheliitis. Retina (2011) 0.95
In vivo observation of the locomotion of microglial cells in the retina. Glia (2010) 0.94
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits. Rejuvenation Res (2007) 0.94
B-scan and "en-face" spectral-domain optical coherence tomography imaging for the diagnosis and followup of acute retinal pigment epitheliitis. Case Rep Med (2013) 0.94
The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes. Biochim Biophys Acta (2008) 0.94
Disease-causing mutations in BEST1 gene are associated with altered sorting of bestrophin-1 protein. Int J Mol Sci (2013) 0.94
PREVALENCE OF RETICULAR PSEUDODRUSEN IN AGE-RELATED MACULAR DEGENERATION USING MULTIMODAL IMAGING. Retina (2016) 0.92
Morphometric analysis of small arteries in the human retina using adaptive optics imaging: relationship with blood pressure and focal vascular changes. J Hypertens (2014) 0.92
Involvement of Pleiotrophin in CNTF-mediated differentiation of the late retinal progenitor cells. Dev Biol (2006) 0.92
AAV-mediated gene delivery in Dp71-null mouse model with compromised barriers. Glia (2013) 0.90
RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlation. Hum Mutat (2011) 0.90
A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family. Mol Vis (2011) 0.90
Association between visual acuity and medical and non-medical costs in patients with wet age-related macular degeneration in France, Germany and Italy. Drugs Aging (2008) 0.90
mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein. RNA (2006) 0.89
Subretinal lymphomatous infiltration in primary intraocular lymphoma revealed by optical coherence tomography. Graefes Arch Clin Exp Ophthalmol (2011) 0.89
Differential proteomic analysis of the mouse retina: the induction of crystallin proteins by retinal degeneration in the rd1 mouse. Mol Cell Proteomics (2003) 0.89
Association between hypovitaminosis D and late stages of age-related macular degeneration: a case-control study. J Am Geriatr Soc (2012) 0.89
High prevalence of IgG4-related lymphoplasmacytic infiltrative disorder in 25 patients with orbital inflammation: a retrospective case series. Br J Ophthalmol (2013) 0.88
Polypoidal choroidal vasculopathy in a patient with angioid streaks secondary to pseudoxanthoma elasticum. Graefes Arch Clin Exp Ophthalmol (2010) 0.88
Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death. PLoS One (2011) 0.88
The cost-effectiveness of the Argus II retinal prosthesis in Retinitis Pigmentosa patients. BMC Ophthalmol (2014) 0.87
Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort. Hum Mutat (2011) 0.87
PromAn: an integrated knowledge-based web server dedicated to promoter analysis. Nucleic Acids Res (2006) 0.87
Cellular localization of the vesicular inhibitory amino acid transporter in the mouse and human retina. J Comp Neurol (2002) 0.87
Optical coherence tomography in tamoxifen retinopathy. Breast Cancer Res Treat (2006) 0.87
Multimodal imaging of white and dark without pressure fundus lesions. Retina (2014) 0.87
Helicobacter pylori and idiopathic central serous chorioretinopathy. Swiss Med Wkly (2004) 0.87
Mammalian retinal horizontal cells are unconventional GABAergic neurons. J Neurochem (2010) 0.86
Neuroglobin involvement in respiratory chain function and retinal ganglion cell integrity. Biochim Biophys Acta (2012) 0.85
Downregulation of apoptosis-inducing factor in Harlequin mice induces progressive and severe optic atrophy which is durably prevented by AAV2-AIF1 gene therapy. Brain (2011) 0.85
Real-time polymerase chain reaction and intraocular antibody production for the diagnosis of viral versus toxoplasmic infectious posterior uveitis. Graefes Arch Clin Exp Ophthalmol (2011) 0.85
Gene therapy in ophthalmology: validation on cultured retinal cells and explants from postmortem human eyes. Hum Gene Ther (2011) 0.84
Transplantation of photoreceptor and total neural retina preserves cone function in P23H rhodopsin transgenic rat. PLoS One (2010) 0.83
Phototoxic action spectrum on a retinal pigment epithelium model of age-related macular degeneration exposed to sunlight normalized conditions. PLoS One (2013) 0.83
Taurine deficiency damages retinal neurones: cone photoreceptors and retinal ganglion cells. Amino Acids (2012) 0.82
℮-conome: an automated tissue counting platform of cone photoreceptors for rodent models of retinitis pigmentosa. BMC Ophthalmol (2011) 0.82
En face spectral domain optical coherence tomography in a case of bilateral acute macular neuroretinopathy. Retina (2015) 0.82
In-vivo accuracy of geometrically correct three-dimensional reconstruction of human coronary arteries: is it influenced by certain parameters? Coron Artery Dis (2006) 0.82
Assessment of visuo-attentional abilities in young children with or without visual disorder: toward a systematic screening in the general population. Res Dev Disabil (2010) 0.82
Spectral domain optical coherence tomography evolutive features in acute macular neuroretinopathy. Eur J Ophthalmol (2012) 0.81
The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins. Neurosci Res (2005) 0.81
Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness. Invest Ophthalmol Vis Sci (2013) 0.81
An unusual retinal phenotype associated with a novel mutation in RHO. Arch Ophthalmol (2010) 0.81
Use of suppression subtractive hybridization to identify genes regulated by ciliary neurotrophic factor in postnatal retinal explants. Mol Vis (2007) 0.81
Flat choroidal nevus inaccessible to ultrasound sonography evaluated by enhanced depth imaging optical coherence tomography. Case Rep Ophthalmol (2011) 0.81
Blindness, weakness, and tingling. Surv Ophthalmol (2012) 0.81
A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina. PLoS One (2013) 0.80