Gerald Allen Fishman
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(Suggest an Edit or Addition)Gerald Allen Fishman's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics (2008) (687)
- Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years. (2012) (598)
- Rhodopsin mutations in autosomal dominant retinitis pigmentosa. (1991) (482)
- Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. (1998) (465)
- Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate (2000) (463)
- Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness (1998) (447)
- Multiple evanescent white dot syndrome. I. Clinical findings. (1984) (330)
- In vivo imaging of human cone photoreceptor inner segments. (2014) (303)
- Mutations in the Cone-Rod Homeobox Gene Are Associated with the Cone-Rod Dystrophy Photoreceptor Degeneration (1997) (261)
- Mutations in the CRB1 gene cause Leber congenital amaurosis. (2001) (236)
- Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. (1990) (236)
- Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. (2005) (232)
- A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. (2002) (229)
- An analysis of allelic variation in the ABCA4 gene. (2001) (210)
- iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration. (2013) (207)
- Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene. (1999) (206)
- Fundus flavimaculatus. A clinical classification. (1976) (206)
- Retinitis pigmentosa. Genetic percentages. (1978) (199)
- Visual acuity loss and clinical observations in a large series of patients with Stargardt disease. (2003) (196)
- Acetazolamide for treatment of chronic macular edema in retinitis pigmentosa. (1989) (195)
- Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older. (1999) (192)
- Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration (2012) (178)
- 'On' response defect in paraneoplastic night blindness with cutaneous malignant melanoma. (1992) (168)
- Mutation analysis of 3 genes in patients with Leber congenital amaurosis. (2000) (166)
- Histopathologic findings in Best's vitelliform macular dystrophy. (1988) (163)
- Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease (2013) (160)
- Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis. (1987) (152)
- Allelic variation in the VMD2 gene in best disease and age-related macular degeneration. (2000) (152)
- Photoreceptor structure and function in patients with congenital achromatopsia. (2011) (145)
- Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis. (1991) (145)
- Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing (2013) (143)
- Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia (2002) (140)
- Rate of visual field loss in retinitis pigmentosa. (1997) (136)
- Topical dorzolamide for the treatment of cystoid macular edema in patients with retinitis pigmentosa. (2006) (136)
- Analysis of the ABCA4 gene by next-generation sequencing. (2011) (134)
- The prevalence of cystoid macular oedema in retinitis pigmentosa patients determined by optical coherence tomography (2008) (132)
- Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa. (2000) (131)
- Macular lesions associated with retinitis pigmentosa. (1977) (128)
- Visual acuity loss in patients with Stargardt's macular dystrophy. (1987) (127)
- X-linked retinitis pigmentosa. Profile of clinical findings. (1988) (125)
- Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. (1998) (124)
- Abnormal sperm and photoreceptor axonemes in Usher's syndrome. (1986) (122)
- Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration (2017) (121)
- Multiple evanescent white dot syndrome. II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease. (1984) (121)
- Patterns of visual field progression in patients with retinitis pigmentosa. (1998) (121)
- Eye-movement training for reading in patients with age-related macular degeneration. (2005) (120)
- Analysis of the ABCA4 genomic locus in Stargardt disease. (2014) (118)
- Retinitis pigmentosa. A symposium on terminology and methods of examination. (1983) (114)
- Autosomal dominant retinitis pigmentosa. A method of classification. (1985) (113)
- Perceived and actual performance of daily tasks: relationship to visual function tests in individuals with retinitis pigmentosa. (2001) (112)
- Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families. (1990) (111)
- Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa. (2010) (111)
- Human macular pigment assessed by imaging fundus reflectometry (1989) (107)
- Electrophysiologic Testing in Disorders of the Retina, Optic Nerve and Visual Pathway (1990) (106)
- Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa. (1992) (106)
- EFFICACY OF DORZOLAMIDE HYDROCHLORIDE IN THE MANAGEMENT OF CHRONIC CYSTOID MACULAR EDEMA IN PATIENTS WITH RETINITIS PIGMENTOSA (1997) (105)
- AUTOIMMUNE RETINOPATHY AND ANTIRETINAL ANTIBODIES: A REVIEW (2014) (105)
- X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers. (1986) (105)
- Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene. (1991) (103)
- BBS genotype–phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition (2011) (103)
- Natural History of Phenotypic Changes in Stargardt Macular Dystrophy (2009) (103)
- Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. (2012) (101)
- Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa. (1985) (101)
- Variability of visual field measurements in normal subjects and patients with retinitis pigmentosa. (1984) (100)
- Foveal lesions seen in retinitis pigmentosa. (1977) (99)
- Assessment of driving performance in patients with retinitis pigmentosa. (1992) (98)
- Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa. (1997) (97)
- The luminance-response function of the dark-adapted human electroretinogram (1989) (94)
- Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosis. (2010) (94)
- North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13. (2016) (94)
- ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophy. (2003) (94)
- Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa. (1991) (93)
- Relationship between difficulty in performing daily activities and clinical measures of visual function in patients with retinitis pigmentosa. (1997) (93)
- USE OF DORZOLAMIDE FOR PATIENTS WITH X-LINKED RETINOSCHISIS (2006) (91)
- A comparison of driving in older subjects with and without age-related macular degeneration. (1995) (90)
- Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa. (1992) (89)
- Refractive errors of retinitis pigmentosa patients. (1978) (88)
- CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy. (2009) (86)
- Visual acuity in patients with best vitelliform macular dystrophy. (1993) (85)
- EVALUATION OF GENOTYPE–PHENOTYPE ASSOCIATIONS IN LEBER CONGENITAL AMAUROSIS (2005) (84)
- Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population (2010) (83)
- Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene. (2012) (83)
- Clinical subtypes of cone-rod dystrophy. (1993) (82)
- Acquired color vision defects. (1971) (81)
- Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia (2016) (81)
- The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic. (2012) (80)
- AUTOSOMAL RECESSIVE VITELLIFORM MACULAR DYSTROPHY IN A LARGE COHORT OF VITELLIFORM MACULAR DYSTROPHY PATIENTS (2011) (78)
- Cone-rod dystrophy. A clinical and histopathologic report. (1986) (78)
- Diagnostic features of the Favre-Goldmann syndrome. (1976) (77)
- Prolonged rod dark adaptation in retinitis pigmentosa. (1984) (77)
- Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays. (2007) (76)
- Correlation of optical coherence tomography findings with visual acuity and macular lesions in patients with X-linked retinoschisis. (2005) (75)
- Delayed rod dark adaptation in patients with Stargardt's disease. (1991) (75)
- Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa. (1992) (74)
- Efficacy of sustained topical dorzolamide therapy for cystic macular lesions in patients with retinitis pigmentosa and usher syndrome. (2010) (73)
- Retinal nerve fiber layer defects in RP patients. (2007) (73)
- Efficacy of sustained topical dorzolamide therapy for cystic macular lesions in patients with X-linked retinoschisis. (2010) (72)
- Rod-cone interaction in flicker perimetry. (1984) (71)
- Properties of the human cone system electroretinogram during light adaptation. (1989) (69)
- Vitreous fluorophotometry in patients with retinitis pigmentosa. (1981) (69)
- Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health. (2014) (68)
- A genetic analysis of retinitis pigmentosa. (1983) (68)
- Evaluation of driving performance in patients with juvenile macular dystrophies. (1993) (68)
- Retinitis pigmentosa. Visual loss. (1978) (67)
- Monitoring cystoid macular edema by optical coherence tomography in patients with retinitis pigmentosa. (2004) (67)
- Autosomal dominant vitreoretinochoroidopathy. (1982) (67)
- Visual acuity impairment in patients with retinitis pigmentosa. (1996) (67)
- Autoantibodies in Melanoma-Associated Retinopathy Target TRPM1 Cation Channels of Retinal ON Bipolar Cells (2011) (66)
- Continued use of dorzolamide for the treatment of cystoid macular oedema in patients with retinitis pigmentosa (2007) (66)
- Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome. (2011) (65)
- The prevalence of cystoid macular oedema on optical coherence tomography in retinitis pigmentosa patients without cystic changes on fundus examination (2009) (65)
- Driving performance of retinitis pigmentosa patients. (1981) (63)
- Rod and cone dysfunction in carriers of X-linked retinitis pigmentosa. (1988) (62)
- Inherited and Environmentally Induced Retinal Degenerations (1990) (62)
- Retinal nerve fiber layer analysis in RP patients using Fourier-domain OCT. (2008) (61)
- NATURAL COURSE OF VISUAL FIELD LOSS IN PATIENTS WITH TYPE 2 USHER SYNDROME (2007) (61)
- Abnormal plasma levels of polyunsaturated fatty acid in autosomal dominant retinitis pigmentosa. (1987) (60)
- Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease. (2012) (59)
- Structural and functional correlation in sickle cell retinopathy using spectral-domain optical coherence tomography and scanning laser ophthalmoscope microperimetry. (2011) (58)
- Supernormal scotopic ERG in cone dystrophy. (1984) (58)
- Rod and cone system contributions to oscillatory potentials: An explanation for the conditioning flash effect (1987) (58)
- FUNDUS FINDINGS AND LONGITUDINAL STUDY OF VISUAL ACUITY LOSS IN PATIENTS WITH X-LINKED RETINOSCHISIS (2004) (57)
- THE USE OF CARBONIC ANHYDRASE INHIBITORS IN THE RETREATMENT OF CYSTIC MACULAR LESIONS IN RETINITIS PIGMENTOSA AND X-LINKED RETINOSCHISIS (2011) (57)
- Principles of Medical Genetics (1992) (57)
- Visual acuity loss in patients with Usher's syndrome. (1986) (56)
- Treatment of cystic macular lesions in hereditary retinal dystrophies. (2013) (55)
- Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. (2014) (55)
- REBOUND OF CYSTOID MACULAR EDEMA WITH CONTINUED USE OF ACETAZOLAMIDE IN PATIENTS WITH RETINITIS PIGMENTOSA (2005) (54)
- Extremely hypomorphic and severe deep intronic variants in the ABCA4 locus result in varying Stargardt disease phenotypes (2018) (54)
- Multimodal Imaging of Photoreceptor Structure in Choroideremia (2016) (54)
- Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT) (2015) (54)
- Variability of full-field electroretinogram responses in subjects without diffuse photoreceptor cell disease. (2003) (54)
- Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex. (1994) (53)
- Visual acuity and visual field impairment in Usher syndrome. (1998) (53)
- Determination of human cone pigment density difference spectra in spatially resolved regions of the fovea (1983) (53)
- Retinal findings in melanoma-associated retinopathy. (2001) (52)
- The natural history of stargardt disease with specific sequence mutation in the ABCA4 gene. (2009) (52)
- Relation of response to treatment with dorzolamide in X-linked retinoschisis to the mechanism of functional loss in retinoschisin. (2009) (52)
- Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene. (2008) (50)
- Vestibular and Auditory Function in Usher's Syndrome (1984) (50)
- Difficulty in performing everyday activities in patients with juvenile macular dystrophies: comparison with patients with retinitis pigmentosa (1998) (50)
- Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change (1999) (50)
- Effect of methazolamide on chronic macular edema in patients with retinitis pigmentosa. (1994) (49)
- Mutations in the RPE 65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis (1998) (48)
- Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype. (1985) (48)
- REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA (2017) (48)
- Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290. (2013) (46)
- Detection using the multifocal electroretinogram of mosaic retinal dysfunction in carriers of X-linked retinitis pigmentosa. (2002) (46)
- Inherited macular dystrophies: a clinical overview. (1990) (46)
- Frequency of optic disc or parapapillary nerve fiber layer drusen in retinitis pigmentosa. (1997) (46)
- Contrast sensitivity in retinitis pigmentosa. (1981) (46)
- A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa. (2000) (45)
- Light adaptation, rods, and the human cone flicker ERG (1992) (44)
- Ophthalmic Molecular Genetics (2004) (44)
- Spectral-Domain Optical Coherence Tomography and Fundus Autofluorescence Characteristics in Patients with Fundus Albipunctatus and Retinitis Punctata Albescens (2010) (44)
- Ocular phototoxicity: guidelines for selecting sunglasses. (1986) (44)
- Predicting the pathogenicity of RPE65 mutations (2009) (44)
- Cystic macular oedema on spectral-domain optical coherence tomography in choroideremia patients without cystic changes on fundus examination (2011) (44)
- Contrast sensitivity deficits in inferred magnocellular and parvocellular pathways in retinitis pigmentosa. (2004) (43)
- CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosis. (2009) (43)
- Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes. (2004) (43)
- Pseudovitelliform macular degeneration. (1977) (42)
- Acute macular neuroretinopathy: early receptor potential change suggests photoreceptor pathology. (1984) (42)
- Clinical phenotypes in carriers of Leber congenital amaurosis mutations. (2005) (42)
- Contrast thresholds for letter identification in retinitis pigmentosa. (1992) (42)
- TOPICAL DORZOLAMIDE FOR TREATMENT OF CYSTOID MACULAR EDEMA IN PATIENTS WITH CHOROIDEREMIA (2012) (41)
- Intraocular Light Scatter in Patients with Retinitis Pigmentosa (1996) (41)
- Color matches of patients with retinitis pigmentosa. (1980) (41)
- On-response deficit in the electroretinogram of the cone system in X-linked retinoschisis. (2001) (41)
- Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene. (2017) (41)
- Genetic and Clinical Analysis of ABCA4-Associated Disease in African American Patients (2014) (40)
- Localized retinal dysfunction in central serous chorioretinopathy as measured using the multifocal electroretinogram. (2002) (40)
- OUTCOME MEASURES AND THEIR APPLICATION IN CLINICAL TRIALS FOR RETINAL DEGENERATIVE DISEASES: Outline, Review, and Perspective (2005) (40)
- How strong is the evidence that nutritional supplements slow the progression of retinitis pigmentosa? (2010) (39)
- CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis. (2006) (39)
- Novel frameshift mutations in CRX associated with Leber congenital amaurosis (2001) (39)
- A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction. (2002) (39)
- Visual acuity vs letter contrast sensitivity in retinitis pigmentosa (1995) (39)
- Short-term inter-visit variability of erg amplitudes in normal subjects and patients with retinitis pigmentosa. (2005) (38)
- X-linked recessive retinitis pigmentosa and vitreous fluorophotometry. A study of female heterozygotes. (1980) (38)
- Chorioretinal Lesions in a Case of Melanoma-Associated Retinopathy Treated With Pembrolizumab. (2016) (38)
- Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23. (2003) (38)
- Autosomal dominant vitreoretinochoroidopathy (ADVIRC). (1984) (37)
- ON-pathway dysfunction and timing properties of the flicker ERG in carriers of X-linked retinitis pigmentosa. (2003) (36)
- Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases. (2002) (36)
- Improvement in visual function and fundus findings for a patient with vitamin A-deficient retinopathy. (2005) (35)
- Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations. (2002) (35)
- Abnormal axonemes in X-linked retinitis pigmentosa. (1988) (35)
- Effects of light adaptation on the response characteristics of human oscillatory potentials. (1991) (35)
- Transport of fluorescein in the ocular posterior segment in retinitis pigmentosa. (1984) (34)
- Foveal cone pigment density difference and reflectance in retinitis pigmentosa. (1986) (34)
- Rebound of macular edema with continued use of methazolamide in patients with retinitis pigmentosa. (1993) (34)
- EVALUATION OF RETINAL NERVE FIBER LAYER THICKNESS IN PATIENTS WITH RETINITIS PIGMENTOSA USING SPECTRAL-DOMAIN OPTICAL COHERENCE TOMOGRAPHY (2012) (34)
- Fundus white spots and acquired night blindness due to vitamin A deficiency (2009) (33)
- Multifocal ERG findings in carriers of X-linked retinoschisis (2006) (33)
- A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy. (2005) (32)
- Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt Disease (2016) (32)
- CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene. (2001) (32)
- Acuity-luminance and foveal increment threshold functions in retinitis pigmentosa. (1991) (32)
- Contrast response properties of magnocellular and parvocellular pathways in retinitis pigmentosa assessed by the visual evoked potential. (2004) (32)
- Laser interferometric visual acuity in senile macular degeneration. (1983) (31)
- Intersession repeatability of humphrey perimetry measurements in patients with retinitis pigmentosa. (2007) (31)
- Reproducibility of visual acuity measurements in patients with retinitis pigmentosa. (1997) (31)
- Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descent (2017) (30)
- Visual adaptation and the cone flicker electroretinogram. (1991) (30)
- Acute posterior multifocal placoid pigment epitheliopathy. (1974) (30)
- Prevalence of cystic macular lesions in patients with Usher II syndrome (2009) (29)
- Ocular histopathology of Norrie's disease. (1974) (29)
- Corneal wick electrode for recording bright flash electroretinograms and early receptor potentials. (1978) (28)
- ANTIPHOSPHOLIPID ANTIBODIES ASSOCIATED WITH RETINAL VASCULAR DISEASE (1987) (28)
- Nature of the cone ON-pathway dysfunction in melanoma-associated retinopathy. (2002) (27)
- Visual loss and foveal lesions in Usher's syndrome. (1979) (27)
- Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophy. (1997) (27)
- Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. (1994) (27)
- Drusen of the optic nerve associated with retinitis pigmentosa. (1985) (27)
- Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations. (2017) (27)
- A form of congenital stationary night blindness with apparent defect of rod phototransduction. (1990) (27)
- Prevalence of foveal lesions in type 1 and type 2 Usher's syndrome. (1995) (27)
- Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis (2000) (26)
- High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis. (2001) (26)
- Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing. (2008) (26)
- Contrast-processing deficits in melanoma-associated retinopathy. (2004) (25)
- The toxicity of intravitreal whole blood and hemoglobin (1975) (25)
- Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations. (2002) (25)
- A histopathologic study of retinitis pigmentosa (1982) (25)
- Histopathologic study of autosomal dominant vitreoretinochoroidopathy. Peripheral annular pigmentary dystrophy of the retina. (1989) (25)
- X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60. (1998) (25)
- Full-Field Pupillary Light Responses, Luminance Thresholds, and Light Discomfort Thresholds in CEP290 Leber Congenital Amaurosis Patients. (2015) (25)
- FOVEAL THICKENING IN RETINITIS PIGMENTOSA PATIENTS WITH CYSTOID MACULAR EDEMA (1994) (25)
- Electroretinographic findings in sickle cell retinopathy. (1987) (24)
- Spinal fluid pleocytosis in acute posterior multifocal placoid pigment epitheliopathy. (1977) (24)
- Electroretinographic findings in human oculocutaneous albinism. (1989) (24)
- Contrast discrimination deficits in retinitis pigmentosa are greater for stimuli that favor the magnocellular pathway (2001) (24)
- Efficacy of topical dorzolamide for treatment of cystic macular lesions in a patient with enhanced S-cone syndrome (2010) (24)
- Acquired color defects in patients with open-angle glaucoma and ocular hypertension. (1974) (24)
- Comparison of visual acuity loss in patients with different stages of Stargardt's disease. (2006) (24)
- Rod-cone dystrophy associated with a rod system electroretinogram obtained under photopic conditions. (1989) (24)
- Macular vitelliform lesion in desferrioxamine-related retinopathy (2010) (24)
- FREQUENCY OF PHOTOGRAPHICALLY APPARENT OPTIC DISC AND PARAPAPILLARY NERVE FIBER LAYER DRUSEN IN USHER SYNDROME (1996) (23)
- USHER'S SYNDROME: CNS Defects Determined by Computed Tomography (1983) (23)
- Sensitivity losses in a long wavelength sensitive mechanism of patients with retinitis pigmentosa (1982) (23)
- RETINAL THICKNESS AND VISUAL THRESHOLDS MEASURED IN PATIENTS WITH RETINITIS PIGMENTOSA (2007) (23)
- When your eyes have a wet nose: the evolution of the use of guide dogs and establishing the seeing eye. (2003) (23)
- Intraocular light scatter in patients with choroideremia. (1998) (23)
- Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations* (2013) (23)
- PSYCHOPHYSICAL MEASUREMENT OF ROD AND CONE THRESHOLDS IN STARGARDT DISEASE WITH FULL-FIELD STIMULI (2013) (22)
- Visual improvements with red-tinted glasses in a patient with cone dystrophy. (1982) (22)
- Mechanisms of rod-cone interaction: Evidence from congenital stationary nightblindness (1988) (22)
- RETROSPECTIVE LONGITUDINAL STUDY OF VISUAL ACUITY CHANGE IN PATIENTS WITH RETINITIS PIGMENTOSA (2001) (22)
- Color vision defects in retinitis pigmentosa. (1981) (21)
- Immunosuppression for autoimmune retinopathy. (2009) (21)
- Grating, vernier, and letter acuity in retinitis pigmentosa. (1992) (21)
- Macular pigment and reduced foveal short-wavelength sensitivity in retinitis pigmentosa (1987) (21)
- Synthetic activities of cultured retinal pigment epithelial cells from a patient with retinitis pigmentosa. (1985) (21)
- Light adaptation and the luminance-response function of the cone electroretinogram (2004) (21)
- Peripapillary retinal nerve fiber layer thinning in patients with autosomal recessive cone-rod dystrophy. (2009) (20)
- Microperimetry and OCT findings in female carriers of choroideremia (2010) (20)
- Dominantly inherited cystoid macular edema. A histopathologic study. (1992) (20)
- Analysis of the ABCA 4 Gene by Next-Generation Sequencing (2011) (20)
- Acquired unilateral night blindness associated with a negative electroretinogram waveform. (1996) (20)
- ASSOCIATION OF DARK-ADAPTED VISUAL FUNCTION WITH RETINAL STRUCTURAL CHANGES IN PATIENTS WITH STARGARDT DISEASE (2014) (20)
- Objective Analysis of Hyperreflective Outer Retinal Bands Imaged by Optical Coherence Tomography in Patients With Stargardt Disease. (2015) (20)
- Polymorphisms and rare sequence variants at the ROM1 locus. (1993) (19)
- Vitelliform lesions associated with retinal pigment epithelial detachment. (1978) (19)
- Dominantly inherited cystoid macular edema. (1979) (19)
- Comparative electroretinograms in argon laser and xenon arc panretinal photocoagulation. (1983) (19)
- Retinal pathology of a patient with Goldmann-Favre Syndrome (2009) (19)
- Rod influence on cone flicker detection: variation with retinal eccentricity (1986) (19)
- Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull’s Eye Maculopathy (2015) (19)
- Dark-adapted foveal thresholds and visual acuity in retinitis pigmentosa. (1986) (18)
- A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa. (2004) (18)
- Rod and cone contributions to the dark-adapted 15-Hz flicker electroretinogram (2015) (18)
- At last. A standard electroretinography protocol. (1989) (17)
- Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia (2020) (17)
- Reticular tapeto-retinal dystrophy. As a possible late stage of Sjögren's reticular dystrophy. (1976) (17)
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- Paired-flash electroretinography: a new tool to examine rod function in patients with Stargardt disease (2002) (0)
- Variability Of Full-field Erg In A Population Without Diffuse Photoreceptor Cell Disease (2002) (0)
- Mosaic Retinal Dysfunction in Obligate Carriers of Choroideremia (2006) (0)
- Cone-rod dystrophy in the Guinea baboon. (1976) (0)
- Interocular symmetry of foveal cone topography in achromatopsia (ACHM) (2018) (0)
- Retinal Histopathology in Eyes from Patients with Best Disease Caused by VMD2 Mutations (2014) (0)
- Clinical Applications of Visual Psychophysics (1982) (0)
- A BSTRACT PURPOSE : To determine outcome measures for a clinical trial of Leber congenital amaurosis ( LCA ) associated with mutations in the GUCY 2 D gene (2017) (0)
- Functional and Structural Correlations in Stargardt Macular Dystrophy (2010) (0)
- Clinical Phenotypes and Vitamin A Treatment for Sorsby’s Fundus Dystrophy (2006) (0)
- Relationship Between the High–Frequency Flicker ERG and the Derived Parameters of Cone Phototransduction in Retinitis Pigmentosa (2005) (0)
- A Molecular Screening Test for Usher Syndrome (2009) (0)
- [The importance of viruses in the development of acute angina]. (1969) (0)
- Contrast polarity and letter identification (1992) (0)
- Clinical Features of a Severe Form of Autosomal Dominant Retinitis Pigmentosa in a Large Family with a Novel IMPDH1 Mutation (ARG231PRO) (2003) (0)
- Current Ocular Therapy (1995) (0)
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