Gerald Allen Fishman

Gerald Allen Fishman's AcademicInfluence.com Rankings

Biology

#6537

World Rank

#9274

Historical Rank

Molecular Biology

#683

World Rank

#700

Historical Rank

Biochemistry

#845

World Rank

#952

Historical Rank

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Biology

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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)
Novel de novo mutation in a patient with Best macular dystrophy. (2006) (17)
Gene dosage manipulation alleviates manifestations of hereditary PAX6 haploinsufficiency in mice (2020) (17)
Electrophysiology and inherited retinal disorders (1985) (17)
Spectral transmission characteristics of tinted lenses. (1981) (17)
Peripheral vision screening for driving in retinitis pigmentosa patients. (1991) (17)
Comparison of intraocular light scatter in carriers of choroideremia and X-linked retinitis pigmentosa. (2002) (17)
Interocular amplitude differences of the full field electroretinogram in normal subjects (2003) (17)
USE OF A CARBONIC ANHYDRASE INHIBITOR IN X-LINKED RETINOSCHISIS: Effect on Cystic-Appearing Macular Lesions and Visual Acuity (2017) (17)
Activation phase of cone phototransduction and the flicker electroretinogram in retinitis pigmentosa (2006) (17)
INFRARED SCANNING LASER OPHTHALMOSCOPE IMAGING OF THE MACULA AND ITS CORRELATION WITH FUNCTIONAL LOSS AND STRUCTURAL CHANGES IN PATIENTS WITH STARGARDT DISEASE (2011) (17)
Letter contrast sensitivity in retinitis pigmentosa patients assessed by Regan charts. (1989) (17)
Lymphocyte subpopulations and S-antigen reactivity in retinitis pigmentosa. (1985) (16)
Vitreous fluorophotometry in patients with fundus flavimaculatus. (1982) (16)
The application of chromatic dark-adapted kinetic perimetry to retinal diseases. (2003) (16)
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation. (2004) (16)
Diagnosis in a patient with fundus albipunctatus and atypical fundus changes (2009) (16)
Characteristics of contrast processing deficits in X-linked retinoschisis (2005) (16)
Historical evolution in the understanding of Stargardt macular dystrophy (2010) (16)
Dark adaptation testing in heterozygotes of Usher's syndrome. (1979) (16)
Spectral transmission characteristics of intraocular and aphakic contact lenses. (1983) (16)
STRUCTURAL AND FUNCTIONAL CHARACTERISTICS IN CARRIERS OF X-LINKED RETINITIS PIGMENTOSA WITH A TAPETAL-LIKE REFLEX (2010) (16)
PERIPHERAL VISUAL FIELD LOSS AND DRIVING PERFORMANCE (1991) (15)
MAGNETIC RESONANCE IMAGING OF CENTRAL NERVOUS SYSTEM DEFECTS IN USHER'S SYNDROME (1987) (15)
Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations (2016) (15)
X-Linked Retinitis Pigmentosa: Current Status (2001) (15)
Retinal Dysfunction in Carriers of Bardet-Biedl Syndrome (2007) (15)
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease. (2021) (14)
Correlation of electroretinographic findings and peripheral retinal nonperfusion in patients with sickle cell retinopathy. (1990) (14)
Discrimination of spatial displacements by patients with retinitis pigmentosa (1998) (14)
THE VALUE OF RETINAL IMAGING WITH INFRARED SCANNING LASER OPHTHALMOSCOPY IN PATIENTS WITH STARGARDT DISEASE (2014) (14)
Deficits in temporal integration for contrast processing in retinitis pigmentosa. (2003) (14)
A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa. (1998) (14)
Loss of color vision and Stiles' II1 mechanism in a patient with cerebral infarction. (1980) (14)
Cellular immune function of patients with retinitis pigmentosa. (1986) (14)
Flecked-Retina Syndromes (2009) (13)
Identification of Novel Mutations in Patients With Leber Congenital Amaurosis by Genome-Wide Homozygosity Mapping With SNP Microarrays (2007) (13)
The electro-oculogram in diffuse (familial) drusen. (1976) (12)
Refractive errors in patients with fundus flavimaculatus. (1982) (12)
Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with stargardt disease (2010) (12)
Abnormal Distribution of Red/Green Cone Opsins in a Patient with an Autosomal Dominant Cone Dystrophy (2005) (12)
Granulomatous anterior uveitis presenting with acute posterior multifocal placoid pigment epitheliopathy (2005) (12)
Early receptor potential measurements in human ocular siderosis. (1983) (12)
Electro-oculogram testing in fundus flavimaculatus. (1979) (12)
Disease Expression of RP 1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa (2000) (12)
Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities. (2001) (11)
Phenotypic expression of a PRPF8 gene mutation in a Large African American family. (2008) (11)
Effects of chondroitin sulfate on cultured human retinal pigment epithelial cells. (1991) (11)
Effect of Methazolamide on Chronic Macular Edema in Patients with Retinitis Pigmentosa (1995) (11)
Equivalent intrinsic noise, sampling efficiency, and contrast sensitivity in patients with retinitis pigmentosa. (2013) (11)
VISUAL ACUITY IN PATIENTS WITH STARGARDT DISEASE AFTER AGE 40 (2017) (11)
Abnormal foveal spectral sensitivity in retinitis pigmentosa. (1987) (11)
Blood-retinal barrier function in patients with cone or cone-rod dystrophy. (1986) (11)
Structural and Functional Measures of Inner Retinal Integrity Following Visual Acuity Improvement in a Patient with Hereditary Motor and Sensory Neuropathy Type VI (2011) (11)
Stop mutations in exon 6 of the choroideremia gene, CHM, associated with preservation of the electroretinogram. (2005) (11)
Resolution of Mid-Peripheral Schisis in X-Linked Retinoschisis with the Use of Dorzolamide (2014) (11)
Stereoacuity testing in patients with retinal and optic nerve disorders (1995) (11)
VISUAL IMPAIRMENT IN RETINITIS PIGMENTOSA. (2019) (11)
Temporal properties of letter identification in retinitis pigmentosa. (1993) (11)
ELECTRORETINOGRAPHY AND INHERITED MACULAR DYSTROPHIES (1985) (11)
Five novel RPGR mutations in families with X‐linked retinitis pigmentosa (2001) (11)
Research update: report on retinitis pigmentosa and the immune system workshop 7-8 November 1985. (1986) (10)
Electrophysiological Assessment of Cone ON-Pathway Dysfunction in Melanoma-Associated Retinopathy (2002) (10)
CLINICAL CHARACTERIZATION OF STARGARDT DISEASE PATIENTS WITH THE p.N1868I ABCA4 MUTATION. (2019) (10)
Allelic Variation in the VMD 2 Gene in Best Disease and Age-Related Macular Degeneration (2000) (10)
Traumatically acquired color vision defect. (1980) (10)
Progressive human cone-rod dysfunction (dystrophy). (1976) (10)
SHORT-TERM INTERVISIT VARIABILITY OF ERG AMPLITUDES IN NORMAL SUBJECTS AND PATIENTS WITH RETINITIS PIGMENTOSA (2005) (9)
Atlas of Indocyanine Green Angiography (1996) (9)
Nondetectable electroretinogram in combined methylmalonic aciduria and homocystinuria. (1992) (9)
Higher-Order Wavefront Aberrations in Retinitis Pigmentosa (2005) (9)
Retinal Nerve Fiber Thickness Measurements In Choroideremia Patients With Spectral-Domain Optical Coherence Tomography (2011) (9)
Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy (2019) (9)
GYRATE ATROPHY‐LIKE PHENOTYPE WITH NORMAL PLASMA ORNITHINE (1997) (9)
The loss of night vision: clinical manifestations in man and animals (1990) (9)
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations. (1999) (9)
Two-color pupillometry in KCNV2 retinopathy (2019) (8)
EFFECT OF VITAMIN A TREATMENT ON THE PROLONGATION OF DARK ADAPTATION IN STARGARDT'S DYSTROPHY (1994) (8)
Rhodopsin F45L Allele Does Not Cause Autosomal Dominant Retinitis Pigmentosa in a Large Caucasian Family. (2013) (8)
Retinal and pigment epithelial alterations over choroidal malignant melanomas. (1975) (8)
The Prevalence of Macular Cysts in Patients with Clinical Cone-Rod Dystrophy Determined by Spectral-Domain Optical Coherence Tomography (2014) (8)
Night blindness secondary to vitamin A deficiency in a patient with bile duct strictures after liver transplantation. (1998) (8)
Dark adaptation in patients with Best vitelliform macular dystrophy. (1994) (8)
Spontaneous improvement of rod system function in a patient with melanoma-associated retinopathy. (2008) (8)
Rod-cone interaction in flicker perimetry: evidence for a distal retinal locus (1985) (8)
The Susceptible Visual Apparatus (1992) (8)
Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal disease. (1998) (8)
Dorzolamide use in the management of macular cysts in a patient with enhanced s-cone syndrome. (2009) (7)
Ceroid-lipofuscinosis (Batten's Disease) (1984) (7)
Full-Field Electroretinography, Pupillometry, and Luminance Thresholds in X-Linked Retinoschisis (2020) (7)
LEGAL BLINDNESS AND EMPLOYMENT IN PATIENTS WITH JUVENILE‐ONSET MACULAR DYSTROPHIES OR ACHROMATOPSIA (1998) (7)
Carriers of X-linked recessive retinitis pigmentosa: investigation by vitreous fluorophotometry (1981) (7)
Birdshot retinochoroidopathy. (1984) (7)
Vitreous fluorophotometry in carriers of choroideremia and X-linked retinitis pigmentosa. (1989) (7)
Color vision in albino subjects (1983) (7)
Prolonged rod dark adaptation in patients with cone-rod dystrophy. (1994) (7)
Rubella maculopathy. (1980) (6)
Electroretinographic Findings in a Patient with Congenital Stationary Night Blindness Due to a Novel NYX Mutation (2013) (6)
CRB 1 Gene Mutations Are Associated with Keratoconus in Patients with Leber Congenital Amaurosis (2009) (6)
John Dalton: Though in Error, He Still Influenced Our Understanding of Congenital Color Deficiency (2008) (6)
BASIC PRINCIPLES OF CLINICAL ELECTRORETINOGRAPHY (1985) (6)
A Method for Differentiating Ocular Higher-Order Aberrations From Light Scatter Applied to Retinitis Pigmentosa (2005) (6)
Coherence and the judgment of spatial displacements in retinitis pigmentosa (1999) (6)
Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations (2021) (5)
STRUCTURAL AND FUNCTIONAL MONITORING OF EXTRAMACULAR CYSTOID SPACES IN A CASE OF X-LINKED RETINOSCHISIS TREATED WITH ACETAZOLAMIDE (2016) (5)
Prevalence of Mutations in the RPE65, CRX, AIPL1, TULP1, GUCY2D and CRB1 Genes in Leber Congenital Amaurosis (2003) (5)
Two Additional Benefits of Dark Glasses on Rod Vision in Patients with Congenital Achromatopsia (1983) (5)
Rod increment thresholds in cone-rod dystrophy. (1989) (5)
Psychological Profiles of Patients with Central Vision Loss (2000) (4)
Attainment of educational levels in patients with Leber's congenital amaurosis. (2006) (4)
Source Book of Ophthalmology (1996) (4)
VISUAL ACUITY LOSS IN RECESSIVE RETINITIS PIGMENTOSA AND ITS CORRELATION WITH MACULAR LESIONS (2011) (4)
Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis (2016) (4)
Interferon-gamma production and HLA-DR expression in patients with retinitis pigmentosa. (1987) (4)
De novo mutation in a choroideremia carrier. (2007) (4)
Leber Congenital Amaurosis gene therapy clinical trial (2009) (3)
Presurgical Evaluation of Eyes with Opaque Media (1983) (3)
Manual of Retinal and Choroidal Dystrophies (1982) (3)
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia (2021) (3)
Cellular Changes in Retinas From Patients With BEST1 Mutations (2020) (2)
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure (2021) (2)
Contrast Sensitivity and Equivalent Intrinsic Noise in X-Linked Retinoschisis (2022) (2)
ON-response deficits in X-Linked juvenile retinoschisis assessed by Sawtooth Flicker electroretinogram (2000) (2)
A historical perspective on the early treatment of night blindness and the use of dubious and unproven treatment strategies for patients with retinitis pigmentosa. (2013) (2)
Relationship Between Performance of Tasks of Daily Living and Tests of Visual Function in Patients with Retinitis Pigmentosa (1998) (2)
Challenges associated with clinical trials for inherited and orphan retinal diseases. (2005) (2)
Chapter 43 – Hereditary Choroidal Diseases (2013) (2)
Luminance Thresholds and Their Correlation With Retinal Structure in X-Linked Retinoschisis (2021) (2)
Efficacy of brinzolamide ophthalmic suspension 1% for treatment of a vitelliform macular lesion in a patient with desferrioxamine retinopathy. (2011) (2)
Effect of mydriasis on visual field area in retinitis pigmentosa. (1992) (2)
Visual Electrodiagnostic Testing: A Practical Guide for the Clinician (1982) (2)
Transplantation of retinal pigment epithelial cells. Scientific advance and social responsibility. (1988) (2)
Educational levels in patients with stargardt disease. (2010) (2)
Prolonged roddarkadaptation inretinitis pigmentosa (1984) (2)
Is There an Association of Anti–Retinal Antibodies and Cystoid Macular Edema in Patients With Retinitis Pigmentosa? (2006) (2)
Dealing with Genes: The Language of Heredity. Paul Berg and Maxine Singer. Mill Valley, University Science Books, 1992 (1993) (2)
Sinclair swine with spontaneously regressing cutaneous melanomas do not have autoantibodies against retinal bipolar cells. (1996) (2)
Photoreceptor Analysis in the Retina of a Donor With Goldmann-Favre Syndrome (2008) (1)
The Prevalence of Cystoid Macular Edema on Optical Coherence Tomography in Retinitis Pigmentosa Patients Without Evidence of Cystic Changes on Fundus Exam (2008) (1)
Calibration error in dark adaptometer. (1978) (1)
Residual Cone Structure in Achromatopsia: Implications for Gene Therapy (2014) (1)
Longitudinal Imaging of Foveal Cone Structure in Congenital Achromatopsia (2015) (1)
The Vitreous: Structure, Function, and Pathobiology (1990) (1)
Degenerative Retinopathies: Advances in Clinical and Genetic Research (1994) (1)
Presence and Treatment of Cystoid Macular Edema in Patients with Choroideremia (2011) (1)
Driving performance ofretinitis pigmentosa patients (1981) (1)
Vision Improvement After Retreatment with an Oral Synthetic cis-Retinoid (QLT091001) in Subjects with LCA or RP due to Mutations in RPE65 or LRAT (2015) (1)
Best dystrophy in a patient with an ocular histoplasmosis phenotype. (2004) (1)
High-resolution Imaging of Photoreceptor Structure in Choroideremia (2012) (1)
Interocular difference and duration for doubling of the minimal angle of visual resolution in patients with Stargardt disease. (2009) (1)
Exon screening of the genes encoding the β- and γ-subunits of cone transducin in patients with inherited retinal disease (1998) (1)
Inherited Retinal Diseases: A Diagnostic Guide (1990) (1)
Assessing Photoreceptor Reflectance And Structure In Congenital Stationary Night Blindness (2012) (1)
Vitreochorioretinal degeneration associated with trichomegaly. (1976) (1)
Recessive RPGRIP1 mutations can cause rod and cone dysfunction in the heterozygous parents. (2004) (1)
Equipment for the Measurement of Visual Evoked Cortical Potentials (1984) (1)
Electrophysiological and Pupillometric Abnormalities in PROM1 Cone–Rod Dystrophy (2020) (1)
Evaluation of Pure Tone and Speech Discrimination Changes in Usher's Syndrome (1989) (1)
The Phenotypes of Patients and Heterozygous Carriers With RDH12 Mutations Are Different From Those With RPE65 Mutations (2005) (1)
Racial differences in the prevalence of atrophic-appearing macular lesions between black and white patients with retinitis pigmentosa. (1994) (1)
Retrospective analysis of 58 children with retinoblastoma. (1984) (1)
Disease-Causing Mutations in the RPE65 Gene Abolish Retinoid Isomerase Activity (2007) (1)
Evaluation of Retinal Nerve Fiber Layer Thickness in Retinitis Pigmentosa Patients Using Spectral-Domain OCT (2012) (1)
Retinal Structure and Function in a Pedigree Cosegregating Achromatopsia and a Rhodopsin Mutation (2012) (1)
Controversies of Diagnosing Autoimmune Retinopathy--Reply (2010) (1)
Perifoveal Inner Retinal Thinning as an Early Sign of Hydroxychloroquine Retinal Toxicity (2010) (1)
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease (2022) (1)
Pathognomonic macular ripples are revealed by polarized infrared retinal imaging (2021) (1)
Optical Quality of the Eye in Retinitis Pigmentosa. (2004) (1)
Harmonic Analysis of the Strobe Flicker Electroretinogram in Retinal Disease (1997) (0)
Diagnostic and therapeutic challenges. (2011) (0)
Cone ON-pathway defect contributes to ERG implicit time delays in carriers of X-linked retinitis pigmentosa (XLRP) (2002) (0)
Pupillary Responses To Offset And Onset Of Isolated Rod And Cone Stimuli Using A 4-Primary Photostimulating Method (2012) (0)
Glare and Contrast Sensivity for Clinicians (1991) (0)
Retina Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP 290 Gene (2017) (0)
Structural and functional monitoring of extramacular cystoid spaces in X-linked retinoschisis treated with carbonic anhydrase inhibitors (2015) (0)
The Value of Retinal Imaging and Functional Testing of Patients with Stargardt Disease (2013) (0)
Release of Scientific Information to the News Media-Reply (1989) (0)
A Method for Measurements of Higher Order Aberrations and Light Scatter in Human Eyes (2005) (0)
Retinal and Choroidal Manifestations of Systemic Disease (1992) (0)
DELAYED ON RESPONSE OF THE CONE SYSTEM IN NIGHT BLINDNESS (1999) (0)
Acuity-luminance functions in retinitis pigmentosa (1988) (0)
A Strategy for Efficient Molecular Diagnosis of Genetically Heterogeneous Autosomal Recessive Diseases (2007) (0)
Differences in Spectral-Domain Optical Coherence Tomography (SD-OCT) and Fundus Autofluorescence Characteristics of Fundus Lesions in Patients With Fundus Albipunctatus and Retinitis Punctata Albescens (2010) (0)
Simplex Crumbs Homologue 1 Maculopathy Masquerading as Juvenile X-Linked Retinoschisis in Male Patients (2020) (0)
Rod–cone interactions in congenital stationary night blindness (1986) (0)
Full-field measures of visual function in X-linked retinoschisis: comparison of ERGs, luminance thresholds, and pupil responses (2017) (0)
[Indices of Staphylococcus and Streptococcus antibodies in the blood of patients with multiform exudative erythema]. (1975) (0)
Hydroxychloroquine Alters the ERG in an Animal Model of ADRP (the Pigmented P23H Rat) (2005) (0)
Objective analysis of outer retinal layers imaged by optical coherence tomography in patients with Stargardt disease. (2015) (0)
Unanticipated prognosis for a patient with type 2 Usher syndrome (2019) (0)
Letter to the EditorAuthor reply (2009) (0)
Natural Course of Visual Field Loss in Patients With Usher Syndrome Type 2 (2006) (0)
Mutations In Lca9 Cause Human Congenital Blindness Due To Leber Congenital Amaurosis (2012) (0)
Assessment of Macular Pigment in Retinitis Pigmentosa Using Digitized Television Fundus Reflectometry (1986) (0)
Melanoma-Associated Retinopathy (MAR) Immunoglobins Target Both Rod and Cone ON Bipolar Cells (2009) (0)
Visual acuity in Stargardt disease patients after age 40 (2017) (0)
Frequent hypomorphic alleles solve 80% of late-onset ABCA4 disease and distinguish it from age-related macular degeneration (2017) (0)
(OD-175)MELANOMA-ASSOCIATED AND CANCER-ASSOCIATED RETINOPATHY: TWO VISUAL PARANEOPLASTIC SYNDROMES: Poster # 69 (2000) (0)
North Carolina macular dystrophy: mutations found in 12 additional families (2017) (0)
Visual Acuity Loss in 270 Patients with Stargardt Disease (2002) (0)
Genetic Analyses of Autosomal Recessive Choroideremia-Like Pedigrees (2010) (0)
Reply: To PMID 24280667. (2015) (0)
The Phenotype of Lca Patients With Mutations in Cep290 (2008) (0)
Retina Residual Foveal Cone Structure in CNGB 3-Associated Achromatopsia (2016) (0)
Rod Sensitivity Loss in Patients with Stargardt Disease and its Correlation with Retinal Structural Changes (2012) (0)
Visual loss andfoveal lesions inUsher's syndrome (1979) (0)
Human Macular Pigment Measured by Imaging Fundus Reflectometry (1987) (0)
Spontaneous Improvement in Rod System Function in Melanoma-Associated Retinopathy (2007) (0)
Pathology Of The Eye Of A 30 Year Old Male With Choroideremia (2006) (0)
Cone Isolating Electroretinograms In Individuals With A Mutant Opsin Allele Associated With Cone Dystrophy (2012) (0)
inargonlaser andxenon arcpanretinal photocoagulation (1983) (0)
Brit . Y . Ophthal . ( 1976 ) 6 o , 345 Diagnostic features of the Favre-Goldmann syndrome (2004) (0)
Paired-flash electroretinography (2002) (0)
Electroretinography in sickle cell retinopathy (1987) (0)
VITREOUS FLUOROPHOTOMETRY IN PATIENTS WITH BEST'S MACULAR DYSTROPHY (1990) (0)
Macular Degeneration-Reply (1984) (0)
Electrodiagnostic Testing of the Visual System: A Clinical Guide (1993) (0)
"Saturation" of the Dark-Adapted b-Wave (1988) (0)
DGGE and SSCPE screening of the gene for the gamma subunit of cone transducin in patients with cone disease (1996) (0)
Favre-Goldmann syndrome . Diagnostic features of the (2004) (0)
Macular Degeneration; Retinal Detachment and Vitreous Surgery; Diagnosis and Management of Diabetic Retinopathy (1990) (0)
A Method for Deducing the Pathogenic Contribution of Individual Recessive Disease Alleles (2009) (0)
Spatial and Temporal Integration Abnormalities in X-Linked Retinoschisis (2022) (0)
Alex E. Krill: A brief biography of his life and final days (2005) (0)
Cystic Macular Lesions in Patients With Retinitis Pigmentosa—Reply (2011) (0)
Indocyanine green toxicity of the retina after cataract surgery: a case report. (2009) (0)
Variations in NPHP5 Cause Nonsyndromic Leber Congenital Amaurosis (LCA) (2010) (0)
Supernormal Scotopic ERG in Macular Dystrophy (1983) (0)
Changes in the Derived Parameters of Cone Phototransduction During Light Adaptation (2005) (0)
Prevalence of Cystic Macular Lesions in Patients with Type II Usher Syndrome (2008) (0)
Rod and cone responses in the flicker ERG (1985) (0)
Diagnostic and Therapeutic Challenges Section of Retina (2009) (0)
Topical Dorzolamide for the Treatment of Macular Edema in Patients With Retinitis Pigmentosa (2005) (0)
Determination of spatially resolved visual pigment density by a television ophthalmoscope image processor (1980) (0)
Mutations in the GRM6 Gene Encoding the Mglur6 Receptor in Patients With Autosomal Recessive Night Blindness and Abnormal Cone ERG on Responses (2005) (0)
Novel Expression of RPGRIP1 and Functional Analysis of Heterozygous Nonsense Mutations (2005) (0)
Assessment of Foveal Function in Retinitis Pigmentosa (1985) (0)
Five Novel RPGR Mutation in brief: Mutations in Families with XLinked Retinitis Pigmentosa (2000) (0)
Assessing color vision in congenital achromatopsia (2016) (0)
Clinical Decisions in Medical Retinal Disease (1996) (0)
Whole-exome sequencing in patients with STGD (ABCA4)-like phenotypes (2015) (0)
Early Detection of Functional Changes Using Microperimetry on Patients with Subclinical Hydroxychloroquine Toxicity (2012) (0)
Postmortem Analysis Of Cone Opsins In A Patient With An Autosomal Dominant Cone Dystrophy. (2004) (0)
[Some immunologic indices in allergic rhinitis of bacterial nature associated with chronic tonsillitis]. (1971) (0)
Men of Vision (1995) (0)
culty in performing everyday activities in patients with juvenile macular dystrophies : comparison with patients with retinitis pigmentosa (1998) (0)
A Variant in the 5'UTR of the Cone Gene Encoding the Cone Gamma Subunit of cGMP-PDE that Causes Overexpression of the Protein; Disease-causing Mutation or Rare Polymorphism? (2003) (0)
Assessing Cone Structure in Achromatopsia With AOSLO and SDOCT (2016) (0)
Stimulus Duration and Visual Acuity in Retinitis Pigmentosa (1991) (0)
Parallel Processing in the Visual Systems: The Classification of Retinal Ganglion Cells and Impact on the Neurobiology of Vision (1984) (0)
Imaging Photoreceptor Structure in Achromatopsia Patients Using Adaptive Optics and Spectral -Domain Optical Coherence Tomography (2011) (0)
Association Between Retinal Thickness and Visual Thresholds in Patients With Retinitis Pigmentosa (2006) (0)
Intrasession and Intersession Repeatability of Retinal Sensitivity Using a Modified Nidek MP-1 Microperimeter in Patients with Stargardt Disease (2012) (0)
Analysis of ABCA4 mutation spectrum in Stargardt/ABCA4 disease (2019) (0)
Abnormal rod- and cone-isolated flicker electroretinograms in carriers of X-linked retinoschisis (2015) (0)
Atlas of Intraocular Tumors (1994) (0)
Analysis of small recessive RP families for mutations in candidate genes (1996) (0)
Relationship Between Visual Acuity and Contrast Sensitivity Deficits in Retinitis Pigmentosa (1993) (0)
The Man Behind the Syndrome (1990) (0)
[Etiological role of nonspecific microflora in bronchopulmonary pathology (based on bacteriological and immunological data)]. (1975) (0)
Adaptation-dependent response properties of the cone system flicker electroretinogram (1990) (0)
We wish to thank all of the reviewers who have generously and thoughtfully assisted the Editorial Board, our authors, and our readers during the past year. Their efforts have helped us get timely decisions to authors. (2015) (0)
Full-field luminance thresholds, light discomfort thresholds, and pupillary light responses in CEP290 Leber congenital amaurosis patients. (2014) (0)
Refractive errorsofretinitis pigmentosa patients (2012) (0)
Compound Heterozygous Inheritance of Best Vitelliform Macular Dystrophy (2008) (0)
ABCA4 Sequence Variations in Patients with Cone-Rod Dystrophy (2002) (0)
AOn ' Response Defect in Paraneoplastic Night Blindness With Cutaneous Malignant Melanoma (2005) (0)
Di Y culty in performing everyday activities in patients with juvenile macular dystrophies: comparison with patients with retinitis pigmentosa (1998) (0)
Visual Acuity Loss and Its Correlation to Macular Lesions in Recessive Retinitis Pigmentosa (2010) (0)
Novel CRALBP Mutations Associated With Retinitis Punctata Albescens: Further Evidence Of Genetic Heterogeneity (2002) (0)
Spatial frequency characteristics of contrast processing deficits in retinitis pigmentosa (2010) (0)
Leber Congenital Amaurosis (LCA) Patients With Possible Mutations in Two Ciliary Genes: CEP290 and RPGRIP1. Does Oligogenic Inheritance Exist in LCA? (2008) (0)
Peripapillary Retinal Nerve Fiber Layer Thickness in RP Patients (2007) (0)
Jan Evangelista Purkinje: Visual Physiologist (2017) (0)
Heterozygous Carriers (Parents of Offspring With Leber Congenital Amaurosis) With CRB1 Mutations Have a Focal Retinal Dysfunction (2005) (0)
The effect of spatial sampling on the visibility of letters and gratings (1993) (0)
Novel frameshift mutations in CRX associated with de novo and autosomal dominant Leber Congenital Amaurosis (2021) (0)
Fundus Changes in Heterozygote Carriers in a Family with Novel Mutations in the RLBP1 (CRALBP) Gene (2002) (0)
[Dynamics of immunological indices under the effect of specific desensitization therapy in patients with recurrent aphthous stomatitis]. (1974) (0)
Clinical Phenotypes Associated with Specific Genotypes in Leber Congenital Amaurosis (LCA). (2004) (0)
CERKL Mutations Cause Retina-Wide Cone and Rod Disease With Prominent Maculopathy (2009) (0)
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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