David G. Birch
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Engineering Computer Science
David G. Birch's Degrees
- PhD Computer Science Stanford University
- Masters Electrical Engineering University of California, Berkeley
- Bachelors Computer Engineering University of California, Berkeley
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(Suggest an Edit or Addition)David G. Birch's Published Works
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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
- Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice (1999) (842)
- Effect of Dietary Omega-3 Fatty Acids on Retinal Function of Very-Low-Birth-Weight Neonates (1990) (557)
- Visual Acuity and the Essentiality of Docosahexaenoic Acid and Arachidonic Acid in the Diet of Term Infants (1998) (507)
- Dietary essential fatty acid supply and visual acuity development. (1992) (457)
- Essential fatty acids in visual and brain development (2001) (438)
- A randomized controlled trial of early dietary supply of long‐chain polyunsaturated fatty acids and mental development in term infants (2000) (413)
- Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids. (1992) (344)
- Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness (2000) (332)
- Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies (2001) (298)
- A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants. (2000) (286)
- A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. (1998) (280)
- Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis (2000) (279)
- Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical Trial. (2016) (272)
- Standardized full-field electroretinography. Normal values and their variation with age. (1992) (269)
- Ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for treatment of geographic atrophy in age-related macular degeneration (2011) (267)
- Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families. (2006) (263)
- Natural course of retinitis pigmentosa over a three-year interval. (1985) (248)
- Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice. (2008) (237)
- Breast-feeding and optimal visual development. (1993) (232)
- Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave. (1994) (229)
- A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. (2002) (229)
- Long-Term Results from an Epiretinal Prosthesis to Restore Sight to the Blind. (2015) (227)
- Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degeneration. (2001) (226)
- Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa. (2002) (209)
- Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements (2014) (205)
- Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography. (2009) (195)
- The Very Large G-Protein-Coupled Receptor VLGR1: A Component of the Ankle Link Complex Required for the Normal Development of Auditory Hair Bundles (2006) (195)
- Disruption of a Retinal Guanylyl Cyclase Gene Leads to Cone-Specific Dystrophy and Paradoxical Rod Behavior (1999) (193)
- A quantitative measure of the electrical activity of human rod photoreceptors using electroretinography (1990) (186)
- Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration. (2005) (186)
- Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial (2016) (183)
- Visual and brain function measurements in studies of n-3 fatty acid requirements of infants. (1992) (175)
- A computational model of the amplitude and implicit time of the b-wave of the human ERG (1992) (174)
- The A-wave of the human electroretinogram and rod receptor function. (1990) (173)
- Visual maturation of term infants fed long-chain polyunsaturated fatty acid-supplemented or control formula for 12 mo. (2005) (173)
- A randomized controlled trial of long-chain polyunsaturated fatty acid supplementation of formula in term infants after weaning at 6 wk of age. (2002) (171)
- Prevalence of AIPL1 mutations in inherited retinal degenerative disease. (2000) (169)
- Visual function in breast-fed term infants weaned to formula with or without long-chain polyunsaturates at 4 to 6 months: a randomized clinical trial. (2003) (166)
- Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis (2000) (166)
- Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa. (2013) (165)
- Normative reference ranges for the retinal nerve fiber layer, macula, and retinal layer thicknesses in children. (2013) (160)
- Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy. (1999) (159)
- Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis. (2006) (157)
- Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing (2013) (143)
- Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa. (2013) (143)
- Beta wave of the scotopic (rod) electroretinogram as a measure of the activity of human on-bipolar cells. (1996) (138)
- Impact of Early Dietary Intake and Blood Lipid Composition of Long-Chain Polyunsaturated Fatty Acids on Later Visual Development (2000) (138)
- Human cone receptor activity: The leading edge of the a–wave and models of receptor activity (1993) (137)
- Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1. (2004) (137)
- Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity (1993) (136)
- The transition zone between healthy and diseased retina in patients with retinitis pigmentosa. (2011) (135)
- Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps (2018) (134)
- GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. (2012) (126)
- The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1. (2016) (120)
- Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. (1995) (116)
- Retinitis pigmentosa. A symposium on terminology and methods of examination. (1983) (114)
- A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa. (2010) (114)
- A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa. (2004) (114)
- Safety and efficacy of omega-3 fatty acids in the nutrition of very low birth weight infants: soy oil and marine oil supplementation of formula. (1994) (114)
- Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa. (2013) (113)
- The inner segment/outer segment border seen on optical coherence tomography is less intense in patients with diminished cone function. (2011) (111)
- Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4 (2007) (110)
- Effects of supplementation with omega 3 long-chain polyunsaturated fatty acids on retinal and cortical development in premature infants. (1993) (109)
- The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations. (2004) (106)
- Electrophysiologic Testing in Disorders of the Retina, Optic Nerve and Visual Pathway (1990) (106)
- Phototransduction in human cones measured using the a-wave of the ERG (1995) (106)
- Rod ERGs in retinitis pigmentosa and cone-rod degeneration. (1987) (105)
- Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. (2012) (101)
- Role of essential fatty acids in the function of the developing nervous system (2007) (99)
- Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa. (1997) (97)
- Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors. (1997) (95)
- The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development. (2005) (94)
- Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa. (2009) (93)
- Photoresponses of human rods in vivo derived from paired-flash electroretinograms (1997) (93)
- Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. (1999) (91)
- Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing (2016) (90)
- Allelic Heterogeneity and Genetic Modifier Loci Contribute to Clinical Variation in Males with X-Linked Retinitis Pigmentosa Due to RPGR Mutations (2011) (85)
- Long-term Follow-up of Patients With Retinitis Pigmentosa Receiving Intraocular Ciliary Neurotrophic Factor Implants. (2016) (84)
- SAFETY AND EFFECT ON ROD FUNCTION OF ACU-4429, A NOVEL SMALL-MOLECULE VISUAL CYCLE MODULATOR (2012) (82)
- Identification of disease-causing mutations in autosomal dominant retinitis pigmentosa (adRP) using next-generation DNA sequencing. (2011) (82)
- Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases. (2011) (80)
- A comparison of progressive loss of the ellipsoid zone (EZ) band in autosomal dominant and x-linked retinitis pigmentosa. (2014) (80)
- Genomic rearrangements of the PRPF31 gene account for 2.5% of autosomal dominant retinitis pigmentosa. (2006) (79)
- Method for deriving visual field boundaries from OCT scans of patients with retinitis pigmentosa (2011) (79)
- Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa (2001) (78)
- Diurnal rhythm in the human rod ERG. (1984) (77)
- Age-related macular degeneration: a target for nanotechnology derived medicines (2007) (74)
- Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease, and test-retest variability. (2002) (73)
- Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP). (2011) (70)
- Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9) (2017) (67)
- Docosahexaenoic acid in red blood cells of patients with X-linked retinitis pigmentosa. (1995) (67)
- Relationships among multifocal electroretinogram amplitude, visual field sensitivity, and SD-OCT receptor layer thicknesses in patients with retinitis pigmentosa. (2012) (66)
- CLINICAL ENDPOINTS FOR THE STUDY OF GEOGRAPHIC ATROPHY SECONDARY TO AGE-RELATED MACULAR DEGENERATION (2016) (66)
- A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27. (1998) (63)
- Impaired synthesis of DHA in patients with X-linked retinitis pigmentosa. (2001) (62)
- S-cone function in patients with retinitis pigmentosa. (1993) (62)
- Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) gene. (2001) (62)
- Assessing abnormal rod photoreceptor activity with the a-wave of the electroretinogram: Applications and methods (1996) (62)
- Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration. (2008) (61)
- Abnormalities of the retinal cone system in retinitis pigmentosa (1996) (61)
- Rates of decline in regions of the visual field defined by frequency-domain optical coherence tomography in patients with RPGR-mediated X-linked retinitis pigmentosa. (2015) (60)
- Current popularity of pneumatic retinopexy. (1999) (60)
- Psychophysical assessment of low visual function in patients with retinal degenerative diseases (RDDs) with the Diagnosys full-field stimulus threshold (D-FST) (2009) (59)
- Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography. (2016) (58)
- A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa (1993) (58)
- Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7 (2017) (56)
- The relationship between rod perimetric thresholds and full-field rod ERGs in retinitis pigmentosa. (1987) (56)
- 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)
- The Stiles-Crawford effect in retinitis pigmentosa. (1982) (52)
- Four-year placebo-controlled trial of docosahexaenoic acid in X-linked retinitis pigmentosa (DHAX trial): a randomized clinical trial. (2014) (51)
- Biological safety assessment of docosahexaenoic acid supplementation in a randomized clinical trial for X-linked retinitis pigmentosa. (2003) (50)
- Measurement and Reproducibility of Preserved Ellipsoid Zone Area and Preserved Retinal Pigment Epithelium Area in Eyes With Choroideremia. (2017) (50)
- The focal electroretinogram in the clinical assessment of macular disease. (1989) (50)
- The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa. (2007) (49)
- Loss of Caveolin-1 Impairs Retinal Function Due to Disturbance of Subretinal Microenvironment* (2012) (49)
- A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa. (2014) (47)
- Recovery kinetics of human rod phototransduction inferred from the two-branched alpha-wave saturation function. (1996) (47)
- Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. (1998) (47)
- PHASE II, RANDOMIZED, PLACEBO-CONTROLLED, 90-DAY STUDY OF EMIXUSTAT HYDROCHLORIDE IN GEOGRAPHIC ATROPHY ASSOCIATED WITH DRY AGE-RELATED MACULAR DEGENERATION (2015) (46)
- Fatty acid profile of buccal cheek cell phospholipids as an index for dietary intake of docosahexaenoic acid in preterm infants (1999) (45)
- Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11. (2019) (45)
- A comparison of visual function tests in eyes with maculopathy. (1986) (45)
- Docosahexaenoic Acid Slows Visual Field Progression in X-Linked Retinitis Pigmentosa: Ancillary Outcomes of the DHAX Trial. (2015) (44)
- Rod phototransduction in retinitis pigmentosa. Distinguishing alternative mechanisms of degeneration. (1995) (43)
- Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa (2008) (43)
- Worldwide Argus II implantation: recommendations to optimize patient outcomes (2016) (43)
- Retinal degeneration in retinitis pigmentosa and neuronal ceroid lipofuscinosis: An overview. (1999) (42)
- Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3. (2003) (42)
- Dependence of cone b-wave implicit time on rod amplitude in retinitis pigmentosa (1987) (42)
- MACULAR ATROPHY IN BIRDSHOT RETINOCHOROIDOPATHY: An Optical Coherence Tomography and Multifocal Electroretinography Analysis (2010) (42)
- Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosa. (2009) (41)
- Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene. (2011) (41)
- A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy (2008) (40)
- Monocular light exclusion for a period of days reduces directional sensitivity of the human retina. (1979) (40)
- OUTCOME MEASURES AND THEIR APPLICATION IN CLINICAL TRIALS FOR RETINAL DEGENERATIVE DISEASES: Outline, Review, and Perspective (2005) (40)
- A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT. (2013) (40)
- Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5 (2017) (39)
- Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease (2019) (39)
- Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium (2020) (39)
- Functional Characterization of Mouse RDH11 as a Retinol Dehydrogenase Involved in Dark Adaptation in Vivo* (2005) (38)
- Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene. (2003) (38)
- Focal cone electroretinograms: Aging and macular disease (1988) (38)
- Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. (2001) (37)
- Retinal disease in mice lacking hypoxia-inducible transcription factor-2alpha. (2005) (37)
- Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3. (2017) (37)
- Red blood cell fatty acid levels in patients with autosomal dominant retinitis pigmentosa. (1993) (36)
- Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8 (2018) (34)
- North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene (2016) (33)
- Vitrectomy in Eyes at Risk for Macular Hole Formation (1990) (33)
- The focal electroretinogram in fellow eyes of patients with idiopathic macular holes. (1988) (31)
- Inferred positive phototropic activity in human photoreceptors. (1981) (31)
- Metabolism of omega-3 fatty acids in patients with autosomal dominant retinitis pigmentosa. (1995) (31)
- Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP). (2008) (31)
- Cone and rod ERG phototransduction parameters in retinitis pigmentosa. (2003) (31)
- Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7. (2011) (31)
- A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States (2017) (30)
- A double-blind placebo-controlled evaluation of the acute effects of sildenafil citrate (Viagra) on visual function in subjects with early-stage age-related macular degeneration. (2002) (30)
- Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients With Autosomal Dominant Retinitis Pigmentosa: A Randomized Phase 2 Multicenter Placebo-Controlled Clinical Trial (2018) (29)
- Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa (2017) (29)
- Effect of stimulus size on static visual fields in patients with retinitis pigmentosa. (2000) (29)
- Understanding changes in the b-wave of the ERG caused by heterogeneous receptor damage. (1994) (28)
- Heterogeneity in retinal disease and the computational model of the human-rod response. (1993) (27)
- Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa (2013) (27)
- Characterizing the phenotype and genotype of a family with occult macular dystrophy. (2012) (27)
- Diurnal rhythm in the human rod ERG. Relationship to cyclic lighting. (1986) (27)
- Functional analysis of vision in patients after retinal detachment repair. (1980) (27)
- De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy (2016) (27)
- Leveraging splice‐affecting variant predictors and a minigene validation system to identify Mendelian disease‐causing variants among exon‐captured variants of uncertain significance (2017) (27)
- Comparison of the Goldmann-Weekers Dark Adaptometer™ and LKC Technologies Scotopic Sensitivity Tester-1™ (2000) (27)
- Diagnosis of a mild peroxisomal phenotype with next-generation sequencing (2016) (26)
- ApoER2 Function in the Establishment and Maintenance of Retinal Synaptic Connectivity (2011) (26)
- Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity (2015) (25)
- Scotopic Microperimetric Assessment of Rod Function in Stargardt Disease (SMART) Study: Design and Baseline Characteristics (Report No. 1) (2018) (25)
- Rod visual fields in cone-rod degeneration. Comparisons to retinitis pigmentosa. (1990) (25)
- Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months (2018) (23)
- A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned (2019) (23)
- Safety assessment of docosahexaenoic acid in X-linked retinitis pigmentosa: the 4-year DHAX trial. (2014) (23)
- Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12. (2018) (23)
- Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa. (2019) (22)
- Reliability of a Manual Procedure for Marking the EZ Endpoint Location in Patients with Retinitis Pigmentosa (2016) (22)
- Next-generation sequencing to solve complex inherited retinal dystrophy: A case series of multiple genes contributing to disease in extended families (2017) (22)
- X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa. (2019) (22)
- Pupillometric measures of retinal sensitivity in infants and adults with retinitis pigmentosa (1987) (22)
- Visual phenotype in patients with Arg41Gln and Ala196+1bp mutations in the CRX gene (2000) (22)
- ω3 Fatty Acid Status in Patients with Retinitis pigmentosa (1998) (21)
- Operant acuity of toddlers and developmentally delayed children with low vision. (1987) (21)
- Vitrectomy in eyes at risk for macular hole formation. (1991) (20)
- Structure/Psychophysical Relationships in X-Linked Retinoschisis (2016) (20)
- Anomalous pigment epithelial photoreceptor relationships and receptor orientation. (1980) (20)
- Rod photoresponses in 6-week and 4-month-old human infants (1998) (19)
- CHOROIDEREMIA: Retinal Degeneration With an Unmet Need. (2019) (19)
- Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases (2021) (19)
- Cataract extraction after brachytherapy for malignant melanoma of the choroid. (1991) (19)
- Light reduction and the electroretinogram of preterm infants (1997) (19)
- Microperimetry for geographic atrophy secondary to age-related macular degeneration. (2019) (18)
- Survey: PNEUMATIC RETINOPEXY VERSUS SCLERAL BUCKLE: Preferences of Vitreous Society Members, 1990 (1992) (18)
- Metrics and Acquisition Modes for Fixation Stability as a Visual Function Biomarker (2017) (18)
- Interocular amplitude differences of the full field electroretinogram in normal subjects (2003) (17)
- Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene. (2005) (16)
- Rod ERGs in children with hereditary retinal degeneration. (1986) (16)
- The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1) (2018) (16)
- The effects of prolonged dark exposure on visual thresholds in young and adult rats. (1979) (16)
- Polymorphic variation of RPGRIP1L and IQCB1 as modifiers of X-linked retinitis pigmentosa caused by mutations in RPGR. (2012) (16)
- Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation with Other Measures of Disease Severity. (2020) (16)
- Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations (2019) (16)
- Submicrovolt full-field cone electroretinograms: artifacts and reproducibility (1996) (16)
- Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14. (2020) (16)
- Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers (2016) (16)
- Retinal Anatomy and Electrode Array Position in Retinitis Pigmentosa Patients After Argus II Implantation: An International Study. (2018) (16)
- The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline (2020) (16)
- Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation. (2004) (16)
- X-Linked Retinitis Pigmentosa: Current Status (2001) (15)
- Early abnormalities of rod function in children with X-linked retinitis pigmentosa (1993) (15)
- Evidence for alteration in photoreceptor orientation. (1980) (14)
- EVALUATION OF FULL-FIELD ELECTRORETINOGRAM REDUCTIONS AFTER OCRIPLASMIN TREATMENT (2017) (14)
- A randomized placebo-controlled clinical trial of docosahexaenoic acid (DHA) supplementation for X-linked retinitis pigmentosa. (2005) (14)
- Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13. (2020) (13)
- Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies. (2015) (13)
- Psychophysical studies of cone optical bandwidth in patients with retinitis pigmentosa (1982) (13)
- Electroretinographic determination of human rod flash response in vivo. (2000) (12)
- Persistent cone dysfunction in acute exudative polymorphous vitelliform maculopathy. (2007) (12)
- Rod transduction parameters from the a wave of local receptor populations. (1995) (12)
- Pattern-reversal electroretinographic acuity in untreated eyes with subfoveal neovascular membranes. (1992) (12)
- Randomised study evaluating the pharmacodynamics of emixustat hydrochloride in subjects with macular atrophy secondary to Stargardt disease (2020) (12)
- Application of a Deep Machine Learning Model for Automatic Measurement of EZ Width in SD-OCT Images of RP (2020) (11)
- Macular spatial distribution of preserved autofluorescence in patients with choroideremia (2018) (11)
- Five novel RPGR mutations in families with X‐linked retinitis pigmentosa (2001) (11)
- Retinal Sensitivity Using Microperimetry in Age-Related Macular Degeneration in an Amish Population. (2019) (11)
- Significance of ω3 Fatty Acids for Retinal and Brain Development of Preterm and Term Infants1 (1994) (11)
- Diurnal rhythm in the human rod ERG: retinitis pigmentosa. (1987) (10)
- Omega 3 fatty acid status in patients with retinitis pigmentosa. (1998) (10)
- LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS—SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED (2021) (10)
- Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1) (2020) (10)
- Reliability of Semiautomated Kinetic Perimetry (SKP) and Goldmann Kinetic Perimetry in Children and Adults With Retinal Dystrophies (2019) (9)
- An early nonsense mutation facilitates the expression of a short isoform of CNGA3 by alternative translation initiation (2018) (9)
- Survey: Current Popularity of Pneumatic Retinopexy (1999) (9)
- Visual Function and the Essentiality of α-Linolenic Acid and Docosahexaenoic Acid in Human Infants (1997) (9)
- Rod photoreceptor temporal properties in retinitis pigmentosa. (2011) (9)
- Histopathologic Assessment of Optic Nerves and Retina From a Patient With Chronically Implanted Argus II Retinal Prosthesis System (2019) (9)
- Computational models of rod-driven retinal activity (1995) (9)
- Outer Segment Thickness Predicts Visual Field Response to QLT091001 in Patients with RPE65 or LRAT Mutations. (2015) (8)
- Surrogate electroretinographic markers for assessing therapeutic efficacy in the retina (2004) (8)
- Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial (2016) (8)
- Phase 1, Dose-Escalating Study of the Safety, Tolerability, and Pharmacokinetics of ACU-4429 in Healthy Volunteers (2009) (8)
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- The Gly 56 Arg mutation in NR 2 E 3 accounts for 1-2 % of autosomal dominant retinitis pigmentosa (2007) (6)
- Longitudinal measures in children receiving ENCAD for hereditary retinal degeneration (2004) (6)
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- A novel splice site mutation in the gene for peripherin/RDS causing dominant retinal degeneration (1996) (6)
- A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia (2020) (6)
- Effect of Human Central Nervous System Stem Cell Subretinal Transplantation on Progression of Geographic Atrophy Secondary to Non Neovascular Age-Related Macular Degeneration. (2020) (5)
- Essential Fatty Acids in Visual and Brain Dev e l o p m e n t (2001) (5)
- Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP. (2003) (5)
- Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q. (2000) (5)
- Natural History of Progression of Choroideremia (NIGHT) Study: Cross-Sectional Analysis of Baseline Characteristics (2018) (5)
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- A Phase 1 Open-Label, Non-Comparative Study Evaluating the Safety of a Single, Unilateral Subretinal Administration of CNTO2476 (Human Umbilical Tissue-Derived Cells [hUTC]) in Advanced Retinitis Pigmentosa (RP) (2010) (4)
- The Natural History of the Progression of Choroideremia (NIGHT) Study: Longitudinal Changes in Visual Acuity over 12 Months (2018) (4)
- Recent Results from Second Sight’s Argus® II Retinal Prosthesis Study (2013) (4)
- Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1 (2020) (4)
- Diurnal variations of foveoschisis by optical coherence tomography in patients with RS1 X-linked juvenile retinoschisis (2018) (4)
- Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome (2021) (3)
- Topography of Rod and Cone Sensitivity Loss in Retinitis Pigmentosa (1997) (3)
- A Hybrid Model Composed of Two Convolutional Neural Networks (CNNs) for Automatic Retinal Layer Segmentation of OCT Images in Retinitis Pigmentosa (RP) (2021) (3)
- Four-Year Outcomes from a Randomized Clinical Trial of Docosahexaenoic Acid (DHA) Supplementation in X-Linked Retinitis Pigmentosa (XLRP) (2003) (3)
- Adaptation to polarized light in humans (1982) (3)
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- Linkage Mapping in Families With Autosomal Dominant Retinitis Pigmentosa (adRP) (2005) (3)
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- Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness (2012) (3)
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- Erratum to: Worldwide Argus II implantation: recommendations to optimize patient outcomes (2016) (3)
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- Maturation of visual and mental function in 18-month old infants receiving dietary long-chain polyunsaturated fatty acids (2003) (2)
- A Comparison of the Medmont Dark Adapted Chromatic Perimeter (DAC) with the Full-Field Stimulus Threshold (FST) in Subjects with Retinitis Pigmentosa (RP) (2016) (2)
- Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy (2020) (2)
- Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation with Disease Severity. (2022) (2)
- Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in X-linked Retinoschisis - 1 Year Clinical Results. (2022) (2)
- VALIDATION OF A DEEP LEARNING-BASED ALGORITHM FOR SEGMENTATION OF THE ELLIPSOID ZONE ON OPTICAL COHERENCE TOMOGRAPHY IMAGES OF AN USH2A-RELATED RETINAL DEGENERATION CLINICAL TRIAL (2022) (2)
- Natural History of the Progression of RPGR-Associated X-Linked Retinitis Pigmentosa (XOLARIS) Study: Cross-Sectional Analysis of Baseline Characteristics (2019) (2)
- Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium (2021) (2)
- Quantification of RPE Changes in Choroideremia Using a Photoshop-Based Method (2020) (2)
- Progressive Loss of Rod Sensitivity in Patients with Autosomal Dominant Retinitis Pigmentosa (adRP) due to RHO Pro23His Mutation (2017) (2)
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- Rod Ergs in Mice and Humans with Putative Null Mutations in the RDS Gene (1997) (2)
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- Area Measurement of the Ellipsoid Zone (EZ) by SD-OCT and its Correlation with Visual Field Identifies a Potential Anatomical Endpoint for Clinical Trials in Retinitis Pigmentosa (RP) (2014) (1)
- DOCOSAHEXAENOIC ACID ABNORMALITIES IN RED BLOOD CELLS OF PATIENTS WITH RETINITIS PIGMENTOSA (1995) (1)
- Clinical Characterization of RP11 in Five Families With Identified PRPF31 Mutations (2006) (1)
- Intraocular Sustained Release of CNTF Affects fdOCT Measures of Photoreceptor Function in Patients With Retinitis Pigmentosa (2010) (1)
- In-utero and post-delivery supplementation of motor neuron degeneration mutant mice with polyunsaturated fatty acids does not alter the clinical or pathological course. (1997) (1)
- RNA-based therapies in inherited retinal diseases (2022) (1)
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- FdOCT Analysis Of The Transition Zone Between Healthy And Severely Affected Regions In Patients With Choroideremia (2011) (1)
- Ancillary Outcomes of the DHAX Trial: Docosahexaenoic Acid (DHA) Supplementation in X-Linked Retinitis Pigmentosa (XLRP) (2015) (1)
- Evaluation of Inner Retinal Layers in Patients with Retinitis Pigmentosa Using Optical Coherence Tomography (2013) (1)
- Retinal Targeted-Capture Next Generation Sequencing and CLIA Confirmation in a Representative Range of Patients with Inherited Retinal Degeneration (2015) (1)
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- Application of Whole-Exome and Retinal-Capture Next-Generation DNA Sequencing to Identify Disease-Causing Mutations in Families with a Diagnosis of Autosomal Dominant Retinitis Pigmentosa (2013) (1)
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- Mutations in IMPDH1 Are Associated With Leber Congenital Amaurosis (2005) (1)
- Frequency and Spectrum of IMPDH1 Mutations Associated with Autosomal Dominant Retinitis Pigmentosa (2003) (1)
- Analysis of protein haplotypes in trans as factors modifying phenotypic variation of retinal dystrophies caused by a splice site mutation in the peripherin/RDS gene (2004) (1)
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- Comparison of Kinetic Visual Fields (Goldmann and Octopus) and Threshold Visual Fields (Octopus macular static and Full-Field Stimulus Threshold) in Patients with Inherited Retinal Diseases (2014) (1)
- Generation of Homozygous Stargardt-3 Mice Which Completely Lack Retinal Polyunsaturated C28-C36 Fatty Acids (2010) (1)
- Safety Assessment of High Dose Docosahexaenoic Acid (DHA) Supplementation in a 4-Year Randomized Clinical Trial in X-linked Retinitis Pigmentosa (XLRP) (2002) (1)
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- Identification of mutations in three retinal dystrophy genes within a single family: PRPF8, PRPH2 and USH2A (2015) (1)
- Abnormal Retinal Morphology and Function in Homozygous Stargardt-3 Mice Which Completely Lack Polyunsaturated C28-C36 Fatty Acids in the Mature Retina (2010) (1)
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- Long-term follow-up of patients with retinitis pigmentosa (RP) receiving sustained-release CNTF through intraocular encapsulated cell technology implants (2013) (1)
- Annual decline in visual sensitivity at the edge of the OCT-defined ellipsoid zone (EZ) in patients with RPGR-mediated x-linked Retinitis Pigmentosa (xlRP) (2014) (1)
- Autosomal dominant retinitis pigmentosa: exclusion of known and mapped genes in three families. (2004) (1)
- Month 18 changes in microperimetric mean sensitivity, fixation location, and fixation stability in Stargardt disease: The ProgStar Study (2017) (1)
- Genome-Wide Linkage Analysis For Gene Discovery In Autosomal Dominant Retinitis Pigmentosa (2012) (1)
- Phenotypic Characterization Of Three Families With Autosomal Dominant Retinitis Pigmentosa (adRP) Due To Mutations In KLHL7 (2011) (0)
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- Microperimetry fixation characteristics in an Amish Population with Age-Related Macular Degeneration (2018) (0)
- EZ Width Reflects Disease Severity in adRP Patients with PRPF31 Gene Mutations (2017) (0)
- PNAS Plus Significance Statements (2015) (0)
- Generation of a Gene–Knockin Mouse Model of Stargardt–3 Macular Dystrophy (2006) (0)
- A novel SVA retrotransposon insertion in CHM results in loss of REP-1 protein causing choroideremia (2019) (0)
- Optical delivery and broadband activation of polychromatic opsin lowers intensity threshold for photostimulation (2015) (0)
- New Developments in Vision Research A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies : Findings and Lessons Learned (2019) (0)
- Pediatric Hereditary Macular Degenerations (2011) (0)
- Rod visual fields in comparison to the recommended functional and structural screening tests for patients treated with hydroxychloroquine (2020) (0)
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- Comparison of Visual Field Boundaries to Loci of fdOCT Receptor Loss in Patients with RP (2011) (0)
- Interocular Comparisons of Progression Following Uniocular Fundus Photography and Full-Field ERG in Patients With Retinitis Pigmentosa (RP) Due to Rhodopsin Mutations (2007) (0)
- Detectable rod function in patients with retinitis pigmentosa (RP) with or without a measureable rod electroretinogram (ERG) response (2016) (0)
- Mutations in X-Linked RPGR in Families With Apparent Autosomal Dominant Retinitis Pigmentosa (adRP) (2003) (0)
- Severe Early-onset LCA-like Retinal Dystrophy due to Compound Heterozygous PRPH2 Mutations (2015) (0)
- Scotopic and Mesopic Retinal Sensitivity in Age-Related Macular Degeneration in an Amish Population (2016) (0)
- Retinal Nerve Fiber Layer Thickness in Patients With Retinitis Pigmentosa (2009) (0)
- Mechanistic Studies of AIPL1-Rod cGMP Phosphodiesterase (PDE6) Interaction (2008) (0)
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- Dietary Nutrients and Yearly Rates of Decline in Retinal Function in Patients with X-linked Retinitis Pigmentosa (XLRP) (2003) (0)
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- The role of electrophysiology in detecting and following retinal dystrophies (2010) (0)
- Retinitis pigmentosa affects cone phototransduction as well as post-synaptic cone activity (1995) (0)
- Central Rod and Cone A–Wave Parameters in Macular Forms of Photoreceptor Degeneration (2005) (0)
- Asymmetric maculopathy with mutations in adenosine triphosphate-binding cassette, sub-family A, member 4 and jagged canonical notch ligand 1 after 30 years of monocular aphakia (2021) (0)
- Clinical Characterization of RP10 in a Large Family With an Identified (Asp226Asn) IMPDH1 Mutation (2005) (0)
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- Prolonged Rod Visual Cycle Suppression with ACU-4429 in Patients with Geographic Atrophy (2012) (0)
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- Factors Modifying Severity and Penetrance in Males and Females with Retinitis Pigmentosa Caused by Mutations in the X-Linked RPGR Gene (2012) (0)
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- Using Peripheral Blood Leukocytes to Detect PRPF31 Haploinsufficiency (2008) (0)
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- Structure - Function Correlates in the Retina Surrounding Geographic Atrophy (GA): A Comparison Study of Peri-GA Scotopic Sensitivities and Retinal Anatomic Parameters (2012) (0)
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- Paired-flash electroretinography: a new tool to examine rod function in patients with Stargardt disease (2002) (0)
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- Light Adaptation and Post-Flash Recovery in Human Rods (1995) (0)
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- Disease-causing mutations in a cohort of autosomal dominant RP (adRP) families without detectable mutations in known adRP genes (2015) (0)
- Genetic Testing Adds Research and Clinical Value to a Retinal Degeneration Registry (2018) (0)
- FdOCT Analysis of the Transition Zone Between Healthy and Severely Affected Regions in Patients With Retinitis Pigmentosa (RP) (2010) (0)
- RP2 Mutations Cause Variable Phenotypes in Carrier Females in Two Families With Retinitis Pigmentosa (2010) (0)
- Randomized clinical trial evaluating the pharmacodynamics of emixustat in subjects with macular atrophy secondary to Stargardt disease (2020) (0)
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- A Screen for Genomic Rearrangements in Genes Known to Cause Autosomal Dominant Retinitis Pigmentosa (AdRP) (2007) (0)
- Characterizing the Phenotype and Genotype of Families with Occult Macular Dystrophy (2012) (0)
- Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease (2019) (0)
- Improvement in baseline amplitude of the scotopic b-wave after release of vitreomacular traction (VMT): Further substudy analysis from the OASIS trial (1) (2017) (0)
- Progression of atrophic lesions prospectively determined by fundus autofluorescence: the natural history of the progression of atrophy secondary to Stargardt disease (ProgStar) study (2016) (0)
- Optical Coherence Tomography in Patients Diagnosed with North Carolina Macular Dystrophy N (0)
- Heparin Enhances AAV2–mediated Transduction Efficiency In The Mouse Retina (2004) (0)
- Baseline visual fields in the RUSH2A study: Associated factors and correlation with measures of disease severity (2020) (0)
- Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements (2013) (0)
- Natural progression of scotopic and photopic macular function loss in patients with Stargardt disease: The SMART Study. (2017) (0)
- Electroretinographic Testing in Infants and Children (2011) (0)
- Diurnal Rhythm in the ROD ERG in Retinitis Pigmentosa and CONE-ROD Degeneration (1987) (0)
- Rod a-wave as a measure of rod receptor activity: cone intrusion can influence estimated parameters (1993) (0)
- RP1 Mutation Analysis (2001) (0)
- Five Novel RPGR Mutation in brief: Mutations in Families with XLinked Retinitis Pigmentosa (2000) (0)
- Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence (2023) (0)
- Quantification of RPE changes in choroideremia using a Photoshop-based protocol (2019) (0)
- S-cone ERGs and S-cone acuity in patients with retinitis pigmentosa (RP) (1992) (0)
- A Novel GCAP1 Mutation Linked to Dominant Cone Dystrophy (2007) (0)
- Analysis of visual acuity and cyst volume measurements in a natural history study in X-Linked Retinoschisis (XLRS) (2015) (0)
- Deep learning-based automatic segmentation of intact ellipsoid zone area on optical coherence tomography images of USH2A-related retinal degeneration (2020) (0)
- Natural History and Effect of Carbonic Anhydrase Inhibitor Use in X-Linked Retinoschisis (2017) (0)
- Rod and Cone Contributions to fdOCT Measures of Photoreceptor Structure in Retinal Degenerative Diseases (2011) (0)
- CLINICAL CHARACTERIZATION OF DISEASE SEVERITY AND PROGRESSION IN X–LINKED RETINITIS PIGMENTOSA (XLRP) ASSOCIATED WITH RPGR MUTATIONS: (2004) (0)
- SAG (S-antigen visual arrestin-1) mutations cause autosomal dominant retinitis pigmentosa (adRP) without the Oguchi disease phenotype (2017) (0)
- Scotopic and photopic macular functions as assessed with microperimetry (MP1) in patients with Stargardt disease type 1 – The SMART Study (2016) (0)
- Rod and cone a–wave parameters from the central retina (2004) (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)
- ERGs and VEPs in Very Low Birth Weight (VLBW) Infants (1988) (0)
- FdOCT Measures Of Progression Over A One Year Interval In Patients With X-linked Retinitis Pigmentosa (XLRP) (2011) (0)
- A Comparison of Local Multifocal Electroretinograms (mfERG) to Local OCT Receptor Thicknesses in Retinitis Pigmentosa (RP) (2011) (0)
- The Rate of Progressive Loss of Shape Discrimination Hyperacuity and Visual Acuity in Stargardt Macular Dystrophy (2009) (0)
- Measures of Static Perimetric Field Progression in Retinitis Pigmentosa (2005) (0)
- Within-visit And Between-visit Repeatability Of The Diagnosys Full-field Stimulus Threshold (D-FST) When Measuring Rod Sensitivity In Patients With Atrophic Age-related Macular Degeneration (ARMD) (2012) (0)
- The Relationship of Choroidal Thickness to Scotopic Sensitivity in Age-related Macular Degeneration (AMD) (2013) (0)
- The Intensity of Outer Retinal Layers Seen on Frequency Domain OCT in Patients with Outer Retinal Disease (2012) (0)
- Test-retest variability on the Medmont dark-adapted chromatic (DAC) perimeter in controls and patients with inherited retinal disease (IRD) (2018) (0)
- Progression in Patients with Advanced Retinal Degenerative diseases (RDD) followed with Full-field Stimulus Threshold (FST) Testing (2014) (0)
- TrkB Receptor Delivered by Adeno–Associated Viruses Delays Photoreceptor Degeneration in Rhodopsin Knockout Mice (2005) (0)
- Variability Of Full-field Erg In A Population Without Diffuse Photoreceptor Cell Disease (2002) (0)
- The Role of ApoER2 Exon19 Splicing in Retinal Degeneration (2008) (0)
- Static and dynamic assessment of fixation stability in Stargardt disease (2018) (0)
- Disease-causing Copy Number Variants (CNVs) in Genes Associated With Autosomal Recessive Retinal Degeneration (2009) (0)
- Assessment of Phenotypic Variability Among Female Carriers of X-linked Retinitis Pigmentosa (xlRP) due to RPGR Mutations (2011) (0)
- Fundus Appearance in X-linked Retinitis Pigmentosa (XLRP) Over a 4-Year-Interval (2002) (0)
- The Relationship Between ERG Measures of Phototransduction Efficiency and Genotype in Retinitis Pigmentosa (2003) (0)
- Rapid Clinical Assessment of A-Wave Photoreceptor Function (2003) (0)
- Results from spectral-domain optical coherence tomography (SD-OCT) at baseline compared with normative data: The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study (2016) (0)
- Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2 (2022) (0)
- Effect of stimulus size on automated static visual fields from patients with retinitis pigmentosa (1999) (0)
- The cone outer segment termination (COST) line appears abnormal on OCT scans of patients with stationary and progressive forms of cone dysfunction (2013) (0)
- Caveolin–1 Null Mice Have Reduced Retinal Function Without Overt Retinal Degeneration (2006) (0)
- Evaluation of full-field electroretinogram changes after ocriplasmin injection in a substudy of symptomatic vitreomacular adhesion subjects from the OASIS trial (2016) (0)
- The Transcription Factor PRDM8 Is Required for Rod and Cone Bipolar Cell Maintenance (2007) (0)
- Local and global visual function deficits in patients with ABCR gene mutations (2000) (0)
- Assessment of Everyday Visual Tasks in Carriers of X-Linked Retinitis Pigmentosa: Use of the Visual Activities and Low Luminance Questionnaires (2010) (0)
- Docosahexaenoic Acid Profiles in Red Blood Cells of Patients With Retinal Degenerative Diseases (2007) (0)
- Rates of Decline in fdOCT Defined Regions of the Visual Field in Patients with RPGR-mediated X-Linked Retinitis Pigmentosa (XLRP) (2015) (0)
- Polymorphic Variation in RPGRIP1 and RPGRIP1L as Potential Modifiers of X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR (2010) (0)
- Microenvironment Function Due to Disturbance of Subretinal Loss of Caveolin-1 Impairs Retinal Neurobiology : (2012) (0)
- Threshold versus Area Assessment to Determine Aspects of Rod Photoreceptor Loss in Subjects with Age-Related Macular Degeneration (AMD). (2016) (0)
- The Diagnosys Full-Field Stimulus Threshold (d-fst) Is a Useful Tool to Assess Visual Function in Low Vision Subjects (2009) (0)
- Prevalence of Mutations in TOPORS Causing Autosomal Dominant Retinitis Pigmentosa (adRP) (2008) (0)
- A tandem duplication of PRDM13 in a family with North Carolina Macular Dystrophy (MCRD1) (2016) (0)
- SNRNP200 Mutations Account for 2% of Autosomal Dominant Retinitis Pigmentosa (2013) (0)
- The Inhibitory Effect of CNTF on Retinal Function: Mediation by bFGF (2006) (0)
- SD-OCT May Predict Response to QLT091001 in Patients with LCA or RP associated with RPE65 or LRAT Mutations (2013) (0)
- Photoreceptor alignment. (1985) (0)
- Novel Mutations Identified in a Screen of Patients With Autosomal Dominant Retinitis Pigmentosa (2003) (0)
- Argus II Retinal Prosthesis System Post-Approval US Cohort 1 Year Outcomes (2017) (0)
- A Comparison of Methods For Tracking Progression in Patients with X-Linked Retinitis Pigmentosa Using Frequency Domain OCT (2013) (0)
- Loss of Cone and Reduction in Rod ERG Responses in the Guanylyl Cyclase-E (GC-E) Deficient Mouse (1999) (0)
- An evaluation of the ERG b-wave as a measure of inner nuclear layer activity: Implications for Naka-Rushton fits (1991) (0)
- The progression of Stargardt Disease as determined by fundus autofluorescence over a 24-month period (ProgStar Report No. 17). (2023) (0)
- Reliability of a Manual Procedure for Marking the EZ Band Endpoint Location (2015) (0)
- Rod-mediated Sensitivity Loss Precedes SD-OCT Thickness Changes in the Outer Retina of Senior Patients with Intermediate Size Drusen (2012) (0)
- Absence of Transcription Factor Prdm8 Leads to Stationary Night Blindness in Mice (2007) (0)
- Human mutant ELOVL4 causes retinal dystrophy in transgenic mice (2004) (0)
- Does the Complement Factor H (CFH) Tyr402His Polymorphism Affect the Retinal Phenotype of a Clinically Variable RDS Mutation (2007) (0)
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What Schools Are Affiliated With David G. Birch?
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