Citation Impact
Citing Papers
Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2
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Diffuse Axonal and Tissue Injury in Patients With Multiple Sclerosis With Low Cerebral Lesion Load and No Disability
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Optical coherence tomography angiography
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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
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The Retinal Pigment Epithelium in Visual Function
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Chronic cerebrospinal venous insufficiency in patients with multiple sclerosis
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Population frequencies of inherited neuromuscular diseases—A world survey
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G Protein-Coupled Receptor Kinase Function Is Essential for Chemosensation in C. elegans
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Why cotton wool spots should not be regarded as retinal nerve fibre layer infarcts
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Classical and new roles of β-arrestins in the regulation of G-PROTEIN-COUPLED receptors
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BREAKDOWN OF THE BLOOD-BRAIN BARRIER PRECEDES SYMPTOMS AND OTHER MRI SIGNS OF NEW LESIONS IN MULTIPLE SCLEROSIS
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Rab escort protein 1 (REP1) in intracellular traffic: a functional and pathophysiological overview
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Genetik des Usher-Syndroms
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The epidemics of myopia: Aetiology and prevention
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Standard Diagnostic Criteria for the Acute Retinal Necrosis Syndrome
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Facioscapulohumeral muscular dystrophy
2006
Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa
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An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy
2000
Common synonymous variants in ABCA4 are protective for chloroquine induced maculopathy (toxic maculopathy)
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Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele
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Unraveling A Complex Genetic Disease: Age-related Macular Degeneration
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Divergence Insufficiency Revisited<subtitle>Natural History of Idiopathic Cases and Neurologic Associations</subtitle>
2000
Microvascular Abnormality in Relapsing-Remitting Multiple Sclerosis: Perfusion MR Imaging Findings in Normal-appearing White Matter
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Prevalence of Muscular Dystrophies: A Systematic Literature Review
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Multi-Ethnic Study of Atherosclerosis: Objectives and Design
2002 Standout
Normal rat serum cytotoxicity against syngeneic oligodendrocytes
1989
Antibodies to myelin oligodendrocyte glycoprotein are not involved in the severity of chronic non-remitting experimental autoimmune encephalomyelitis
2008 StandoutNobel
Pathogenesis of multiple sclerosis
1994
Eye and Kidney
2003
Wnt/β-Catenin Signaling and Disease
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Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases
2009 Standout
The Role of Oxidative Stress in the Pathogenesis of Age-Related Macular Degeneration
2000 Standout
X-linked Retinitis Pigmentosa Profile of Clinical Findings
1988
Retinitis pigmentosa
2006 Standout
N-Acetylaspartate in the CNS: From neurodiagnostics to neurobiology
2007 Standout
Vascular Endothelial Growth Factor in Ocular Fluid of Patients with Diabetic Retinopathy and Other Retinal Disorders
1994 Standout
Leber congenital amaurosis: Genes, proteins and disease mechanisms
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A Randomized, Placebo-Controlled Trial of Natalizumab for Relapsing Multiple Sclerosis
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Hypoperfusion predicts lesion progression in cerebral X-linked adrenoleukodystrophy
2012
A model for familial exudative vitreoretinopathy caused by LPR5 mutations
2008 StandoutNobel
Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q
2004
Purification of component A of Rab geranylgeranyl transferase: Possible identity with the choroideremia gene product
1992 StandoutNobel
Müller cells in the healthy and diseased retina
2006 Standout
The β subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dysplasia 1
1992
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
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Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
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Abnormal Supranuclear Eye Movements in the Child
2000
Ranibizumab for Macular Edema following Central Retinal Vein Occlusion
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Recommendations on Screening for Chloroquine and Hydroxychloroquine Retinopathy (2016 Revision)
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Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia
2003 Standout
The Pathobiology of Vascular Dementia
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X-Linked Recessive Atrophic Macular Degeneration from RPGR Mutation
2002
VEGF in Signaling and Disease: Beyond Discovery and Development
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Age-related Macular Degeneration
1998
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
2005
Animal models
1994
The epidemiology of age-related macular degeneration
2004
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
2001
Retinitis Pigmentosa
1999
Identification of a novel protein interacting with RPGR
2000
The Fibroblast Growth Factor signaling pathway
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Vascular endothelial growth factor and ocular neovascularization.
1997
The Importance of the Omega-6/Omega-3 Fatty Acid Ratio in Cardiovascular Disease and Other Chronic Diseases
2008 Standout
Natural History of Choroidal Neovascularization in Degenerative Myopia
1984
Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man
1998
Cerebellar saccadic dysmetria is not equal in the two eyes
1983
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
2000
Isolation of a candidate gene for choroideremia.
1992
Ocular Neovascularization with Retinal Vascular Occlusion-III
1983
Autosomal Dominant Vitreoretinochoroidopathy
1982
Pathophysiology of age-related macular degeneration
1987
Ischemic Retinal Vasculitis and Its Management
2014
Experimental autoimmune panencephalitis and uveoretinitis transferred to the Lewis rat by T lymphocytes specific for the S100 beta molecule, a calcium binding protein of astroglia.
1994
Effects of induced hyperthermia on visual evoked potentials and saccade parameters in normal subjects and multiple sclerosis patients.
1980
IMMUNOLOGY OF MULTIPLE SCLEROSIS
2005 Standout
Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms
1995 Standout
Standardization of Uveitis Nomenclature for Reporting Clinical Data. Results of the First International Workshop
2005 Standout
Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
2000
The Usher syndromes
1999
Pigment Epithelium-Derived Factor Supports Normal Development of Photoreceptor Neurons and Opsin Expression after Retinal Pigment Epithelium Removal
2000
THE WNT SIGNALING PATHWAY IN DEVELOPMENT AND DISEASE
2004 Standout
Diagnostic criteria for idiopathic intracranial hypertension
2002 Standout
Evoked Potentials in Clinical Medicine
1982 Standout
Metastatic bacterial endophthalmitis: A contemporary reappraisal
1986
Bacillus cereus and related species
1993 Standout
Histopathologic Study of Nine Branch Retinal Vein Occlusions
1982
Nonlinear neural networks: Principles, mechanisms, and architectures
1988 Standout
Central retinal vein occlusion: a prospective histopathologic study of 29 eyes in 28 cases.
1981
Mildly abnormal retinal function in transgenic mice without Müller cell aquaporin-4 water channels.
2002
Genes and mutations causing retinitis pigmentosa
2013 Standout
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.
1989
Works of A.C. Bird being referenced
X-linked retinitis pigmentosa.
1974
5-year Incidence of Age-related Maculopathy - Reykjavik Eye Study
2003
Multi-Focal ERG, Pattern ERG and Psychophysical Correlates of Fundus Autofluorescence Abnormalities in Patients With Retinitis Pigmentosa
2003
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy
2007
The contribution of USH1C mutations to syndromic and non‐syndromic deafness in the UK
2003
Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
1997
Krill's Hereditary Retinal and Choroidal Diseases
1978
RETINAL VENOUS SHEATHING IN OPTIC NEURITIS
1987
Bilateral acute retinal necrosis.
1978
Further refinement of the Usher 2A locus at 1q41.
1998
Histopathological and biochemical studies on donor eyes affected with retinitis pigmentosa.
1987
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16 (vol 5, pg 1055, 1996)
1996
New genetic loci and gene mutations in X-linked retinal disease
1999
Internuclear ophthalmoplegia. An electro-oculographic study of peak angular saccadic velocities.
1976
RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY
1987
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.
1996
Experimental retinal branch vein occlusion in rhesus monkeys. I. Clinical appearances.
1979
Stickler's syndrome and neovascular glaucoma.
1979
Autosomal dominant exudative vitreoretinopathy.
1980
Divergence paralysis with raised intracranial pressure. An electro-oculographic study.
1972
A histopathologic study of a choroideremia carrier.
1990
Retinal Telangiectasis in Facioscapulohumeral Muscular Dystrophy With Deafness
1985