Citation Impact
Citing Papers
rMATS: Robust and flexible detection of differential alternative splicing from replicate RNA-Seq data
2014 Standout
Complement Factor H Polymorphism and Age-Related Macular Degeneration
2005 StandoutScience
Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration
2005 StandoutScience
Complement Factor H Polymorphism in Age-Related Macular Degeneration
2005 StandoutScience
Drusen associated with aging and age‐related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease
2000
Reconsidering Movement of Eukaryotic mRNAs between Polysomes and P Bodies
2011 StandoutNobel
TIMP-3 Binds to Sulfated Glycosaminoglycans of the Extracellular Matrix
2000
Optical coherence tomography angiography
2017 Standout
Mutations in PRPF31 Inhibit Pre-mRNA Splicing of Rhodopsin Gene and Cause Apoptosis of Retinal Cells
2005
The multifunctional choroid
2009 Standout
The Retinal Pigment Epithelium in Visual Function
2005 Standout
Mass spectrometric analysis of the human 40S ribosomal subunit: Native and HCV IRES‐bound complexes
2005 StandoutNobel
PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor
2004
Pre-mRNA splicing and human disease
2003
Up-Regulation of Glial Fibrillary Acidic Protein in Response to Retinal Injury: Its Potential Role in Glial Remodeling and a Comparison to Vimentin Expression
2003
Fundus autofluorescence and age-related macular degeneration
2003
Structure and composition of drusen associated with glomerulonephritis: Implications for the role of complement activation in drusen biogenesis
2001
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas
2009 Standout
Age-Related Macular Degeneration
2008 Standout
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Comprehensive proteomic analysis of the human spliceosome
2002 Nature
The Spliceosome: Design Principles of a Dynamic RNP Machine
2009 Standout
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle
2008
Light in retinitis pigmentosa
2004
Generation of retinal cells from mouse and human induced pluripotent stem cells
2009 StandoutNobel
The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors
2000
Pegaptanib, a targeted anti-VEGF aptamer for ocular vascular disease
2006 Standout
Age-Related Macular Degeneration: Etiology, Pathogenesis, and Therapeutic Strategies
2003
Transcript Specificity in Yeast Pre-mRNA Splicing Revealed by Mutations in Core Spliceosomal Components
2007
Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
2015 Standout
Angiogenesis in health and disease
2003 Standout
Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions
2007
Complement: a key system for immune surveillance and homeostasis
2010 Standout
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
NEW EMBO MEMBER'S REVIEW: On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
2002
Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
2002
Renewal of photoreceptor outer segments and their phagocytosis by theretinal pigment epithelium
2000
Idiopathic Intracranial Hypertension
2010
An Integrated Hypothesis That Considers Drusen as Biomarkers of Immune-Mediated Processes at the RPE-Bruch's Membrane Interface in Aging and Age-Related Macular Degeneration
2001
The Hippo Signaling Pathway in Development and Cancer
2010 Standout
Aptamers as therapeutics
2010 Standout
Autologous Translocation of the Choroid and Retinal Pigment Epithelium in Age-related Macular Degeneration
2006
TEAD mediates YAP-dependent gene induction and growth control
2008 Standout
Retinitis pigmentosa
2006 Standout
A Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human Dysmorphism
2017 StandoutNobel
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
2006
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Expansion of the eukaryotic proteome by alternative splicing
2010 StandoutNature
A Novel TIMP-3 Mutation Reveals a Common Molecular Phenotype in Sorsby's Fundus Dystrophy
2000
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes
2016
Matrix metalloproteinases as modulators of inflammation and innate immunity
2004 Standout
Age-related macular degeneration
2018 Standout
Understanding age-related macular degeneration (AMD): Relationships between the photoreceptor/retinal pigment epithelium/Bruch’s membrane/choriocapillaris complex
2012
Circular RNAs are abundant, conserved, and associated with ALU repeats
2012 Standout
Aging and vision
2010 Standout
A Genome-Wide Analysis Indicates that Yeast Pre-mRNA Splicing Is Predominantly Posttranscriptional
2006 StandoutNobel
Aging, age-related macular degeneration, and the response-to-retention of apolipoprotein B-containing lipoproteins
2009
Müller cells in the healthy and diseased retina
2006 Standout
Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs
2009
Retinal and choroidal angiogenesis: pathophysiology and strategies for inhibition
2003
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay
2008
A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2
2003
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
2002
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)
2004
The epidemiology of retinitis pigmentosa in Denmark
2002
Towards an understanding of age-related macular disease
2003
Prp8 protein: At the heart of the spliceosome
2005
Subtractive Hybridization of mRNA from early passage and senescent endothelial cells
2000
Distribution and composition of esterified and unesterified cholesterol in extra-macular drusen
2007
A role for local inflammation in the formation of drusen in the aging eye
2002
Molecular Architecture of the Human Pre-mRNA 3′ Processing Complex
2009 StandoutNobel
Intravitreal Bevacizumab (Avastin) for Neovascular Age-Related Macular Degeneration
2006 Standout
FUNDUS AUTOFLUORESCENCE IMAGING
2008
Magnetic resonance imaging in pseudotumor cerebri
1998
Pathogenesis of lesions in late age-related macular disease
2004
Molecular genetics of macular degeneration
2001
Expression of Sorsby's Fundus Dystrophy Mutations in Human Retinal Pigment Epithelial Cells Reduces Matrix Metalloproteinase Inhibition and May Promote Angiogenesis
2002
Indocyanine Green Angiographic Features of Pathologic Myopia
1996
Prevalence and Morphology of Druse Types in the Macula and Periphery of Eyes with Age-Related Maculopathy
2008
Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa.
2008
Vitronectin is a constituent of ocular drusen and the vitronectin gene is expressed in human retinal pigmented epithelial cells
1999
Global gene expression of cells attached to a tissue engineering scaffold
2004 StandoutNobel
The Senescence-Associated Secretory Phenotype: The Dark Side of Tumor Suppression
2010 Standout
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
2005 Standout
Binding of the Human Prp31 Nop Domain to a Composite RNA-Protein Platform in U4 snRNP
2007 Science
Mass spectrometry-based proteomics
2003 StandoutNature
Functional redundancy of cryptochromes and classical photoreceptors for nonvisual ocular photoreception in mice
2000 StandoutNobel
A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans
2014
Revised diagnostic criteria for the pseudotumor cerebri syndrome in adults and children
2013 Standout
Role of hypoxia and extracellular matrix‐integrin binding in the modulation of angiogenic growth factors secretion by retinal pigmented epithelial cells
1999
Carbonic anhydrase XIV deficiency produces a functional defect in the retinal light response
2007
Splicing in disease: disruption of the splicing code and the decoding machinery
2007
Glial Remodeling and Neural Plasticity in Human Retinal Detachment with Proliferative Vitreoretinopathy
2004
Abnormal Vessel Formation in the Choroid of Mice Lacking Tissue Inhibitor of Metalloprotease-3
2008
Molecular Genetics of Human Retinal Disease
1999
Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies
2004
CSPα-deficiency causes massive and rapid photoreceptor degeneration
2006 StandoutNobel
Molecular composition of drusen as related to substructural phenotype.
1999
Diagnostic criteria for idiopathic intracranial hypertension
2002 Standout
Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3
2003
Allosteric Cascade of Spliceosome Activation
2002
Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change.
1993
How Matrix Metalloproteinases Regulate Cell Behavior
2001 Standout
Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases
2003 Standout
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
2003
Age-Related Macular Degeneration: Review of Pathogenesis
1998
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections
2003
Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice
2002
A Novel Tissue Inhibitor of Metalloproteinases-3 Mutation Reveals a Common Molecular Phenotype in Sorsby's Fundus Dystrophy
2000
Complex expression pattern of RPGR reveals a role for purine-rich exonic splicing enhancers.
2002
Mechanisms of Alternative Pre-Messenger RNA Splicing
2003 Standout
Age-related macular degeneration: review of pathogenesis.
1999
Idiopathic Intracranial Hypertension
1991
Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?
2012 Standout
Works of A.C. Bird being referenced
Helicoidal peripapillary chorioretinal degeneration: electrophysiology and psychophysics in 17 patients
1998
Functional assessment of the native retinal pigment epithelium after the surgical excision of subfoveal choroidal neovascular membranes type II: preliminary results
2001
A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)
2001
Accumulation of tissue inhibitor of metalloproteinases-3 in human eyes with Sorsby's fundus dystrophy or retinitis pigmentosa
1998
Growth of pure cultures of retinal pigment epithelial cells using chorioretinal biopsies from the pig
1988
Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope
1999
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.
1996
Neovaisseaux Sous-Retiniens Maculaires et Laser
1989
An Immunohistochemical Study of an Autosomal Dominant Feline Rod/Cone Dysplasia (Rdy Cats)
1999
Correlation between Biochemical Composition and Fluorescein Binding of Deposits in Bruch's Membrane
1992
Choroidal folds in association with papilloedema.
1973
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus
1999