Citation Impact
Citing Papers
Transposition-Driven Genomic Heterogeneity in the Drosophila Brain
2013 StandoutScienceNobel
Developmental refinement of hair cell synapses tightens the coupling of Ca 2 + influx to exocytosis
2014 StandoutNobel
Biological Functions of the Small Leucine-rich Proteoglycans: From Genetics to Signal Transduction
2008
RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport Proteins
2005
A Visualizable Chain‐Terminating Inhibitor of Glycosaminoglycan Biosynthesis in Developing Zebrafish
2014 StandoutNobel
Merkel Cells Activate Sensory Neural Pathways through Adrenergic Synapses
2018 StandoutNobel
LINEs, SINEs and processed pseudogenes: parasitic strategies for genome modeling
2005
Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
2011
Myopia
2012 Standout
TSPAN12 Regulates Retinal Vascular Development by Promoting Norrin- but Not Wnt-Induced FZD4/β-Catenin Signaling
2009
Mechanisms and Functional Implications of Adult Neurogenesis
2008 Standout
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
2009 StandoutNobel
The Blood–Brain Barrier
2015 Standout
A Novel Locus (RP24) for X-linked Retinitis Pigmentosa Maps to Xq26-27
1998
The leucine-rich repeat structure
2008
Differentiation of the brain vasculature: the answer came blowing by the Wnt
2010
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Gabapentin Receptor α2δ-1 Is a Neuronal Thrombospondin Receptor Responsible for Excitatory CNS Synaptogenesis
2009
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy
2010
Norrin/Frizzled4 Signaling in Retinal Vascular Development and Blood Brain Barrier Plasticity
2012
Secreted and Transmembrane Wnt Inhibitors and Activators
2012
Outdoor Activity Reduces the Prevalence of Myopia in Children
2008 Standout
Alternative RNA splicing in the nervous system
2001
The Science of Stroke: Mechanisms in Search of Treatments
2010 Standout
An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex
2014 Standout
Molecular basis of ancestral vertebrate electroreception
2017 StandoutNatureNobel
Proteoglycan form and function: A comprehensive nomenclature of proteoglycans
2015
Mutational Analysis of Norrin-Frizzled4 Recognition
2006
Vascular morphogenesis: a Wnt for every vessel?
2009
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
Ganglion-specific splicing of TRPV1 underlies infrared sensation in vampire bats
2011 StandoutNatureNobel
RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa
2003
Metazoan MicroRNAs
2018 Standout
Next generation tools for the annotation of human SNPs
2009
Extracellular matrix structure
2015 Standout
The Molecular Architecture of Ribbon Presynaptic Terminals
2009
LINE-1 retrotransposons: Modulators of quantity and quality of mammalian gene expression?
2005
Development of the retinal vasculature
2007
dbRIP: A highly integrated database of retrotransposon insertion polymorphisms in humans
2006
Wnt/β-Catenin Signaling and Disease
2012 Standout
Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
2005 Nature
Retinitis pigmentosa
2006 Standout
Development, maintenance and disruption of the blood-brain barrier
2013 Standout
The Ca2+Channel Subunit β2 Regulates Ca2+Channel Abundance and Function in Inner Hair Cells and Is Required for Hearing
2009
Remodelling the extracellular matrix in development and disease
2014 Standout
Genomic Analysis of Reactive Astrogliosis
2012 Standout
ABySS: A parallel assembler for short read sequence data
2009 Standout
The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease
2010
Mice deficient in small leucine-rich proteoglycans: novel in vivo models for osteoporosis, osteoarthritis, Ehlers-Danlos syndrome, muscular dystrophy, and corneal diseases
2002
The Association between Time Spent Outdoors and Myopia in Children and Adolescents
2012 Standout
Leucine-Rich Repeat Transmembrane Proteins Are Essential for Maintenance of Long-Term Potentiation
2013 StandoutNobel
A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system☆☆Sequence data from this article have been deposited with the DDBJ/EMBL/GenBank Data Libraries under Accession Nos. AY182024 (human LRRTM1), AY182026 (human LRRTM2), AY182028 (human LRRTM3), AY182030 (human LRRTM4), AY182025 (mouse LRRTM1), AY182027 (mouse LRRTM2), AY182029 (mouse LRRTM3), and AY182031 (mouse LRRTM4).
2003
Extracellular Matrix Molecules: Potential Targets in Pharmacotherapy
2009
ECAT11/L1td1 Is Enriched in ESCs and Rapidly Activated During iPSCGeneration, but It Is Dispensable for the Maintenance and Induction of Pluripotency
2011 StandoutNobel
Basic and Therapeutic Aspects of Angiogenesis
2011 Standout
Reactive Astrocytes: Production, Function, and Therapeutic Potential
2017 Standout
Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization
2009
The epidemiology of retinitis pigmentosa in Denmark
2002
A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa
2004
Mobile elements and the human genome
2000
Probing the Functional Equivalence of Otoferlin and Synaptotagmin 1 in Exocytosis
2011 StandoutNobel
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
2010 Standout
How genetic is school myopia?
2004
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
2017 Standout
The ORF1 Protein Encoded by LINE‐1: Structure and Function During L1 Retrotransposition
2006
Homeostasis of Eye Growth and the Question of Myopia
2004 Standout
Multi-functional norrin is a ligand for the LGR4 receptor
2013 Standout
LRG1 promotes angiogenesis by modulating endothelial TGF-β signalling
2013 StandoutNature
A unified classification system for eukaryotic transposable elements
2007 Standout
Glycosaminoglycans and their proteoglycans: host‐associated molecular patterns for initiation and modulation of inflammation
2006 Standout
The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo
2011 StandoutNobel
Inactivation of the microRNA-183/96/182cluster results in syndromic retinal degeneration
2013
Molecular Mechanisms of Metabolic Resistance to Synthetic and Natural Xenobiotics
2006 Standout
The Molecular Diversity of Glycosaminoglycans Shapes Animal Development
2006
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
2005 Standout
VEGF Secreted by Hypoxic Müller Cells Induces MMP-2 Expression and Activity in Endothelial Cells to Promote Retinal Neovascularization in Proliferative Diabetic Retinopathy
2013 StandoutNobel
The extracellular matrix at a glance
2010 Standout
A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors
2009 Standout
The structural basis of lipopolysaccharide recognition by the TLR4–MD-2 complex
2009 StandoutNature
Functional redundancy of cryptochromes and classical photoreceptors for nonvisual ocular photoreception in mice
2000 StandoutNobel
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting
2003
Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
2000
RPGR Isoforms in Photoreceptor Connecting Cilia and the Transitional Zone of Motile Cilia
2003
The Inflammasomes: Guardians of the Body
2009 Standout
Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons
2011 StandoutNobel
Molecular Genetics of Human Retinal Disease
1999
LRR-containing receptors regulating plant development and defense
2003
The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease
2017
Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3
2003
COMPARATIVE PRIMATE GENOMICS
2004 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Wnt Signaling Mediates Pathological Vascular Growth in Proliferative Retinopathy
2011
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
2003
Mechanisms of Alternative Pre-Messenger RNA Splicing
2003 Standout
X-linked Retinitis Pigmentosa:RPGRMutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15
2003
Works of Silke Feil being referenced
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
2000
Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy
2006
Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)
1999
RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa
1999
Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled‐4
2008
Overexpression of RPGR Leads to Male Infertility in Mice Due to Defects in Flagellar Assembly1
2008
Positional cloning of the gene for X-linked retinitis pigmentosa 2
1998
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking
2007
Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature
2005
NYX(Nyctalopin on Chromosome X), the Gene Mutated in Congenital Stationary Night Blindness, Encodes a Cell Surface Protein
2003
Structural and Functional Abnormalities of Retinal Ribbon Synapses due toCacna2d4Mutation
2006
Differential Gene Expression inNdph-Knockout Mice in Retinal Development
2009
Cone versus Rod Disease in a MutantRpgrMouse Caused by Different Genetic Backgrounds
2010