EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa
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Title
EYS
mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa
Authors
Keywords
-
Journal
HUMAN MUTATION
Volume 39, Issue 2, Pages 177-186
Publisher
Wiley
Online
2017-11-21
DOI
10.1002/humu.23371
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Note: Only part of the references are listed.- Diagnostic exome sequencing in 266 Dutch patients with visual impairment
- (2017) Lonneke Haer-Wigman et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy
- (2017) Zhaojing Lu et al. Scientific Reports
- CRISPR/Cas9 in zebrafish: an efficient combination for human genetic diseases modeling
- (2016) Jiaqi Liu et al. HUMAN GENETICS
- Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease
- (2016) Riccardo Sangermano et al. OPHTHALMOLOGY
- Eyes shut homolog is required for maintaining the ciliary pocket and survival of photoreceptors in zebrafish
- (2016) Miao Yu et al. Biology Open
- Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population
- (2016) Yanan Di et al. Scientific Reports
- Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa
- (2016) Raquel Perez-Carro et al. Scientific Reports
- Identifying mutations in Tunisian families with retinal dystrophy
- (2016) Imen Habibi et al. Scientific Reports
- The diagnostic application of targeted re-sequencing in Korean patients with retinitis pigmentosa
- (2015) Chang-Ki Yoon et al. BMC GENOMICS
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies
- (2015) Ralph W.N. Slijkerman et al. PROGRESS IN RETINAL AND EYE RESEARCH
- NGS-based Molecular diagnosis of 105 eyeGENE® probands with Retinitis Pigmentosa
- (2015) Zhongqi Ge et al. Scientific Reports
- Targeted Next-generation Sequencing Reveals Novel EYS Mutations in Chinese Families with Autosomal Recessive Retinitis Pigmentosa
- (2015) Xue Chen et al. Scientific Reports
- Retinitis Pigmentosa withEYSMutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations
- (2015) Yuuki Arai et al. Journal of Ophthalmology
- Autosomal recessive cone–rod dystrophy associated with compound heterozygous mutations in the EYS gene
- (2014) Satoshi Katagiri et al. DOCUMENTA OPHTHALMOLOGICA
- Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations
- (2014) C.O. Pierrottet et al. GENETICS AND MOLECULAR RESEARCH
- Genotype–phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing
- (2014) Xiu-Feng Huang et al. GENETICS IN MEDICINE
- Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible and more sensitive for variant detection, than exome sequencing
- (2014) Mark B. Consugar et al. GENETICS IN MEDICINE
- Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations
- (2014) Vera L. Bonilha et al. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
- Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing
- (2014) Yan Xu et al. HUMAN GENETICS
- CRISPR-Cas systems for editing, regulating and targeting genomes
- (2014) Jeffry D Sander et al. NATURE BIOTECHNOLOGY
- A general framework for estimating the relative pathogenicity of human genetic variants
- (2014) Martin Kircher et al. NATURE GENETICS
- Stem Cells as Tools for Studying the Genetics of Inherited Retinal Degenerations
- (2014) L. A. Wiley et al. Cold Spring Harbor Perspectives in Medicine
- Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies
- (2013) Nicola Glöckle et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in theEYSGene
- (2013) Kimiko Suto et al. OPHTHALMIC GENETICS
- Increasing the Yield in Targeted Next-Generation Sequencing by Implicating CNV Analysis, Non-Coding Exons and the Overall Variant Load: The Example of Retinal Dystrophies
- (2013) Tobias Eisenberger et al. PLoS One
- Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
- (2013) K. M. Nishiguchi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes
- (2012) L. Abu-Safieh et al. GENOME RESEARCH
- Next-generation genetic testing for retinitis pigmentosa
- (2012) Kornelia Neveling et al. HUMAN MUTATION
- A paradigm shift in the delivery of services for diagnosis of inherited retinal disease
- (2012) James O'Sullivan et al. JOURNAL OF MEDICAL GENETICS
- Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases
- (2012) Isabelle Audo et al. Orphanet Journal of Rare Diseases
- Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population
- (2012) Katsuhiro Hosono et al. PLoS One
- Mutation Screening of Multiple Genes in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing
- (2011) María González-del Pozo et al. PLoS One
- Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa
- (2010) Yukan Huang et al. BMC Medical Genetics
- EYS is a major gene for rod-cone dystrophies in France
- (2010) Isabelle Audo et al. HUMAN MUTATION
- Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa
- (2010) Isabel Barragán et al. HUMAN MUTATION
- Mutations in the EYS Gene Account for Approximately 5% of Autosomal Recessive Retinitis Pigmentosa and Cause a Fairly Homogeneous Phenotype
- (2010) Karin W. Littink et al. OPHTHALMOLOGY
- Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa
- (2008) Rob W.J. Collin et al. AMERICAN JOURNAL OF HUMAN GENETICS
- EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
- (2008) Mai M Abd El-Aziz et al. NATURE GENETICS
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