‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration
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Qi Liu | Fan Lu | Jia Qu | Jinyu Wu | Xia Ran | Wei-Jun Cai | Xiu-Feng Huang | Zi-Bing Jin | Qi Liu | Jinyu Wu | F. Lu | J. Qu | W. Cai | Xia Ran | Xiu-Feng Huang | Zi‐Bing Jin
[1] John Broxholme,et al. Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease , 2012, European Journal of Human Genetics.
[2] Carsten Bergmann,et al. Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3 , 2012, Orphanet Journal of Rare Diseases.
[3] Peter Devilee,et al. Leiden open variation database of the MUTYH gene , 2010, Human mutation.
[4] Jing Wang,et al. WEB-based GEne SeT AnaLysis Toolkit (WebGestalt): update 2013 , 2013, Nucleic Acids Res..
[5] K. Kaczyńska,et al. Long-term neuroprotective effects of NT-4-engineered mesenchymal stem cells injected intravitreally in a mouse model of acute retinal injury. , 2013, Investigative ophthalmology & visual science.
[6] Fowzan S Alkuraya,et al. Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes , 2013, Genome research.
[7] Makoto Nakamura,et al. Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene , 2013, Proceedings of the National Academy of Sciences.
[8] Xavier Zanlonghi,et al. Mutations in IMPG1 cause vitelliform macular dystrophies. , 2013, American journal of human genetics.
[9] John G. Flannery,et al. Transgenic Animal Models for the Study of Inherited Retinal Dystrophies. , 1999, ILAR journal.
[10] J. Zenteno,et al. Exome sequencing identifies RDH12 compound heterozygous mutations in a family with severe retinitis pigmentosa. , 2013, Gene.
[11] Alan F. Scott,et al. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders , 2002, Nucleic Acids Res..
[12] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[13] Christian Gilissen,et al. Next-generation genetic testing for retinitis pigmentosa , 2012, Human mutation.
[14] S. Daiger,et al. Genes and mutations causing retinitis pigmentosa , 2013, Clinical genetics.
[15] Mary Goldman,et al. The UCSC Genome Browser database: update 2011 , 2010, Nucleic Acids Res..
[16] John Broxholme,et al. Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease , 2013, European Journal of Human Genetics.
[17] Shinsei Minoshima,et al. Keio Mutation Database for eye disease genes (KMeyeDB) , 1999, Nucleic Acids Res..
[18] Martha L Zettel,et al. Effects of aging and sensory loss on glial cells in mouse visual and auditory cortices , 2012, Glia.
[19] David Haussler,et al. The UCSC genome browser database: update 2007 , 2006, Nucleic Acids Res..
[20] S Minoshima,et al. Eye disorder database “KMeyeDB” , 2000, Human mutation.
[21] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[22] Madeline A Lancaster,et al. The primary cilium as a cellular signaling center: lessons from disease. , 2009, Current opinion in genetics & development.
[23] Kenny Q. Ye,et al. An integrated map of genetic variation from 1,092 human genomes , 2012, Nature.
[24] T. Webb,et al. Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23). , 2012, Human molecular genetics.
[25] Val C. Sheffield,et al. BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking , 2013, Journal of Cell Science.
[26] S. Daiger,et al. Identifying retinal disease genes: how far have we come, how far do we have to go? , 2004, Novartis Foundation symposium.
[27] Caroline C W Klaver,et al. Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy. , 2013, American journal of human genetics.
[28] Wah Chiu,et al. Three-Dimensional Architecture of the Rod Sensory Cilium and Its Disruption in Retinal Neurodegeneration , 2012, Cell.
[29] Cheryl M Craft,et al. Potential cellular functions of N-ethylmaleimide sensitive factor in the photoreceptor. , 2012, Advances in experimental medicine and biology.
[30] Bing Zhang,et al. WebGestalt: an integrated system for exploring gene sets in various biological contexts , 2005, Nucleic Acids Res..
[31] E. Zrenner,et al. Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies , 2013, European Journal of Human Genetics.
[32] S. Jacobson,et al. Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing , 2013, Journal of Medical Genetics.
[33] José Martín-Nieto,et al. Alterations in Energy Metabolism, Neuroprotection and Visual Signal Transduction in the Retina of Parkinsonian, MPTP-Treated Monkeys , 2013, PloS one.
[34] Shinsei Minoshima,et al. KMeyeDB: a graphical database of mutations in genes that cause eye diseases , 2010, Human mutation.