Prioritization of Retinal Disease Genes: An Integrative Approach-Reference-Cited by-同舟云学术

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Prioritization of Retinal Disease Genes: An Integrative Approach

Published:2013-04-12 Issue:6 Volume:34 Page:853-859
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Wagner Alex H.,Taylor Kyle R.¹,DeLuca Adam P.²,Casavant Thomas L.,Mullins Robert F.³,Stone Edwin M.³,Scheetz Todd E.,Braun Terry A.

Affiliation:

1. Department of Electrical and Computer Engineering; University of Iowa; Iowa City; Iowa

2. Department of Biomedical Engineering; University of Iowa; Iowa City; Iowa

3. Department of Ophthalmology and Visual Sciences; University of Iowa; Iowa City; Iowa

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22317/fullpdf

Reference57 articles.

1. A map of human genome variation from population-scale sequencing;Durbin;Nature,2010

2. Gene prioritization through genomic data fusion;Aerts;Nat Biotechnol,2006

3. Predicting candidate genes for human deafness disorders: a bioinformatics approach;Alsaber;BMC Genomics,2006

4. Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2;Badano;Am J Hum Genet,2003

5. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3;Banerjee;Genomics,1998

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Survey of Gene Prioritization Tools for Mendelian and Complex Human Diseases;Journal of Integrative Bioinformatics;2019-09-09

2. Analysis of Computational Gene Prioritization Approaches;Procedia Computer Science;2018

3. Retinal expression and localization of Mef2c support its important role in photoreceptor gene expression;Biochemical and Biophysical Research Communications;2017-01

4. Hypomorphic mutations inTRNT1cause retinitis pigmentosa with erythrocytic microcytosis;Human Molecular Genetics;2015-10-22

5. Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy;Genetics in Medicine;2014-09

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