Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families-Reference-Cited by-同舟云学术

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families

Published:2019-01-31 Issue:1 Volume:20 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Simpson Claire L.,Musolf Anthony M.,Li Qing,Portas Laura,Murgia Federico,Cordero Roberto Y.,Cordero Jennifer B.,Moiz Bilal A.,Holzinger Emily R.,Middlebrooks Candace D.,Lewis Deyana D.,Bailey-Wilson Joan E.^ORCID,Stambolian Dwight

Funder

National Eye Institute

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-019-0752-8.pdf

Reference66 articles.

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2. Wojciechowski R, Hysi PG. Focusing in on the complex genetics of myopia. PLoS Genet. 2013;9(4):e1003442.

3. Simpson CL, Wojciechowski R, Oexle K, Murgia F, Portas L, Li X, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. PLoS One. 2014;9(9):e107110.

4. Solouki AM, Verhoeven VJ, van Duijn CM, Verkerk AJ, Ikram MK, Hysi PG, et al. A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Nat Genet. 2010;42(10):897–901.

5. Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum Mol Genet. 2013;22(13):2754–64.

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