Exome sequencing reveals CCDC111 mutation associated with high myopia (Q34338729)

1 August 2017

title

Exome sequencing reveals CCDC111 mutation associated with high myopia (English)

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1 August 2017

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Fuxin Zhao

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1 August 2017

Jinyu Wu

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1 August 2017

Anquan Xue

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1 August 2017

Yanfeng Su

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1 August 2017

Xiaojing Wang

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1 August 2017

Xianmin Lu

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1 August 2017

Zhonglou Zhou

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1 August 2017

Jia Qu

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1 August 2017

Xiangtian Zhou

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1 August 2017

publication date

12 April 2013

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1 August 2017

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1 August 2017

volume

132

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1 August 2017

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1 August 2017

page(s)

913-921

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A method and server for predicting damaging missense mutations

1 August 2017

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A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

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A genome-wide scan maps a novel high myopia locus to 5p15.

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A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population

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A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1

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Targeted capture and massively parallel sequencing of 12 human exomes

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Exome sequencing identifies the cause of a mendelian disorder

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Identification of a novel locus on 2q for autosomal dominant high-grade myopia.

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Refractive errors in an elderly Japanese population: the Tajimi study.

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A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population

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Exome sequencing identifies ZNF644 mutations in high myopia

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Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

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Increased prevalence of myopia in the United States between 1971-1972 and 1999-2004.

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TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

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A second locus for familial high myopia maps to chromosome 12q

21 January 2018

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Evidence that a locus for familial high myopia maps to chromosome 18p

21 January 2018

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Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1.

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New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17

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Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family

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12 December 2020

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Prevalence and risk factors for refractive errors in an adult inner city population.

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Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia

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X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.

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A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

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Linkage analysis of high myopia susceptibility locus in 26 families

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12 December 2020

10.1007/S00439-013-1303-6

Identifiers

DOI

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Dimensions Publication ID

1 August 2017

1024283087

0 references

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