Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12 (Q37153179)

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25 January 2020

title

Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12 (English)

1 reference

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25 January 2020

1 reference

1 reference

6

Paul Mitchell

1 reference

18 August 2017

Maria Schäche

1

1 reference

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25 January 2020

Christine Y Chen

2

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25 January 2020

Kelly Kathleen Pertile

3

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25 January 2020

Andrea Jane Richardson

4

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25 January 2020

Mohamed Dirani

5

1 reference

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25 January 2020

Paul Nigel Baird

7

1 reference

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25 January 2020

Paul Mitchell

6

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25 January 2020

publication date

10 April 2009

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25 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19365569 AND SRC:MED&resulttype=core&format=json

25 January 2020

volume

15

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25 January 2020

page(s)

722-730

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19365569 AND SRC:MED&resulttype=core&format=json

Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies

25 January 2020

cites work

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

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Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15.

6 September 2017

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6 September 2017

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Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota

6 September 2017

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6 September 2017

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Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36.

6 September 2017

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Methodology and recruitment of probands and their families for the Genes in Myopia (GEM) Study

6 September 2017

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Heritability of refractive error and familial aggregation of myopia in an elderly American population

6 September 2017

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Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes

6 September 2017

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Prevalence of refractive errors in a rural South Indian population

6 September 2017

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A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins

6 September 2017

1 reference

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Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12

6 September 2017

1 reference

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Problems of reporting genetic associations with complex outcomes

6 September 2017

1 reference

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TGFbeta-induced factor: a candidate gene for high myopia

6 September 2017

1 reference

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Parental myopia, near work, school achievement, and children's refractive error

6 September 2017

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Prevalence rates of refractive errors in Sumatra, Indonesia.

6 September 2017

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A high-resolution recombination map of the human genome

6 September 2017

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The human genome browser at UCSC

6 September 2017

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The importance of genes and environment for ocular refraction and its determiners: a population based study among 20-45 year old twins

6 September 2017

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

6 September 2017

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Prevalence and risk factors of myopia in Victoria, Australia

6 September 2017

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

6 September 2017

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

6 September 2017

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The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

6 September 2017

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Visual impairment in Australia: distance visual acuity, near vision, and visual field findings of the Melbourne Visual Impairment Project

6 September 2017

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

6 September 2017

1 reference

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Referral rates for a functional vision screening among a large cosmopolitan sample of Australian children

6 September 2017

1 reference

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Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.

14 September 2017

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Assessment of TGIF as a candidate gene for myopia

14 September 2017

1 reference

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Refractive error and visual impairment in school children in rural southern China

14 September 2017

1 reference

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Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

Myopia. The nature versus nurture debate goes on.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

The Roles of PAX6 and SOX2 in Myopia: lessons from the 1958 British Birth Cohort.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

Analysis of single nucleotide polymorphisms at 13 loci within the transforming growth factor-induced factor gene shows no association with high myopia in Japanese subjects.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

IQ and the association with myopia in children

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

The SNPs analysis of encoding sequence of interacting factor gene in Chinese population

3 September 2018

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Five-year refractive changes in an older population: the Blue Mountains Eye Study

3 September 2018

1 reference

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A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36.

3 September 2018

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Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis

3 September 2018

1 reference

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The increasing prevalence of myopia: implications for Australia

3 September 2018

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Diabetes, fasting blood glucose and age-related maculopathy: The Blue Mountains Eye Study

3 September 2018

1 reference

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Refractive errors in an older population: the Blue Mountains Eye Study.

3 September 2018

1 reference

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PAX6Mutations May Be Associated with High Myopia

3 September 2018

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Family-Based Association Analysis of Hepatocyte Growth Factor (HGF) Gene Polymorphisms in High Myopia

20 October 2018

1 reference

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Linkage Analysis of the Genetic Loci for High Myopia on 18p, 12q, and 17q in 51 U.K. Families

4 December 2018

1 reference

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Prevalence and risk factors for refractive errors in adult Chinese in Singapore

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2666771

New susceptibility locus for high myopia is linked to the uromodulin-like 1 (UMODL1) gene region on chromosome 21q22.3.

4 December 2018

1 reference

12 December 2020

1 reference

12 December 2020

Genes and environment in refractive error: the twin eye study

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12 December 2020

Refractive errors in a black adult population: the Barbados Eye Study

1 reference

12 December 2020

Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia

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12 December 2020

Genome-wide Scan for Myopia in the Old Order Amish

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12 December 2020

HaploPainter: a tool for drawing pedigrees with complex haplotypes

1 reference

12 December 2020

Blood storage at 4°C—factors involved in DNA yield and quality

1 reference

12 December 2020

Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12

1 reference

12 December 2020

Confirmation of Linkage to Ocular Refraction on Chromosome 22q and Identification of a Novel Linkage Region on 1q

1 reference

12 December 2020

Systematic assessment of the tagging polymorphisms of the COL1A1 gene for high myopia

1 reference

12 December 2020

Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1

1 reference

12 December 2020

Linkage Replication of theMYP12Locus in Common Myopia

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12 December 2020

A PAX6 gene polymorphism is associated with genetic predisposition to extreme myopia

1 reference

12 December 2020

Familial high myopia linkage to chromosome 18p

1 reference

12 December 2020

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

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12 December 2020

Refractive status in the Beaver Dam Eye Study

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19365569 AND SRC:MED&resulttype=core&format=json

25 January 2020

PubMed publication ID

19365569

1 reference