(Q28751780)

13

Nagahisa Yoshimura

0 references

Keitaro Matsuo

11

Keitaro Matsuo

0 references

Kazuo Tajima

12

Kazuo Tajima

0 references

Hideo Nakanishi

1

Hideo Nakanishi

0 references

Norimoto Gotoh

3

Norimoto Gotoh

0 references

Hisako Hayashi

4

Hisako Hayashi

0 references

Kenji Yamashiro

5

Kenji Yamashiro

0 references

Masaaki Saito

9

Masaaki Saito

0 references

Tomohiro Iida

10

Tomohiro Iida

0 references

Fumihiko Matsuda

14

Fumihiko Matsuda

0 references

author name string

Ryo Yamada

2

0 references

Noriaki Shimada

6

0 references

Manabu Mochizuki

Creative Commons Attribution 4.0 International

8

0 references

language of work or name

English

0 references

publication date

September 2009

0 references

published in

PLOS Genetics

0 references

volume

5

0 references

issue

9

0 references

page(s)

e1000660

0 references

copyright license

start time

25 September 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

HTRA1 promoter polymorphism in wet age-related macular degeneration

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Complement factor H polymorphism in age-related macular degeneration

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Complement factor H variant increases the risk of age-related macular degeneration

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Haploview: analysis and visualization of LD and haplotype maps

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Genomic control for association studies

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

The future of genetic studies of complex human diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Complement factor H polymorphism and age-related macular degeneration

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

An international collaborative family-based whole-genome linkage scan for high-grade myopia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Linkage analysis of high myopia susceptibility locus in 26 families

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

A review of current approaches to identifying human genes involved in myopia.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Power to detect risk alleles using genome-wide tag SNP panels

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Complex trait genetics of refractive error

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Heritability of refractive error and ocular biometrics: the Genes in Myopia (GEM) twin study.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Causes of blindness and visual impairment in urban and rural areas in Beijing: the Beijing Eye Study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

A genetic perspective on myopia.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

The prevalence of refractive errors among adults in the United States, Western Europe, and Australia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

BRCC2, a novel BH3-like domain-containing protein, induces apoptosis in a caspase-dependent manner

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

On estimating the relation between blood group and disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

JSNP: a database of common gene variations in the Japanese population

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Apoptosis in human retinal degenerations.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Mantel-Haenszel statistics and direct standardization.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Axial length measurements and fundus changes of the myopic eye. I. The posterior fundus

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

3 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

Refractive error, ocular biometry, and lens opalescence in an adult population: the Los Angeles Latino Eye Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults: the Copenhagen City Eye Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

Variations in ocular biometry in an adult Chinese population in Singapore: the Tanjong Pagar Survey

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735651

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

27 November 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000660

Basic fibroblast growth factor suppresses retinal neuronal apoptosis in form-deprivation myopia in chicks

21 January 2018

1 reference

12 December 2020

Heritability of refractive value and ocular biometrics

1 reference

12 December 2020

Age-Specific Prevalence and Causes of Blindness and Visual Impairment in an Older Population

1 reference

12 December 2020

No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese

1 reference

12 December 2020

Genes and environment in refractive error: the twin eye study

1 reference

12 December 2020

Prevalence and causes of low vision and blindness in a Japanese adult population: the Tajimi Study

1 reference

12 December 2020

Support for Polygenic Influences on Ocular Refractive Error

1 reference

12 December 2020

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

1 reference

12 December 2020