(Q36967234)

17 August 2017

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

1 reference

17 August 2017

1 reference

1 reference

whole genome sequencing

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11

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17 August 2017

2

Jeremy A Guggenheim

1 reference

17 August 2017

Yi-Ju Li

1

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David A. Mackey

object named as

David A Mackey

15

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author name string

Anuradha Bulusu

3

1 reference

17 August 2017

Ravikanth Metlapally

4

1 reference

17 August 2017

Diana Abbott

5

1 reference

17 August 2017

Francois Malecaze

6

1 reference

17 August 2017

Patrick Calvas

7

1 reference

17 August 2017

Thomas Rosenberg

8

1 reference

17 August 2017

Sandrine Paget

9

1 reference

17 August 2017

Rosalind C Creer

10

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17 August 2017

Michael J Owen

12

1 reference

17 August 2017

Bei Zhao

13

1 reference

17 August 2017

Tristan White

14

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17 August 2017

Terri L Young

16

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17 August 2017

language of work or name

English

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publication date

25 March 2009

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Investigative Ophthalmology Visual Science

17 August 2017

1 reference

17 August 2017

50

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17 August 2017

7

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17 August 2017

3116-3127

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

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Family studies on ocular refraction and its components

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Refractive errors in medical students in Singapore.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Improved inference of relationship for pairs of individuals

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Statistical tests for detection of misspecified relationships by use of genome-screen data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Prevalence and risk factors of myopia in Victoria, Australia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Terminal syringohydromyelia and occult spinal dysraphism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Common causes of blindness and visual handicap in the west of Scotland.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Selected review on genetic factors in myopia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Accurate inference of relationships in sib-pair linkage studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Exact tests for association between alleles at arbitrary numbers of loci

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Progression of myopia in youth: age of cessation.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

On the etiology of myopia. An epidemiological study

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Segregation analysis of ocular refraction and myopia

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Impact of heredity in myopia

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

X-linked cone dysfunction syndrome with myopia and protanopia

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Family aggregation of high myopia: estimation of the sibling recurrence risk ratio.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

X-linked high myopia associated with cone dysfunction.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

Genetic loci for pathological myopia are not associated with juvenile myopia

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

The heritability of high myopia: a reanalysis of Goldschmidt's data

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696634

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

4 December 2018

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

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

1 reference

12 December 2020

Genes and environment in refractive error: the twin eye study

1 reference

12 December 2020

A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on 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

1 reference

12 December 2020

Prevalence of myopia in local and international schools in Hong Kong

1 reference

12 December 2020

Study of myopia among aboriginal school children in Taiwan

1 reference

12 December 2020

VISION 2020-the right to sight: from strategies to action

1 reference

12 December 2020

Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity

1 reference

12 December 2020

Support for Polygenic Influences on Ocular Refractive Error

1 reference

12 December 2020

Genome-wide Scan for Myopia in the Old Order Amish

1 reference

12 December 2020

Identifiers

DOI

10.1167/IOVS.08-2781

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

19324860

1 reference