Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness (Q21144980)

16

object named as

Christopher J Hammond

Christopher J

Hammond

1 reference

17 August 2022

5

Kathryn P Burdon

Kathryn P

Burdon

1 reference

17 August 2022

19

David A Mackey

David A

Mackey

1 reference

17 August 2022

14

Nicholas G Martin

Nicholas G

Martin

1 reference

17 August 2022

Yi Lu

1

Yi

Lu

1 reference

17 August 2022

Stuart Macgregor

17

Stuart

Macgregor

1 reference

17 August 2022

Grant W Montgomery

11

Grant W

Montgomery

1 reference

17 August 2022

9

Paul Mitchell

Paul

Mitchell

1 reference

17 August 2022

4

Alex W Hewitt

Alex W

Hewitt

1 reference

17 August 2022

13

Timothy D Spector

Timothy D

Spector

1 reference

17 August 2022

18

Jamie E

Craig

Jamie E Craig

1 reference

17 August 2022

David P Dimasi

2

David P

Dimasi

1 reference

17 August 2022

Pirro G Hysi

3

Pirro G

Hysi

1 reference

17 August 2022

Tze'Yo Toh

6

Tze'Yo

Toh

1 reference

17 August 2022

Jonathan B Ruddle

7

Jonathan B

Ruddle

1 reference

17 August 2022

Yi Ju Li

8

Yi Ju

Li

1 reference

17 August 2022

Paul R Healey

10

Paul R

Healey

1 reference

17 August 2022

Terri L Young

15

Terri L

Creative Commons Attribution 4.0 International

Young

1 reference

17 August 2022

language of work or name

English

0 references

publication date

May 2010

0 references

published in

PLOS Genetics

0 references

volume

6

0 references

issue

5

0 references

page(s)

e1000947

0 references

copyright license

start time

13 May 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

The number of people with glaucoma worldwide in 2010 and 2020

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Structural abnormalities of the cornea and lid resulting from collagen V mutations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Principal components analysis corrects for stratification in genome-wide association studies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Benign joint hypermobility syndrome: evaluation, diagnosis, and management

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Rapid inexpensive genome-wide association using pooled whole blood

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

The genetics of central corneal thickness

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Geographical structure and differential natural selection among North European populations

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Common sequence variants on 20q11.22 confer melanoma susceptibility

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Predictors of long-term progression in the early manifest glaucoma trial

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Efficient association mapping of quantitative trait loci with selective genotyping

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

Intercurrent factors associated with the development of open-angle glaucoma in the European glaucoma prevention study

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

The Ocular Hypertension Treatment Study: baseline factors that predict the onset of primary open-angle glaucoma.

27 September 2017

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Markedly increased central corneal thickness: an unrecognized finding in congenital aniridia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Analysis of myocilin mutations in 1703 glaucoma patients from five different populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Genetic covariation of pelvic organ and elbow mobility in twins and their sisters

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Distribution of central corneal thickness and its association with intraocular pressure: The Rotterdam Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Optimal selection strategies for QTL mapping using pooled DNA samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000947

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2869325

The heritability of optic disc parameters: a classic twin study

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20485516

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cornea in Marfan disease: Orbscan and in vivo confocal microscopy analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20485516

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Central corneal thickness in osteogenesis imperfecta and otosclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20485516

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1000947

1 reference

4367490

4367490

1 reference

1 reference

1 reference