New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. (Q34131948)

31 July 2017

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. (English)

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31 July 2017

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Igor Rudan

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Veronique Vitart

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Veronique Vitart

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Lina Zgaga

11

Lina Zgaga

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James F. Wilson

James F Wilson

16

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Pau Navarro

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Pau Navarro

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31 July 2017

18

Harry Campbell

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31 July 2017

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Jennifer Huffman

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31 July 2017

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Nicholas D Hastie

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31 July 2017

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Grgo Gunjaca

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31 July 2017

12

Ivana Kolcić

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31 July 2017

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Zoran Vatavuk

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31 July 2017

2

Goran Bencić

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31 July 2017

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Jelena Skunca Herman

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31 July 2017

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Kajo Bućan

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31 July 2017

Susan Campbell

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31 July 2017

Josipa Marin

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31 July 2017

Mirna Kirin

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31 July 2017

Brian Fleck

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31 July 2017

Alan Wright

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31 July 2017

18 August 2010

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31 July 2017

Human Molecular Genetics

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31 July 2017

19

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31 July 2017

4304-4311

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31 July 2017

21

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Corneal and scleral collagens--a microscopist's perspective

31 July 2017

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Corneal thickness measurement in the management of primary open-angle glaucoma: a report by the American Academy of Ophthalmology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Orbscan mapping in Ehlers-Danlos syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Heritability of central corneal thickness in Chinese: the Guangzhou Twin Eye Study

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Heritabilities of ocular biometrical traits in two croatian isolates with extended pedigrees

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Central corneal thickness is highly heritable: the twin eye studies.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Development of the corneal stroma, and the collagen-proteoglycan associations that help define its structure and function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Genetic comparison of a Croatian isolate and CEPH European founders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Collagen type I and type V are present in the same fibril in the avian corneal stroma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Another look at collagen V and XI molecules.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Type V collagen: heterotypic type I/V collagen interactions in the regulation of fibril assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Interpretation of association signals and identification of causal variants from genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Foxf1 and Foxf2 control murine gut development by limiting mesenchymal Wnt signaling and promoting extracellular matrix production

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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/10.1093%2FHMG%2FDDQ349

Rare variants create synthetic genome-wide associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Ocular forkhead transcription factors: seeing eye to eye.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

The phenotype of limbal epithelial stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Genome-wide association study identifies five loci associated with lung function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

GenABEL: an R library for genome-wide association analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

ProbABEL package for genome-wide association analysis of imputed data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Pedigree analysis for quantitative traits: variance components without matrix inversion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Family-based association tests for genomewide association scans

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ349

21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ349

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31 July 2017

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