(Q34131948)

31 July 2017

title

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

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31 July 2017

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31 July 2017

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31 July 2017

Igor Rudan

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Veronique Vitart

object named as

Veronique Vitart

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Lina Zgaga

object named as

Lina Zgaga

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James F Wilson

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Pau Navarro

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31 July 2017

Harry Campbell

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31 July 2017

Jennifer Huffman

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31 July 2017

Nicholas D Hastie

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31 July 2017

Grgo Gunjaca

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31 July 2017

Ivana Kolcić

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31 July 2017

Zoran Vatavuk

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31 July 2017

Goran Bencić

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31 July 2017

Jelena Skunca Herman

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31 July 2017

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

publication date

18 August 2010

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31 July 2017

published in

Human Molecular Genetics

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

4304-4311

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Corneal and scleral collagens--a microscopist's perspective

31 July 2017

cites work

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

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

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

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

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Another look at collagen V and XI molecules.

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

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

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

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

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

21 January 2018

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

21 January 2018

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Rare variants create synthetic genome-wide associations

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Ocular forkhead transcription factors: seeing eye to eye.

21 January 2018

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

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The phenotype of limbal epithelial stem cells

21 January 2018

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

21 January 2018

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

21 January 2018

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GenABEL: an R library for genome-wide association analysis

21 January 2018

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ProbABEL package for genome-wide association analysis of imputed data

21 January 2018

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Pedigree analysis for quantitative traits: variance components without matrix inversion

21 January 2018

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Family-based association tests for genomewide association scans

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ349

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31 July 2017

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