About: Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

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About: Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus Goto Sponge NotDistinct Permalink

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scientific article published on 06 January 2013

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2013 (ast) наукова стаття, опублікована в січні 2013 (uk) scientific article published on 06 January 2013 (en) مقالة علمية نشرت في 06 يناير 2013 (ar)
publication date	wds:Q37037658-33C02DC9-F06B-40CA-9A60-6BF03F337BD6
publication date	2013-01-06 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37037658-5D541EBE-CBC9-4950-9F6C-1B44B7AA26FB
language of work or name	English
exact match	wds:Q37037658-9A61B4DE-12A7-4D87-811D-59001A7A66DA
exact match	https://scigraph.springernature.com/pub.10.1038/ng.2506
cites work	wds:Q37037658-04E6D472-4789-4687-946F-7704EF55B137 wds:Q37037658-06E48272-1684-431B-AA6C-C9FBF6C73F80 wds:Q37037658-095EDD49-BDCB-4B3C-8DD8-1DCE9DB54567 wds:Q37037658-0C3F7AB5-07CE-4C97-BC30-52A4B427FD54 wds:Q37037658-0D4B112B-59A1-4057-922F-7ADBFAEA5664 wds:Q37037658-0E49768C-F4A6-4E46-8ADB-8CBFD70152A7 wds:Q37037658-0EA56182-ED7F-4B1B-8172-5157635AA977 wds:Q37037658-11F5CE98-D68E-4B9A-A375-1703CBAF2A00 wds:Q37037658-18F75F42-F8DE-43DA-B7F8-0DA24DF6D292 wds:Q37037658-22E5554C-9938-4719-8F1D-04D58E26E46E wds:Q37037658-2659F66E-C645-4909-9BC3-FFBE49C88D7E wds:Q37037658-28904559-5F15-41F2-917E-8FE16F374200 wds:Q37037658-2A22759C-6D90-4BEA-957A-414CE86BFB9F wds:Q37037658-32D906A6-82F5-449C-8A5A-673D2E9D47AE wds:Q37037658-3606647B-E43E-4214-BF42-E0CA4540F8A2 wds:Q37037658-39B415EC-57D8-4362-832F-012BF291983E wds:Q37037658-39F9DFF0-E85C-4CA5-AC80-32FAC0C7D0BA wds:Q37037658-3AE585AF-C05F-45C6-857D-E97BACC132BE wds:Q37037658-461CFDC0-3EB7-477D-812C-C0F082CE7023 wds:Q37037658-4CD4EE0B-C909-4C20-99D7-96F12755D7C9 wds:Q37037658-4F7B33B7-8143-46C2-A629-DBB2CA7DC67E wds:Q37037658-50670859-662D-4403-97CB-C7A93050B247 wds:Q37037658-569629F5-7D62-4963-87B4-333AFE9BB7AA wds:Q37037658-588B8F01-3DE5-48CF-8B64-016CC0243A20 wds:Q37037658-6C866693-FE3C-414B-946A-8780AEBB83B2 wds:Q37037658-760FAF3D-D620-427F-B59B-71827690BE2E wds:Q37037658-77534B06-DFAC-4D77-99B4-1319266E784F wds:Q37037658-77FC7F30-A196-4D33-97B8-95A2B133295C wds:Q37037658-7A9CC831-EB44-4DBA-A1CF-9C3C9B45BFCB wds:Q37037658-7C4C6BB3-AFCC-4F03-B194-F2E047905006 wds:Q37037658-82024F3A-5149-4EDC-B162-1BD20E1BADB2 wds:Q37037658-87C25F70-A9A8-481C-A1D5-9A85B4ED5398 wds:Q37037658-8B9FD3D5-2A41-4524-9864-418CE689E492 wds:Q37037658-8C88760B-14AE-47DD-ADAC-8E09A795AD6D wds:Q37037658-8F7BAEA0-86A5-4AC1-9F0D-55D8BB3CC1EE wds:Q37037658-958F5324-4CCB-4DCA-A890-EEE67E55E69B wds:Q37037658-9B7D7BA2-72ED-424C-82D7-C5665DA15963 wds:Q37037658-AB8EFE7D-BB20-4FF8-A524-03A533C2C5FD wds:Q37037658-AC61F3BB-E6D7-461B-BE5E-9112F1302AA2 wds:Q37037658-B822C236-C92D-42B3-BE70-2504A1E2AA28 wds:Q37037658-C15DDC6B-7225-46C6-A1AC-F0A0F05194CB wds:Q37037658-CC60A178-C183-4E5D-9AD8-5D4D862B1DB3 wds:Q37037658-CDE5037A-3FE6-48BA-8DA4-E97D30A6E58B wds:Q37037658-CDF8BFFD-2A8A-4BFD-B135-ABB85A27A736 wds:Q37037658-D312491A-E783-4828-BA87-47CEC99A60FA wds:Q37037658-D7319DD6-8C01-4681-969A-E5E690FBDC9C wds:Q37037658-D829346A-0815-4A73-B3AA-3E8AE305FCA8 wds:Q37037658-D8C04C33-49F5-4B16-B393-8C6C0D7B8985 wds:Q37037658-DE5012E5-1439-4EA4-91B3-880CAD0216DC wds:Q37037658-E5E2E8AE-FFF8-40D6-AEFB-46826C0E0E08 wds:Q37037658-ED3C43BD-47D6-41A8-977B-B361816ABA83 wds:Q37037658-EE43E6DD-1B16-41B5-96FC-C24F9552616C wds:Q37037658-F2328D2F-488A-4DBA-A0F4-96B56D2227F1 wds:Q37037658-FBF86C38-D391-40D2-9081-4B80A2EB8C79
cites work	METAL: fast and efficient meta-analysis of genomewide association scans Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. The genetics of central corneal thickness Collagen-related genes influence the glaucoma risk factor, central corneal thickness Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile Genetics and beyond--the transcriptome of human monocytes and disease susceptibility The number of people with glaucoma worldwide in 2010 and 2020 Keratoconus Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions A new mathematical model for relative quantification in real-time RT-PCR Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 Structural abnormalities of the cornea and lid resulting from collagen V mutations Mutations in PRDM5 in brittle cornea syndrome identify a pathway regulating extracellular matrix development and maintenance Brittle cornea syndrome associated with a missense mutation in the zinc-finger 469 gene. Blue sclera with and without corneal fragility (brittle cornea syndrome) in a consanguineous family harboring ZNF469 mutation (p.E1392X). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis Five years of GWAS discovery Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

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