Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. - Wikidata - wikimedia - TriplyDB

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

http://www.wikidata.org/entity/Q34263078

about

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma Novel Insights into the Role of Long Noncoding RNA in Ocular Diseases An Updated Review on the Genetics of Primary Open Angle Glaucoma Regulation of intraocular pressure by soluble and membrane guanylate cyclases and their role in glaucoma Advances in the genomics of common eye diseases The role of cerebrospinal fluid pressure in glaucoma and other ophthalmic diseases: A review Precise long non-coding RNA modulation in visual maintenance and impairment Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma Spink2 modulates apoptotic susceptibility and is a candidate gene in the Rgcs1 QTL that affects retinal ganglion cell death after optic nerve damage Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region Presence and Risk Factors for Glaucoma in Patients with Diabetes.Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma.A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma.Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing.Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study.Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma.A survey of preoperative blood tests in primary open-angle glaucoma patients versus cataract surgery patients Primary cilia signaling mediates intraocular pressure sensation.Genome-wide association studies: applications and insights gained in Ophthalmology.CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies.Cerebrospinal fluid pressure decreases with older age.Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.Association of glutathione S transferases polymorphisms with glaucoma: a meta-analysis Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci Association of open-angle glaucoma loci with incident glaucoma in the Blue Mountains Eye Study DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma.Common and rare genetic risk factors for glaucoma.Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure.Corneal biomechanical properties and glaucoma-related quantitative traits in the EPIC-Norfolk Eye Study.The genetics of POAG in black South Africans: a candidate gene association study.The pathophysiology and treatment of glaucoma: a review.TBK1 gene duplication and normal-tension glaucoma.Association of MYOC and APOE promoter polymorphisms and primary open-angle glaucoma: a meta-analysis.Extracting Primary Open-Angle Glaucoma from Electronic Medical Records for Genetic Association Studies A common variant near TGFBR3 is associated with primary open angle glaucoma.

P2860

Q24263464-BC469115-3C8F-4B53-98C3-5278627C4897 Q26752617-89524598-F582-48BD-B874-83C37023004F Q26774468-1ACD79E4-11E2-495C-81C9-6EE28C72C7A9 Q26861763-80867748-0920-4127-863A-13DB09CBB3F6 Q27008236-C9FFC029-07FB-4E46-9840-319D313ED3CC Q27014349-4C1FC82C-E377-417C-80AC-B3A9E8A4F7C0 Q28071712-C64D208A-C2D1-4D0E-AD76-DDE0E7724D85 Q28392307-49D759E4-C638-4D4A-84F3-00B32917F32B Q28394939-0CBD54F7-0578-430E-B5B6-C5F7928B1EFF Q28506021-613EB1BB-314B-4C55-B5FE-316201BE30C2 Q28572262-B1FC573B-9826-4ACF-AC20-7B1FEE13E2EB Q30244246-82CCC31E-6CAD-4089-B67C-FD9045ACA298 Q33582113-7DAF662A-3573-4447-BC3B-D976FCE2D866 Q33649345-DCEED0DE-A55A-43F5-A03C-B69ACCD57C03 Q33686107-13496F13-F8E6-4690-8717-19B5C851EAE8 Q33759127-530A6FCB-ED50-4C8A-BCCE-284D3DEDF07F Q33790443-9530C69E-CEE8-425D-B5F4-37B0BA71ECB8 Q33854304-8F5A4DA7-169F-47EC-A998-F398EC5290A8 Q33906989-A414EE7A-6696-4019-9FB0-84973D47DCE0 Q33997990-A3542691-07DD-44F7-9743-97E0FF589D46 Q34144583-6B8557A4-C1BA-4E4C-BF31-3CFB40264828 Q34200382-B2936F61-5725-4576-B226-3B3F0D49862E Q34325988-4EFA92D1-C03A-469E-82AF-11A65E1DE6C1 Q34541003-EA406F91-8B46-4438-8BE3-EC0C64DF987E Q34555458-C0288AFF-FE6A-4244-9A7D-6E0E1046FEB4 Q34559060-AC4C8581-90EA-4D3A-A4E5-09A740AE1548 Q34562619-337AAC89-BDE4-4F8B-A36D-1B893F4984ED Q34639285-1C600990-16E1-4636-B04E-3078D962BB98 Q34698471-6ECAA3A3-89CF-4B74-AD97-D17BAFF27704 Q34741765-45B10038-9EA1-43B8-8588-19F44009C967 Q34754791-2ED8FBC8-8386-4C3C-A0F9-B13C21870456 Q34930464-C3944C8C-38DE-477A-91DD-E034F9EFD775 Q34999831-20EBBEC3-5675-498D-AA60-5BA6F97FAB1A Q35066210-B9F95DF2-18BB-4FE9-965C-8993C03368D8 Q35070093-E16D2296-3451-4663-A82D-8A7F3D07315C Q35168230-985DC65B-7C0C-4FA9-AF2D-C16B47FED9C2 Q35214246-A120DC44-5FE3-405A-9A62-1C399E7CFF32 Q35479865-E7A99668-707E-43DC-B599-458D58DE8C99 Q35659755-4593D67B-1496-43F3-A152-40F1CE636CE0 Q35693931-AC88626D-CC3E-4CB6-ABD4-AD237D504D35

P2860

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

http://www.wikidata.org/entity/Q34263078

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@ast

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@en

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@nl

type

label

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@ast

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@en

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@nl

prefLabel

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@ast

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@en

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@nl

P1433

Q34263078-5CCD4355-BE2F-43B6-BAF9-24B1E06ADC71

P1476

Q34263078-BC55C2A3-9749-4502-A64E-A0935AA1C248

P2093

Q34263078-060A6BAD-B78A-4820-932F-4546158FCEE7

Q34263078-0BD1D8C8-1D0D-4CB6-A48E-A8661ECD4373

Q34263078-1357F028-AF5E-4907-93F9-51875F22021B

Q34263078-1FDB0140-5A6D-4620-BE7E-AC34E99C9EF3

Q34263078-2D2F6E7D-F732-4246-AE66-B51E7FA29E33

Q34263078-335FE47D-0E55-49AC-AF33-CAAAF3920E4D

Q34263078-33628967-4CC5-462A-9C7A-2E45CC526F02

Q34263078-3ABD89A8-0100-4875-951E-18256F595AE1

Q34263078-4207D076-7DC3-47EE-96F5-2973AA942241

Q34263078-4262AF83-67D1-4162-9610-22534CBD8592

P2860

Q34263078-02DCBF63-3828-4A9E-BDB0-693D7AD00AD0

Q34263078-0F5EB436-661C-40D0-AFF7-84A3EFDE90AC

Q34263078-17AEB15D-21E0-4C86-B506-CA93A3CDFBA4

Q34263078-18E4FCA2-AF86-45D9-B224-DBF66E0D01D6

Q34263078-19848D7E-B2F0-4FEB-B885-CCE8282C9BF4

Q34263078-19CE6DD6-8CAC-452C-9640-660D53715B3C

Q34263078-1E5D3BAD-47DD-485F-8D10-CA96A3687694

Q34263078-1EA7A5D4-4760-41CF-8CAF-B6CE6F7F9E72

Q34263078-215F732C-DBF4-482E-9EDD-BD6F2E05D574

Q34263078-356FD194-AB09-4840-82CD-727B22BC3C94

P304

Q34263078-09AC6E62-71D0-4114-9F75-B05FA390A6EF

P31

Q34263078-DEE6D042-C8C5-4E4B-8E7B-FBC036181434

Q34263078-bfd38124-5c62-4968-ac56-5461e33131c8

P356

Q34263078-B893302F-2CE0-470D-ABE3-E0A36E0B1AA2

P433

Q34263078-52F75CAB-F577-4B2C-A9BF-6DEBAAEAB520

P478

Q34263078-1878CE21-FCCE-4731-AE9E-9DF4D4458ED8

P50

Q34263078-01C46B2E-458A-43FE-8158-4023C3703F8B

Q34263078-2C9B7369-8079-47FC-A0CA-3211D853128B

Q34263078-337C7D4F-019C-4FBF-B007-9FB5B8A8D9B1

Q34263078-3CAA7D33-8D09-455C-AB19-5BF0923BBE04

Q34263078-3EF8E177-CCF6-49D3-98B4-5265598F575A

Q34263078-3FA06C74-2997-45F6-8A0C-5723B1763508

Q34263078-6C3255B2-C269-446F-97AC-E89340DDA718

Q34263078-86FDAB7D-DCA4-4852-AD69-3DCD8729E6E2

Q34263078-A0A79F43-85AF-45D7-AB77-089925B9A900

Q34263078-A2BA7419-444D-49BA-82DC-D2136D43DF5F

P577

Q34263078-A8FFE380-6EF5-4CDF-BDFA-52F8F8D742DD

P5875

Q34263078-C490DD70-93F7-4C8C-965E-1E732D88E328

P698

Q34263078-DC357E2E-10A5-4D67-A7B3-7860BC33C7E6

P932

Q34263078-5572C0AC-30E3-4682-A8F5-C70A801BDC98

P356

JOURNAL.PGEN.1002654

P1433

P1476

Common variants at 9p21 and 8q ...... erve degeneration in glaucoma.

@en

P2093

Andrew Crenshaw

http://www.w3.org/2001/XMLSchema#string

Anthony Realini

http://www.w3.org/2001/XMLSchema#string

Cathy Laurie

http://www.w3.org/2001/XMLSchema#string

Cathy McCarty

http://www.w3.org/2001/XMLSchema#string

Dan Y Wang

http://www.w3.org/2001/XMLSchema#string

Daniel Mirel

http://www.w3.org/2001/XMLSchema#string

David C Musch

http://www.w3.org/2001/XMLSchema#string

David S Friedman

http://www.w3.org/2001/XMLSchema#string

Donald L Budenz

http://www.w3.org/2001/XMLSchema#string

Douglas Gaasterland

http://www.w3.org/2001/XMLSchema#string

P2860

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

ST7 is a novel low-density lipoprotein receptor-related protein (LRP) with a cytoplasmic tail that interacts with proteins related to signal transduction pathways

p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

PLINK: a tool set for whole-genome association and population-based linkage analyses

The number of people with glaucoma worldwide in 2010 and 2020

Whole-genome genotyping

Tsc-22 enhances TGF-beta signaling by associating with Smad4 and induces erythroid cell differentiation

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

P304

e1002654

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PGEN.1002654

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

8

http://www.w3.org/2001/XMLSchema#string

P50

Joel S. Schuman

Margaret A. Pericak-Vance

Robert N Weinreb

Terry Gaasterland

Joseph Caprioli

P577

2012-04-26T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

224926509

http://www.w3.org/2001/XMLSchema#string

P698

22570617

http://www.w3.org/2001/XMLSchema#string

P932

3343074

http://www.w3.org/2001/XMLSchema#string