Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment. (scientific article published in August 2012)

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

Q24312705

Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma

Q24657994

The human PAX6 gene is mutated in two patients with aniridia

Q28207886

Adult-onset primary open-angle glaucoma caused by mutations in optineurin

Q28217964

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

Q28273225

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

Q28298470

Reduction of intraocular pressure and glaucoma progression: results from the Early Manifest Glaucoma Trial

Q31113402

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

Q34005664

Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1.

Q34389060

Identification of a gene that causes primary open angle glaucoma.

Q34414141

The definition and classification of glaucoma in prevalence surveys

Q34508710

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

Q35569618

Complex genetics of complex traits: the case of primary open-angle glaucoma

Q36548759

Null mutations in LTBP2 cause primary congenital glaucoma

Q37189121

Prevalence and predictors of open-angle glaucoma: results from the visual impairment project

Q39585968

Factors affecting awareness and knowledge of glaucoma among patients presenting to an urban emergency department

Q39596075

How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania

Q40137352

Family history and risk of primary open angle glaucoma. The Baltimore Eye Survey

Q42611498

Prevalence of myocilin gene mutations in a novel UK cohort of POAG patients.

Q42619373

Open-angle glaucoma and ocular hypertension: the Long Island Glaucoma Case-control Study

Q42640292

Profiling of WDR36 missense variants in German patients with glaucoma

Q42641301

Prevalence of open-angle glaucoma in Australia. The Blue Mountains Eye Study

Q42641509

Analyses of reported family history of glaucoma: a preliminary investigation. The Barbados Eye Study Group

Q42646119

The 'GIST' score: ranking glaucoma for genetic studies. Glaucoma Inheritance Study of Tasmania

Q42648811

Bias in self-reported family history and relationship to glaucoma: the Blue Mountains Eye Study

Q42692728

Risk factors for first presentation of glaucoma with significant visual field loss

Q43924634

P433

issue

P921

main subject

New Zealand

Q664

P304

page(s)

569-575

P577

publication date

2012-08-01

P1433

published in

Clinical and Experimental Ophthalmology

Q15762228

P1476

title

Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment.

P478

volume

Reverse relations

cites work (P2860)

Q35990614	A novel de novo Myocilin variant in a patient with sporadic juvenile open angle glaucoma.
Q35918465	Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma
Q49958175	Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Q36949631	Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration.
Q21559610	Association of genetic variants with primary angle closure glaucoma in two different populations
Q34698471	Association of open-angle glaucoma loci with incident glaucoma in the Blue Mountains Eye Study
Q35099064	CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma
Q36511580	Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucoma
Q35164716	Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma
Q47561732	DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Q37037658	Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Q57251981	Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Q41077958	Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
Q35819272	Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy
Q52984879	Mice Homozygous for a Deletion in the Glaucoma Susceptibility Locus INK4 Show Increased Vulnerability of Retinal Ganglion Cells to Elevated Intraocular Pressure.
Q92784849	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Q64457826	Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based Studies
Q52606261	PAX6 molecular analysis and genotype-phenotype correlations in families with aniridia from Australasia and Southeast Asia.
Q47811572	Predictive genetic testing experience for myocilin primary open-angle glaucoma using the Australian and New Zealand Registry of Advanced Glaucoma.
Q64457814	Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Q93101966	Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
Q37427218	Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma.
Q39680619	The IRIS® Registry : Purpose and perspectives
Q40711802	The IRIS® Registry : Purpose and perspectives. German Version
Q36298531	Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma.

P356	DOI	10.1111/J.1442-9071.2011.02742.X
P698	PubMed publication ID	22171965