Molecular Vision 2012; 18:1526-1539 <>
Received 4 December 2011 | Accepted 9 June 2012 | Published 13 June 2012

Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma

Soo Park,1,4 Yalda Jamshidi,2 Daniela Vaideanu,3 Scott Fraser,3 Jane C. Sowden4

1Tennent Institute of Ophthalmology, Gartnavel General Hospital, Glasgow, UK; 2Human Genetics Research Centre, St George's University of London, UK; 3Ophthalmology Department, Sunderland Eye Infirmary, Sunderland, UK; 4Developmental Biology Unit, University College London Institute of Child Health and Great Ormond Street Hospital for Children NHS Trust, London, UK

Correspondence to: Dr J.C. Sowden, Developmental Biology Unit, UCL Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, United Kingdom; Phone: +44 (0) 207 905 2121; FAX: +44 (0) 207 7831 4366; email:


Purpose: Primary open-angle glaucoma (POAG) is a common but complex disease with a strong genetic component. Notably, few genes have been robustly associated with POAG. An obvious group of genes to test as susceptibility factors for POAG are the developmental genes forkhead box C1 (FOXC1), transforming growth factor-beta 2 (TGFβ2), and bone morphogenic protein 4 (BMP4). These genes are known to play important roles in the normal morphogenesis of the anterior segment and/or have been implicated in intra-ocular pressure (IOP) regulation and trabecular meshwork function. This study investigates the role of FOXC1, TGFβ2, and BMP4 in POAG.

Methods: The contribution of common genetic variation at the FOXC1, TGFβ2, and BMP4 loci to risk of POAG was investigated in a case-control association study in 330 British Caucasian individuals comprised of 272 high-tension glaucoma (HTG) and 58 ocular hypertension (OHT), and 276 matched controls.

Results: All the single nucleotide polymorphisms (SNPs) were in Hardy–Weinberg equilibrium and genotyping success rate was >92% for all SNPs. With the exception of a weak association between the BMP4 tagging SNP rs2761884 and the combined patient group HTG+OHT that did not withstand permutation testing (uncorrected p=0.0400, corrected p=0.1320), no associations (p<0.05) were identified between the patient groups (HTG and OHT) and FOXC1, TGFβ2, and BMP4 alleles and haplotypes compared to the control group.

Conclusions: This is the first association analysis of FOXC1, TGFβ2, and BMP4 and POAG. These genes were selected as candidate genes for POAG because of their biologic roles. No significant associations were identified between FOXC1, TGFβ2, and BMP4 alleles and haplotypes and POAG. The lack of association suggests that common variation in these genes do not have a significant role in the pathogenesis of POAG among British Caucasian subjects.


Glaucoma is a complex heterogeneous disorder characterized by an optic neuropathy in which progressive degeneration of retinal ganglion cells leads to excavation of the optic nerve head and to visual field loss. It is a major cause of visual impairment and blindness worldwide affecting approximately 67 million people [1]. Primary open-angle glaucoma (POAG), the most common form of glaucoma, has an estimated prevalence of 1.2% for the age group 40 to 89 years in the white UK population [2]. POAG is predominately composed of high-tension glaucoma, where the intraocular pressure (IOP) is raised (IOP >21 mmHg). Normal-tension glaucoma (NTG), which is another important but less common subgroup of POAG, is an optic neuropathy similar to HTG but the IOP levels are within the statistically normal range (IOP ≤21 mmHg). On the other hand, individuals with ocular hypertension (OHT) have raised IOP without clinical signs of glaucomatous optic neuropathy; however, OHT is an important risk factor for POAG, and 10% will convert to POAG over a 10-year period [3].

Although the proportion of genetically attributable cases of POAG is unknown, there is increasing evidence to suggest POAG has a significant heritable basis. Population-based studies have shown that a positive family history is an important risk factor for POAG. The relative risk of developing POAG among individuals with a positive family history varies from 3 to 10-fold [4,5]. Further evidence that genetic factors are important is supported by twin studies which have shown a higher degree of concordance among monozygotic twin [6,7]. In particular, Gottfredsdottir et al. [6] showed the concordance of open angle glaucoma in monozygotic twin pairs was significantly higher at 98% compared to their spouses (70%). Moreover, the prevalence of POAG is highest in black populations and lowest in northern Asian populations; these ethnic differences may be attributable to genetics among other factors [8]. Genetic linkage studies among rare pedigrees with Mendelian patterns of adult-onset POAG inheritance have identified 14 genetic loci (GLC1A-N) [9-19]. However, only 3 genes (myocilin, trabecular meshwork inducible glucocorticoid response [MYOC], optineurin [OPTN], and WD repeat domain 36 [WDR36]) have shown to be robustly associated with POAG in the general population. Furthermore, only MYOC (GLC1A) is established as directly causative, mutations of which account for 5% of POAG, while due to conflicting results the exact roles of OPTN (GLC1E) and WDR36 (GLC1G) in POAG remain uncertain [20,21]. A recent genome-wide association study involving 590 affected individuals with advanced POAG and 3,956 controls, has identified susceptible loci at transmembrane and coiled-coil domain-containing protein 1 (TMCO1) and CDKN2B antisense RNA 1 (non-protein coding; CDKN2B-AS1) for POAG [22]. Based on current knowledge, it is probable that POAG is a genetically heterogeneous disorder caused by the interaction between several genetic and environmental factors.

Genes that cause developmental glaucoma [23], with the exception of the cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) and LIM homeobox transcription factor 1, beta (LMX1B) genes, have yet to be assessed as genetic susceptibility factors for POAG. CYP1B1 causes primary congenital glaucoma and is also involved in cases of juvenile open-angle glaucoma [24]. A recent study has implicated a CYP1B1 polymorphism as a susceptibility factor for POAG [25]. LMX1B mutations, on the other hand, cause dominantly-inherited Nail-Patella Syndrome (NPS; OMIM 161200) in which approximately 33% of patients develop glaucoma [26]. More importantly, LMX1B haplotypes have shown to influence susceptibility to POAG [27].

Developmental glaucoma refers to glaucomas that are associated with developmental malformations of the anterior segment of the eye [28]. Anterior segment dysgenesis (ASD) may lead to incomplete development, or dysfunction, of the structures that form the aqueous drainage pathway, and can result in IOP elevation secondary to aqueous outflow obstruction, predisposing to glaucoma [23]. Existing studies indicate that developmental glaucoma genes forkhead box C1 (FOXC1), transforming growth factor-beta 2 (TGFβ2), and bone morphogenic protein 4 (BMP4) are strong candidate genes for POAG susceptibility. Foxc1 is expressed in the developing trabecular meshwork (TM) [29] whereas TGFβ2 and BMP4 are expressed in the adult human TM [30,31]. All of these genes cause developmental malformation of the anterior segment [29,32,33]. The essential role of these developmental glaucoma genes for the development of the anterior segment and in the development of TM implies that FOXC1, TGFβ2, and BMP4 are crucial for the normal development of drainage structures and preservation of normal IOP. This idea is supported by targeted heterozygous mutation in animal models resulting in malformation of the drainage structures [29,32,33] with a high incidence of glaucoma ranging from 40%–75% or above [33,34].

Elevated levels of TGFβ2 have been found in POAG patients. In addition, studies have shown that raised IOP in POAG is as a result of increased resistance to aqueous outflow [35] and this is associated with biochemical and morphological changes in the TM [36]. There is an accumulation of extracellular matrix (ECM) in the TM of glaucoma patients, and this may be as a result of disruption of the balance between ECM deposition and degradation [36]. In vitro studies have shown that TGFβ2 and BMP4 act in concert to maintain a balance between ECM deposition and degradation, and may play an important role in glaucoma pathogenesis through mis-regulation of ECM synthesis and cross-linkage of ECM components of the TM [30].

Since Foxc1 is expressed in the developing embryonic TM [29], mutations or altered expression of FOXC1 could interfere with normal function of the tissue and lead to increased risk of glaucoma. Although expression of FOXC1 is yet to be studied in adults, it is highly possible that continued expression of the abnormal gene product (from age-related, subclinical mutations) throughout life, or altered levels of expression of FOXC1 could interfere with normal function of the TM, thereby leading to increased risk of glaucoma through the effects of raised IOP. This notion is supported by the fact that glaucoma associated with mutations in the developmental glaucoma genes can present at any time from birth to adulthood, and in some instances above 70 years of age [37]. Furthermore, in some affected family members with glaucoma as a result of FOXC1 mutations, the anterior segment malformation may be very subtle, and easily missed in clinical examination [37,38], a feature more in keeping with POAG. In addition, the risk of developing glaucoma is not related to the severity of the phenotype [37], suggesting that subtle dysfunction of the angle drainage structures may be contributing toward glaucoma [39].

It is thus plausible that these developmental glaucoma genes contribute to age-related open angle glaucoma, where the ocular drainage structures have abnormalities that are not clinically visible but which cause dysfunction with age. We hypothesize that sub-clinical mutations/polymorphisms in FOXC1, TGFβ2, and BMP4 may produce subtle and undetected abnormalities in anterior segment structure and function, which predispose to glaucomatous optic neuropathy through the effects of raised IOP and may be a significant susceptibility factor for the development of OHT and POAG.

In this study, we assess whether variant alleles of FOXC1, TGFβ2, and BMP4 play a role in the general population. A case-control genetic association study was performed to compare the prevalence of FOXC1, TGFβ2, and BMP4 tagging single nucleotide polymorphisms (tSNPs) in three groups, HTG, OHT, and a normal control group. Haplotypes in FOXC1, TGFβ2, and BMP4 were identified and their prevalence assessed in patients with glaucomatous optic neuropathy (HTG patients) and in patients with raised IOP (HTG and OHT patients).


Recruitment of patients

All of the participating subjects were recruited from glaucoma outpatient clinics at the Sunderland Eye Infirmary in the North-East of England, UK, a secondary ophthalmology referral center. The research followed the tenets of the Declaration of Helsinki. Informed consent was obtained from all participants after the nature and possible consequences of the study were explained. The study had Local Research Ethics Committee approval. A cohort of HTG cases (n=272), and unrelated controls (n=276) matched for ethnicity, age and sex were recruited to the study. Cases with OHT (n=58) were also collected. All cases (n=330) and controls were of British Caucasian descent.

Control participants, either accompanying spouses or friends of individuals with glaucoma, were recruited randomly. All controls underwent a complete ophthalmic examination to exclude individuals with glaucoma from the control group, and were confirmed to have no visual complaints and IOP of <22 mmHg with a normal disc appearance. Individuals with a family history of glaucoma were excluded.

All case subjects underwent a complete ophthalmic examination as previously described (Park et al. [27]) including best visual acuity, and visual field testing using a Humphrey SITA standard 24–2 perimetry (Carl Zeiss Meditec AG, Jena, Germany), slit lamp examination of the anterior segment (including gonioscopy), measurement of IOP by Goldmann applanation tonometer, posterior segment examination of the retina and optic disc following pupil dilation and measurement of the cup-disc ratio (CDR). The clinical diagnosis (including assessment of visual fields) was made by the same consultant with a special interest in glaucoma and experience in anterior segment phenotyping. This ensured exclusion of individuals with glaucoma from the control group and made certain that cases were correctly classified either as HTG and OHT. Central corneal thickness (CCT) data was not collected for the cases and controls in the current study since a pachymeter was not available at the time when this study was performed. Adult individuals with a diagnosis of HTG or OHT after the age of 40 years were enrolled based on the following clinical criteria:

Presence of glaucomatous optic neuropathy (defined by loss of neuroretinal rim) with compatible and reproducible visual field loss for HTG, and absence of detectable glaucomatous damage or field loss for OHT. All of the visual field tests showed reproducible field defects that were compatible with the degree of glaucomatous cupping of the optic nerve head (defined by loss of neuroretinal rim), and were ensured to have a satisfactory reliability score of ≤20% fixation loss, false positive of ≤33% and/or false negative of ≤33%;

Open drainage angles on gonioscopy;

IOP consistently ≥22 mmHg on diurnal testing for HTG and OHT. To be certain that the participants were correctly assigned to the appropriate case groups, individuals with borderline IOPs (21–23 mmHg) were excluded from this study;

Absence of a secondary cause for glaucomatous optic neuropathy;

Absence of non-glaucomatous field losses and disc changes (i.e., high myopia).

Selection and analysis of single nucleotide polymorphisms

We employed a tagging single nucleotide polymorphism approach to screen FOXC1, TGFβ2, and BMP4 genes including 10 kb of upstream and downstream flanking region in patient and control groups using tSNPs selected from the HapMap database (HapMap Data Release #22/Phase II Apr 2007; Centre d'Etude du Polymorphisme Humain [CEPH] population). Genotypes of 90 CEU The Sequenom iPLEXTM Assay MassARRAY® (Sequenom, San Diego, CA) was used for high-throughput SNP genotyping (details of primer information used for SNP genotyping provided in Appendix 1). Allele frequencies for each SNP were tested for agreement with Hardy–Weinberg expectations (p>0.05) using a χ2 goodness-of-fit test.

A total of 5 tSNPs for BMP4 spanning a region of 15,272 bp (including the 4,814 bp BMP4 gene), 19 tSNPs for TGFβ2, spanning a region of 98,075 bp (including the 95,108 bp TGFβ2 gene), and 4 tSNPs for FOXC1 spanning a region of 12,012 bp (including the 1,661 bp FOXC1 gene) were selected from the HapMap database and genotyped in all individuals (Figure 1, Figure 2, and Figure 3).

LD and haplotype structure of the FOXC1, TGFβ2, and BMP4 genomic region

Haplotypes were inferred using Haploview v.4.0, and associations between tSNP or haplotype and glaucoma were investigated. The method of Gabriel et al. [40], as implemented in Haploview, was used to construct LD blocks from tSNPs with minor allele frequencies (MAF) ≥5%. LD between tSNPs was measured by the pairwise D' statistic and the LD structure was examined using the 80% confidence bounds of D' to define sites of historical recombination between tSNPs.

Haplotypes were constructed from genotype data in the full-size case-control panel within blocks by using an accelerated expectation-maximization algorithm method [41]. In each haplotype block, common haplotypes with frequencies ≥1% were inferred that accounted for >98% of the chromosomes. Differences in genotype and haplotype frequencies between cases and controls were determined using a χ2 distribution with 2 degrees of freedom. Permutation testing was performed to calculate corrected p-values for multiple testing with 1,000 simulations. Odds ratios (ORs) were calculated using THESIAS v.3.1 with 95% confidence intervals (CIs) for each genotype with the respective wild type as the reference. Thesias is based on the maximum likelihood model described in Tregouet et al. [42].

Using the Stata built-in power and sample size functions (Stata Statistical Software: Release 8.0; Stata Corporation, College Station, TX), a power of 80% was estimated using the sample size of 276 controls and 330 cases, to identify a difference in genotype and allele frequency between 10%–18% at a significance level of p<0.05 between the controls and cases.


Among the cases, 272 (74.3%) were classified as HTG, and 58 (15.6%) as OHT (Table 1). All tSNPs (Figure 1, Figure 2, and Figure 3) conformed to Hardy–Weinberg equilibrium and the genotyping success rate varied from 92.0% and 99.0%. The pairwise LD matrix revealed 2 main haplotype blocks for BMP4 (Figure 1) and 4 haplotype blocks for TGFβ2 (Figure 2). Haplotype analysis of FOXC1 revealed no common haplotype between patients and variants of FOXC1 (Figure 3) due to lack of LD between SNPs.

Lack of association between SNPs in TGFβ2, BMP4, and FOXC1 and POAG

The allele frequencies of the 19 tSNPs in TGFβ2, 5 tSNPs in BMP4 and 4 tSNPs in FOXC1 between the 3 separate case groups (HTG, OHT, HTG+OHT) and the controls were assessed. No significant associations were found between TGFβ2, BMP4, and FOXC1 and glaucoma (Table 2 [A], Table 3 [A], Table 4), except between the combined group HTG+OHT and BMP4 (Table 3 [A]) where there was a weak association which did not withstand permutation testing (uncorrected p=0.040, corrected p=0.1320, OR 1.26). In addition, these tSNPs were analyzed under 3 different genetic models (dominant, co-dominant and recessive models) and no significant associations were identified (data not shown).

Absence of association between haplotypes in TGFβ2 and BMP4 and HTG

The difference in the distribution of all common haplotypes in TGFβ2 and BMP4 (see Table 2 [B] and Table 3 [B]) between individuals with HTG and controls was assessed (but not for FOXC1 as common haplotypes were not present) and no significant haplotype associations were identified for each haplotype blocks. The absence of common haplotypes between patients and FOXC1 can be explained by the small size of the FOXC1 gene (3,447 bp), which makes it less likely that haplotype blocks are present in such a small region.

Absence of association between haplotypes in TGFβ2 and BMP4, and raised IOP (HTG+OHT)

Here, assessment for possible common haplotype associations between combined raised IOP patient group (HTG+OHT) and the controls were performed for TGFβ2 and BMP4 (see Table 2 [C] and Table 3 [C]) but not for FOXC1 as common haplotypes were not present and no significant haplotype effects for each haplotype block were found.


Despite recent progress in identifying genes associated with glaucoma, the contribution of genetics to the pathogenesis of POAG continues to remain unclear. Given the relatively high prevalence of POAG within the normal population, and the fact that it is amendable to treatment when detected early, identification of genetic risk factors would offer the prospect of early POAG diagnosis, in addition to the tailoring of appropriate treatments to those who would be most likely to benefit. However, such screening programs are currently limited by the paucity of the identified causative genes [43] and identification of the most significant disease-associated alleles in different populations is of paramount importance.

Recent work has started to investigate whether analysis of genetic risk in glaucoma can be progressed through the investigation of individual quantitative traits underlying disease risk- IOP, optic nerve cupping as measured by CDR, and CCT. For example, a recent study showed that both CDR and IOP have genetic components that correlate with POAG [44]. Wirtz et al. [15] proposed that searching for genes influencing POAG phenotype components may increase the power to dissect the genetic architecture of POAG. The question of whether the genetic etiology of POAG is determined by a large number of rare variants with major effects on the disease risk (rare variant, common disease hypothesis) or whether there are multiple common variants underlying the disease (common variant, common disease hypothesis) is also being addressed in new studies [45]. For example, based on a genome wide SNP analysis of a large cohort, Ramdas et al. [45] proposed a polygenic model for CDR.

Genes in which mutation causes anterior segment angle anomalies and glaucoma are strong candidates for glaucoma susceptibility and may contribute to glaucoma more frequently than expected, and possibly play an important role in the common form of POAG. In this study three candidate genes TGFβ2, BMP4, and FOXC1 were examined. Selection of these candidates was based existing knowledge of their function in the anterior segment.

In this study, despite the evidence that the candidate genes are involved in glaucoma disease pathways no significant associations were identified between TGFβ2, BMP4, and FOXC1 alleles and haplotypes and POAG in a population of patients and controls recruited form the North East of England. This represents the first association analysis of TGFβ2, BMP4, and FOXC1; the lack of association of common polymorphism does not provide evidence in support of the hypothesis that these genes play a significant genetic role in the pathogenesis of glaucoma among white British subjects.

A lack of association, however, should be interpreted with caution unless proven by investigating a substantially larger sample of the population. This is because of the small possibility of such results being caused by a false-negative error, which is confounded by the small size of the OHT sub-group. The key determinant of quality in an association study is the sample size since the power to detect an association depends partly on this as well as the size of the effect. If a study with negative results has insufficient power, an association is unlikely to be significant as there is a higher chance that it is a falsely negative result. For this study, with a sample size of 276 controls and 330 cases, an adequate study power of 80% was achieved if a difference in genotype and allele frequency was 10%–18% between controls and cases at a significance level of p<0.05. However, if the individual subgroups are considered, the OHT group (n=58) was clearly under-represented, despite being adequate to produce a robust result as being part of the whole cohort. In addition, the results obtained from this study reflect only one ethnic group (in this case white British adults) and not other ethnicities and it would need to be confirmed if other ethnic groups showed the same results.

One of the limitations of this study is the absence of CCT measurement. In the current study, IOP measurements were checked by a Tono-Pen which is less affected by CCT [46], in addition to performing applanation tonometry. Two recent studies that adjusted IOP for CCT found that the correction did not alter the diagnosis of HTG or NTG [47], and did not affect the relationship between the prevalence of POAG and IOP respectively [48]. Furthermore, to be certain that the participants were correctly assigned to the appropriate case groups, individuals with borderline IOPs (21–23 mmHg) were excluded from this study. Even if a correction formulae were to be applied with a 10 µm change in the corneal thickness inducing a 0.2 mmHg change in IOP reading [49], a 2–3 mmHg IOP change (which would include the excluded individuals within the borderline IOP) would induce a 100–150 µm change in the CCT, which is a considerable amount. Hence, it is still highly unlikely that the individuals with IOPs of 20 mmHg or below or IOPs of 24 mmHg or higher would have their diagnosis altered (assuming that the average CCT is approximately 537–550 µm) [50] since these subjects would be required to have either an abnormally thin corneas or an unusually thick corneas.

In summary, this study did not demonstrate any significant allelic or haplotype associations between TGFβ2, BMP4, and FOXC1 and OHT/POAG. It is hence concluded that common variants in the TGFβ2, BMP4, and FOXC1 genes do not play a major role in the genetic etiology of POAG in the population investigated.

Appendix 1. Primer information.


This work was supported by the Royal College of Surgeons of Edinburgh, Alcon Laboratories (UK) Limited, and the Ulverscroft Foundation. J.C.S. is supported by Great Ormond Street Hospital Children's Charity.


  1. Quigley HA. Number of people with glaucoma worldwide. Br J Ophthalmol. 1996; 80:389-93. [PMID: 8695555]
  2. Tuck MW, Crick RP. The age distribution of primary open angle glaucoma. Ophthalmic Epidemiol. 1998; 5:173-83. [PMID: 9894803]
  3. Kass MA, Heuer DK, Higginbotham EJ, Johnson CA, Keltner JL, Miller JP, Parrish RK, , 2nd Wilson MR, Gordon MO. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002; 120:701-13. [PMID: 12049574]
  4. Tielsch JM, Katz J, Sommer A, Quigley HA, Javitt JC. Family history and risk of primary open angle glaucoma. The Baltimore Eye Survey. Arch Ophthalmol. 1994; 112:69-73. [PMID: 8285897]
  5. Wolfs RC, Klaver CC, Ramrattan RS, van Duijn CM, Hofman A, de Jong PT. Genetic risk of primary open-angle glaucoma: population-based familial aggregation study. Arch Ophthalmol. 1998; 116:1640-5. [PMID: 9869795]
  6. Gottfredsdottir MS, Sverrisson T, Musch DC, Stefansson E. Chronic open-angle glaucoma and associated ophthalmic findings in monozygotic twins and their spouses in Iceland. J Glaucoma. 1999; 8:134-9. [PMID: 10209731]
  7. Teikari JM. Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study. Acta Ophthalmol (Copenh). 1987; 65:715-20. [PMID: 3434238]
  8. Kosoko-Lasaki O, Gong G, Haynatzki G, Wilson MR. Race, ethnicity and prevalence of primary open-angle glaucoma. J Natl Med Assoc. 2006; 98:1626-9. [PMID: 17052053]
  9. Monemi S, Spaeth G, DaSilva A, Popinchalk S, Ilitchev E, Liebmann J, Ritch R, Héon E, Crick RP, Child A, Sarfarazi M. Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet. 2005; 14:725-33. [PMID: 15677485]
  10. Sarfarazi M, Child A, Stoilova D, Brice G, Desai T, Trifan OC, Poinoosawmy D, Crick RP. Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region. Am J Hum Genet. 1998; 62:641-52. [PMID: 9497264]
  11. Sheffield VC, Stone EM, Alward WL, Drack AV, Johnson AT, Streb LM, Nichols BE. Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31. Nat Genet. 1993; 4:47-50. [PMID: 8513321]
  12. Stoilova D, Child A, Trifan OC, Crick RP, Coakes RL, Sarfarazi M. Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region. Genomics. 1996; 36:142-50. [PMID: 8812425]
  13. Trifan OC, Traboulsi EI, Stoilova D, Alozie I, Nguyen R, Raja S, Safarazi M. A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region. Am J Ophthalmol. 1998; 126:17-28. [PMID: 9683145]
  14. Wirtz MK, Samples JR, Kramer PL, Rust K, Topinka JR, Yount J, Koler RD, Acott TS. Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q. Am J Hum Genet. 1997; 60:296-304. [PMID: 9012402]
  15. Wirtz MK, Samples JR, Rust K, Lie J, Nordling L, Schilling K, Acott TS, Kramer PL. GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36. Arch Ophthalmol. 1999; 117:237-41. [PMID: 10037570]
  16. Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Evidence for a novel glaucoma locus at chromosome 3p21–22. Hum Genet. 2005; 117:249-57. [PMID: 15906098]
  17. Pang CP, Fan BJ, Canlas O, Wang DY, Dubois S, Tam PO, Lam DS, Raymond V, Ritch R. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q. Mol Vis. 2006; 12:85-92. [PMID: 16518310]
  18. Wang DY, Fan BJ, Chua JK, Tam PO, Leung CK, Lam DS, Pang CP. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q. Invest Ophthalmol Vis Sci. 2006; 47:5315-21. [PMID: 17122119]
  19. Wiggs JL, Lynch S, Ynagi G, Maselli M, Auguste J, Del Bono EA, Olson LM, Haines JL. A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12. Am J Hum Genet. 2004; 74:1314-20. [PMID: 15108121]
  20. Alward WL, Kwon YH, Kawase K, Craig JE, Hayreh SS, Johnson AT, Khanna CL, Yamamoto T, Mackey DA, Roos BR, Affatigato LM, Sheffield VC, Stone EM. Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma. Am J Ophthalmol. 2003; 136:904-10. [PMID: 14597044]
  21. Wiggs JL, Auguste J, Allingham RR, Flor JD, Pericak-Vance MA, Rogers K, LaRocque KR, Graham FL, Broomer B, Del Bono E, Haines JL, Hauser M. Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol. 2003; 121:1181-3. [PMID: 12912697]
  22. Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, Mills RA, Danoy P, Casson R, Viswanathan AC, Liu JZ, Landers J, Henders AK, Wood J, Souzeau E, Crawford A, Leo P, Wang JJ, Rochtchina E, Nyholt DR, Martin NG, Montgomery GW, Mitchell P, Brown MA, Mackey DA, Craig JE. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B–AS1. Nat Genet. 2011; 43:574-8. [PMID: 21532571]
  23. Gould DB, Smith RS, John SW. Anterior segment development relevant to glaucoma. Int J Dev Biol. 2004; 48:1015-29. [PMID: 15558492]
  24. Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Am J Hum Genet. 2002; 70:448-60. [PMID: 11774072]
  25. Bhattacharjee A, Banerjee D, Mookherjee S, Acharya M, Banerjee A, Ray A, Sen A. Indian Genome Variation Consortium, Ray K. Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis. 2008; 14:841-50. [PMID: 18483560]
  26. Mimiwati Z, Mackey DA, Craig JE, Mackinnon JR, Rait JL, Liebelt JE, Ayala-Lugo R, Vollrath D, Richards JE. Nail-patella syndrome and its association with glaucoma: a review of eight families. Br J Ophthalmol. 2006; 90:1505-9. [PMID: 16825280]
  27. Park S, Jamshidi Y, Vaideanu D, Bitner-Glindzicz M, Fraser S, Sowden JC. Genetic risk for primary open angle glaucoma determined by LMX1B haplotypes. Invest Ophthalmol Vis Sci. 2009; 50:1522-30. [PMID: 18952915]
  28. Gould DB, John SW. Anterior segment dysgenesis and the developmental glaucomas are complex traits. Hum Mol Genet. 2002; 11:1185-93. [PMID: 12015278]
  29. Smith RS, Zabaleta A, Kume T, Savinova OV, Kidson SH, Martin JE, Nishimura DY, Alward WL, Hogan BL, John SW. Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development. Hum Mol Genet. 2000; 9:1021-32. [PMID: 10767326]
  30. Wordinger RJ, Fleenor DL, Hellberg PE, Pang IH, Tovar TO, Zode GS, Fuller JA, Clark AF. Effects of TGF-beta2, BMP-4, and gremlin in the trabecular meshwork: implications for glaucoma. Invest Ophthalmol Vis Sci. 2007; 48:1191-200. [PMID: 17325163]
  31. Wordinger RJ, Clark AF, Agarwal R, Lambert W, McNatt L, Wilson SE, Qu Z, Fung BK. Cultured human trabecular meshwork cells express functional growth factor receptors. Invest Ophthalmol Vis Sci. 1998; 39:1575-89. [PMID: 9699547]
  32. Saika S, Saika S, Liu CY, Azhar M, Sanford LP, Doetschman T, Gendron RL, Kao CW, Kao WW. TGFbeta2 in corneal morphogenesis during mouse embryonic development. Dev Biol. 2001; 240:419-32. [PMID: 11784073]
  33. Chang B, Smith RS, Peters M, Savinova OV, Hawes NL, Zabaleta A, Nusinowitz S, Martin JE, Davisson ML, Cepko CL, Hogan BL, John SW. Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure. BMC Genet. 2001; 2:18 [PMID: 11722794]
  34. Strungaru MH, Dinu I, Walter MA. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations. Invest Ophthalmol Vis Sci. 2007; 48:228-37. [PMID: 16693611]
  35. Grant WM. Open-Angle Glaucoma Associated with Vitreous Filling the Anterior Chamber. Trans Am Ophthalmol Soc. 1963; 61:196-218. [PMID: 6413918]
  36. Rohen JW. Why is intraocular pressure elevated in chronic simple glaucoma? Anatomical considerations. Ophthalmology. 1983; 90:758-65. [PMID: 6676983]
  37. Shields MB. Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome. Trans Am Ophthalmol Soc. 1983; 81:736-84. [PMID: 12766066]
  38. Lehmann OJ, Tuft S, Brice G, Smith R, Blixt A, Bell R, Johansson B, Jordan T, Hitchings RA, Khaw PT, John SW, Carlsson P, Bhattacharya SS. Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function. Invest Ophthalmol Vis Sci. 2003; 44:2627-33. [PMID: 6871144]
  39. Chisholm IA, Chudley AE. Autosomal dominant iridogoniodysgenesis with associated somatic anomalies: four-generation family with Rieger's syndrome. Br J Ophthalmol. 1983; 67:529-34. [PMID: 17197537]
  40. Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C. The structure of haplotype blocks in the human genome. Science. 2002; 296:2225-9. [PMID: 12029063]
  41. Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005; 21:263-5. [PMID: 15297300]
  42. Tregouet DA, Barbaux S, Escolano S, Tahri N, Golmard JL, Tiret L, Cambien F. Specific haplotypes of the P-selectin gene are associated with myocardial infarction. Hum Mol Genet. 2002; 11:2015-23. [PMID: 12165563]
  43. Fan BJ, Tam PO, Choy KW, Wang DY, Lam DS, Pang CP. Molecular diagnostics of genetic eye diseases. Clin Biochem. 2006; 39:231-9. [PMID: 16412407]
  44. Charlesworth J, Kramer PL, Dyer T, Diego V, Samples JR, Craig JE, Mackey DA, Hewitt AW, Blangero J, Wirtz MK. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness. Invest Ophthalmol Vis Sci. 2010; 51:3509-14. [PMID: 20237253]
  45. Ramdas WD, Amin N, van Koolwijk LM, Janssens AC, Demirkan A, de Jong PT, Aulchenko YS, Wolfs RC, Hofman A, Rivadeneira F. Uitterlinden. Genetic architecture of open angle glaucoma and related determinants. J Med Genet. 2011; 48:190-6. [PMID: 21059592]
  46. Bhan A, Browning AC, Shah S, Hamilton R, Dave D, Dua HS. Effect of corneal thickness on intraocular pressure measurements with the pneumotonometer, Goldmann applanation tonometer, and Tono-Pen. Invest Ophthalmol Vis Sci. 2002; 43:1389-92. [PMID: 11980851]
  47. Miyazawa A, Fuse N, Mengkegale M, Ryu M, Seimiya M, Wada Y, Nishida K. Association between primary open-angle glaucoma and WDR36 DNA sequence variants in Japanese. Mol Vis. 2007; 13:1912-9. [PMID: 17960130]
  48. Francis BA, Varma R, Chopra V, Lai MY, Shtir C, Azen SP. Intraocular Pressure, Central Corneal Thickness, and Prevalence of Open-Angle Glaucoma: The Los Angeles 49. Latino Eye Study. Am J Ophthalmol. 2008; 146:741-6. [PMID: 18672218]
  49. Doughty MJ, Zaman ML. Human corneal thickness and its impact on intraocular pressure measures: a review and meta-analysis approach. Surv Ophthalmol. 2000; 44:367-408. [PMID: 10734239]
  50. Shah S, Chatterjee A, Mathai M, Kelly SP, Kwartz J, Henson D, McLeod D. Relationship between corneal thickness and measured intraocular pressure in a general ophthalmology clinic. Ophthalmology. 1999; 106:2154-60. [PMID: 10571352]