The genetics of glaucoma: an update

IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration.

Clinical genetics·2018

Specific retinal phenotype in early IQCB1-related disease.

Eye (London, England)·2017

The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.

Clinical genetics·2016

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.

Clinical genetics·2015

Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

Clinical genetics·2015

Ultrasound biomicroscopy in the management of retinoblastoma.

Eye (London, England)·2011

Effectiveness of SLT in lowering IOP in steroid-induced glaucoma: a systematic review.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

Association between attention deficit hyperactivity disorder and keratoconus.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

Glaucoma and cognition: a systematic review and meta-analysis of cognitive metrics in glaucoma patients.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

Factors influencing graft survival in full-thickness skin grafts of the periocular region: a systematic review.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

Assessing referral quality in glaucoma care: a retrospective analysis of clinical data in optometrist and ophthalmologist referrals.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

Predictors and clinical outcomes of surgical intervention in pediatric orbital cellulitis.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Current cardiology reviews·2026

Establishment of the endocrine variant extractor and its clinical application in identifying a novel GATA3 mutation in HDR syndrome.

Frontiers in endocrinology·2026

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Orthopaedic journal of sports medicine·2026

Root cause discovery via permutations and Cholesky decomposition.

Journal of the Royal Statistical Society. Series B, Statistical methodology·2026

In-silico analysis of Bifidobacterium bifidum strain 900791 genome in the context of the B. bifidum pangenome.

Frontiers in cellular and infection microbiology·2026

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

The European journal of neuroscience·2026

Related Experiment Videos

The genetics of glaucoma: an update

Related Concept Videos

IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration.

Specific retinal phenotype in early IQCB1-related disease.

The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.

Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

Ultrasound biomicroscopy in the management of retinoblastoma.

Effectiveness of SLT in lowering IOP in steroid-induced glaucoma: a systematic review.

Association between attention deficit hyperactivity disorder and keratoconus.

Glaucoma and cognition: a systematic review and meta-analysis of cognitive metrics in glaucoma patients.

Factors influencing graft survival in full-thickness skin grafts of the periocular region: a systematic review.

Assessing referral quality in glaucoma care: a retrospective analysis of clinical data in optometrist and ophthalmologist referrals.

Predictors and clinical outcomes of surgical intervention in pediatric orbital cellulitis.

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Establishment of the endocrine variant extractor and its clinical application in identifying a novel <i>GATA3</i> mutation in HDR syndrome.

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Root cause discovery via permutations and Cholesky decomposition.

<i>In-silico</i> analysis of <i>Bifidobacterium bifidum</i> strain 900791 genome in the context of the <i>B. bifidum</i> pangenome.

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

Related Experiment Videos

The genetics of glaucoma: an update

Related Concept Videos

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