Tiger Zhou

发表

Congenital glaucoma with anterior segment dysgenesis in individuals with biallelic CPAMD8 variants

D. Mackey, A. Hewitt, L. Kearns, 2018, bioRxiv.

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

J. Haines, P. Mitchell, L. Pasquale, 2018, Scientific Reports.

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

D. Mackey, J. Rait, A. Hewitt, 2017, European Journal of Human Genetics.

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

Xiaorong Liu, S. Maurer-Stroh, D. Mackey, 2016, The Journal of clinical investigation.

Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma.

D. Mackey, A. Hewitt, L. Kearns, 2020, Ophthalmology.

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

D. Mackey, J. Rait, A. Hewitt, 2017, European Journal of Human Genetics.

A novel GSN variant outside the G2 calcium‐binding domain associated with Amyloidosis of the Finnish type

R. Mills, E. Souzeau, J. Craig, 2021, Human mutation.

Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma.

M. Brown, D. Mackey, S. Graham, 2017, Investigative ophthalmology & visual science.

Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent

R. Mills, E. Souzeau, J. Craig, 2018, PloS one.

Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent.

M. Brown, R. Mills, E. Souzeau, 2017, Investigative ophthalmology & visual science.

RNA Sequencing of Lens Capsular Epithelium Implicates Novel Pathways in Pseudoexfoliation Syndrome

R. Mills, E. Souzeau, J. Craig, 2022, Investigative ophthalmology & visual science.

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

J. Haines, C. Klaver, P. Mitchell, 2020, Nature Genetics.

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

N. Martin, G. Montgomery, J. Beesley, 2018, Nature Genetics.

Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology.

D. Mackey, P. Khaw, P. Foster, 2019, Human molecular genetics.

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

J. Haines, P. Mitchell, L. Pasquale, 2018, Scientific Reports.

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Janey L. Wiggs, Paul Mitchell, Jonathan L. Haines, 2014, Nature Genetics.

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

Adriana I. Iglesias, A. Hofman, A. Uitterlinden, 2017, Human molecular genetics.

Deep Learning-based Identification of Intraocular Pressure-Associated Genes Influencing Trabecular Meshwork Cell and Organelle Morphology

S. Tran, D. Mackey, A. Hewitt, 2023, bioRxiv.

Occurrence of CYP1B1 Mutations in Juvenile Open-Angle Glaucoma With Advanced Visual Field Loss.

D. Mackey, I. Goldberg, A. Hewitt, 2015, JAMA ophthalmology.

Novel protein constituents of pathological ocular pseudoexfoliation syndrome deposits identified with mass spectrometry

N. Voelcker, R. Mills, J. Craig, 2018, Molecular vision.

Predictive genetic testing experience for myocilin primary open-angle glaucoma using the Australian and New Zealand Registry of Advanced Glaucoma

E. Souzeau, J. Craig, K. Burdon, 2014, Genetics in Medicine.

CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma

D. Mackey, L. Kearns, E. Souzeau, 2015, Molecular vision.

Occurrence of CYP 1 B 1 Mutations in Juvenile Open-Angle GlaucomaWith Advanced Visual Field Loss

D. Mackey, I. Goldberg, A. Hewitt, 2015 .

CYP 1 B 1 copy number variation is not a major contributor to primary congenital glaucoma

D. Mackey, L. Kearns, E. Souzeau, 2015 .

Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in MYRF

E. Souzeau, J. Craig, J. Breen, 2019, Molecular vision.

Rare variants in optic disc area gene CARD10 enriched in primary open‐angle glaucoma

M. Brown, D. Mackey, S. Graham, 2016, Molecular genetics & genomic medicine.

Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma.

P. Mitchell, Jie-Jin Wang, D. Mackey, 2016, Investigative ophthalmology & visual science.

Genetic Association at the 9 p 21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma

P. Mitchell, Jie-Jin Wang, D. Mackey, 2016 .

Meta‐analysis of Genome‐Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

Adriana I. Iglesias, A. Hofman, A. Uitterlinden, 2015, Genetic epidemiology.

Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma.

D. Mackey, S. Graham, A. Hewitt, 2015, American journal of ophthalmology.

High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucoma

D. Mackey, A. Hewitt, A. Senabouth, 2023, bioRxiv.

Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma

Tiger Zhou, Stuart MacGregor, Stuart Graham, 2017, PloS one.

Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent.

M. Brown, R. Mills, E. Souzeau, 2017, Investigative ophthalmology & visual science.

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

Xiaorong Liu, S. Maurer-Stroh, D. Mackey, 2016, The Journal of clinical investigation.

High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucoma

A. Hewitt, A. Senabouth, O. Siggs, 2024, Human molecular genetics.

Deep Learning-Based Identification of Intraocular Pressure-Associated Genes Influencing Trabecular Meshwork Cell Morphology

A. Hewitt, O. Siggs, Kristof Wing, 2024, Ophthalmology Science.