List of works - Zheng Li

A Genetic Variant in TGFBR3-CDC7 Is Associated with Visual Field Progression in Primary Open-Angle Glaucoma Patients from Singapore.

scientific article published on 14 September 2015

A Survey of DNA Variation ofC2ORF71in Probands with Progressive Autosomal Recessive Retinal Degeneration and Controls

scientific article published on 30 March 2011

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

scientific article

A common variant near TGFBR3 is associated with primary open angle glaucoma.

scientific article published on 10 April 2015

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.

scientific article

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy

scientific article

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene

scientific article published on 19 October 2011

Analysis of full length ADAMTS6 transcript reveals alternative splicing and a role for the 5' untranslated region in translational control.

scientific article published on October 2005

Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retina

scientific article published on December 2011

Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract

scientific article published on 11 December 2020

Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalpha.

scientific article published on April 2003

Expression of mutant and wild-type TIMP3 in primary gingival fibroblasts from Sorsby's fundus dystrophy patients

scientific article published on 01 May 2003

FGF-2 release from the lens capsule by MMP-2 maintains lens epithelial cell viability.

scientific article published on 15 August 2007

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

scientific article

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

scientific article

Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies

scientific article published on 06 June 2019

Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).

scientific article

Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus).

scientific article published on 29 April 2011

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

scientific article published on 17 October 2010

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

scientific article

TIMP3 mutation in Sorsby's fundus dystrophy: molecular insights

scientific article

The spatial organization of intra-tumour heterogeneity and evolutionary trajectories of metastases in hepatocellular carcinoma

scientific article published on 27 February 2017

List of works by Zheng Li

A Genetic Variant in TGFBR3-CDC7 Is Associated with Visual Field Progression in Primary Open-Angle Glaucoma Patients from Singapore.

A Survey of DNA Variation ofC2ORF71in Probands with Progressive Autosomal Recessive Retinal Degeneration and Controls

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

A common variant near TGFBR3 is associated with primary open angle glaucoma.

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene

Analysis of full length ADAMTS6 transcript reveals alternative splicing and a role for the 5' untranslated region in translational control.

Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retina

Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract

Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalpha.

Expression of mutant and wild-type TIMP3 in primary gingival fibroblasts from Sorsby's fundus dystrophy patients

FGF-2 release from the lens capsule by MMP-2 maintains lens epithelial cell viability.

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies

Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).

Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus).

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

TIMP3 mutation in Sorsby's fundus dystrophy: molecular insights

The spatial organization of intra-tumour heterogeneity and evolutionary trajectories of metastases in hepatocellular carcinoma