Panfeng Wang

Bone Morphogenetic Protein (BMP) signaling in development and human diseases

BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome

Merkel Cells Activate Sensory Neural Pathways through Adrenergic Synapses

Myopia

Updates of pathologic myopia

Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

The epidemics of myopia: Aetiology and prevention

Myopia genetics: a review of current research and emerging trends

Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer

Extracellular matrix structure

The GEnes in Myopia (GEM) study in understanding the aetiology of refractive errors

Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies

The Fibroblast Growth Factor signaling pathway

The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease

A Functional Polymorphism at the FGF10 Gene Is Associated With Extreme Myopia

The regulatory roles of small leucine‐rich proteoglycans in extracellular matrix assembly

Common variants in chromosome 4q25 are associated with myopia in Chinese adults

Novel SOX2 Mutation Associated With Ocular Coloboma in a Chinese Family

High Myopia Is Not Associated with the SNPs in theTGIF, Lumican,TGFB1, andHGFGenes

An evaluation of OPTC and EPYC as candidate genes for high myopia.

Replication Study SupportsCTNND2as a Susceptibility Gene for High Myopia

Sequence variations of GRM6 in patients with high myopia.

Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma.