An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome

Bony orbital maldevelopment after enucleation

(2015) Yongrong Ji et al.   JOURNAL OF ANATOMY

Long non-coding RNA ROR decoys gene-specific histone methylation to promote tumorigenesis

(2015) Jiayan Fan et al.   GENOME BIOLOGY

The combination of polyalanine expansion mutation and a novel missense substitution in transcription factor FOXL2 leads to different ovarian phenotypes in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) patients

(2012) J. Fan et al.   HUMAN REPRODUCTION

Quantitative morphometry of the orbit in Chinese adults based on a three-dimensional reconstruction method

(2010) Yongrong Ji et al.   JOURNAL OF ANATOMY

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)

(2010) J.-Y. Fan et al.   MUTAGENESIS

FOXL2 mutations in Chinese families with Blepharophimosis syndrome (BPES)

(2010) Jia-Yan Fan et al.   Translational Research