Bo Jin

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

Yun Yuan, C. Bönnemann, Chunde Li, 2021, Orphanet Journal of Rare Diseases.

Identification of a missense ARSA mutation in metachromatic leukodystrophy and its potential pathogenic mechanism

Liyuan Guo, Yidan Zhang, Jing Wang, 2019, bioRxiv.

Insulin resistance in children with primary nephrotic syndrome and normal renal function

Songming Huang, G. Ding, A. Zhang, 2012, Pediatric Nephrology.

Candida meningitis in an infant after abdominal surgery successfully treated with intrathecal and intravenous amphotericin B

F. Chen, Bo Jin, Yao Sun, 2021, Medicine.

MeQTL analysis of childhood obesity links epigenetics with a risk SNP rs17782313 near MC4R from meta-analysis

Weifeng Lu, Lingling Zhou, Weifeng Lu, 2016, Oncotarget.

Congenital muscular dystrophies in China

Zhaoxia Wang, Yun Yuan, C. Bönnemann, 2019, Clinical genetics.