Si Chen

Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification

Zhidong Cen, You Chen, Si Chen et al. · Brain · 2019 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Protease-Activable Cell-Penetrating Peptide–Protoporphyrin Conjugate for Targeted Photodynamic Therapy in Vivo

Shiying Li, Hong Cheng, Wen‐Xiu Qiu et al. · ACS Applied Materials & Interfaces · 2015 · 91 citations

Pharmacy, Pharmaceutics, Pharmacology +17

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens

Hongjun Li, Hongjun Li, Qiaolian Wen et al. · Journal of Cystic Fibrosis · 2012 · 40 citations

Life Sciences, Genetics, Molecular Genetics +14

Loss of E-cadherin is causal to pathologic changes in chronic lung disease

Baishakhi Ghosh, Jeffrey Loube, Shreeti Thapa et al. · Communications Biology · 2022 · 40 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China

Si Chen, Zhidong Cen, Feng Fu et al. · Parkinsonism & Related Disorders · 2019 · 37 citations

Life Sciences, Genetics, Neurology +17