Fei Yi

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1.

Marius Wernig, T. Südhof, Marius Wernig, 2015, Cell stem cell.

Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons

Thomas C. Südhof, Marius Wernig, T. Südhof, 2016, Science.

Analysis of conditional heterozygous STXBP1 mutations in human neurons.

T. Südhof, Marius Wernig, Yan Han, 2015, The Journal of clinical investigation.

LncRNA ITSN1-2 knockdown inhibits OGD/R-induced inflammation and apoptosis in mouse hippocampal neurons via sponging miR-195-5p

Fei Yi, Fei Zhu, Jianzhong Xiong, 2021, Neuroreport.