Liang Ma

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 678 citations

Sclerostin, Developmental Biology, Genetic Disorder +6

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

Liang Ma · Human Molecular Genetics · 1996 · 173 citations

Melatonin attenuates MPTP-induced neurotoxicity via preventing CDK5-mediated autophagy and SNCA/α-synuclein aggregation

Ling‐Yan Su, Hao Li, Li Lv et al. · Autophagy · 2015 · 125 citations · Full text

Mptp Injection, Cell Death, Synaptic Signaling +19

Draft genome of the Chinese mitten crab, <i>Eriocheir sinensis</i>

Linsheng Song, Chao Bian, Yongju Luo et al. · GigaScience · 2016 · 112 citations · Full text

Divergent neuronal DNA methylation patterns across human cortical development reveal critical periods and a unique role of CpH methylation

Amanda J. Price, Leonardo Collado‐Torres, Nikolay A. Ivanov et al. · Genome biology · 2019 · 91 citations · Full text