Lu Shen

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

Hui Guo, Tianyun Wang, Huidan Wu et al. · Molecular Autism · 2018 · 165 citations · Full text

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort

Hui Guo, Peng Yu, Zhengmao Hu et al. · Scientific Reports · 2017 · 73 citations · Full text

Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission

Hui Guo, Ying Li, Lu Shen et al. · Science Advances · 2019 · 45 citations · Full text

Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development

Wenjing Zhao, Jieqiong Tan, Tengfei Zhu et al. · Journal of genetics and genomics/Journal of Genetics and Genomics · 2019 · 29 citations

Down Syndrome, Neurodevelopmental Disorders, Developmental Anomaly +14

Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy

Ashfaque Ahmed, Meng Wang, Gaber Bergant et al. · Human Genetics · 2020 · 29 citations

Neurological Disorder, Neuroanatomy, Genetics +9