Bo Zhang

Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy: A Systematic Review and Meta-analysis.

M. Sahin, A. Poduri, Sara A. Lewis, 2022, JAMA neurology.

16p13.11 deletion variants associated with neuropsychiatric disorders cause morphological and synaptic changes in induced pluripotent stem cell-derived neurons

C. Brownstein, N. Makhortova, K. Winden, 2022, Frontiers in Psychiatry.

Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability.

Baiyun Chen, Yao-dong Zhang, Jinghui Kong, 2022, European journal of medical genetics.

H19 suppresses the growth of hepatoblastoma cells by promoting their apoptosis via the signaling pathways of miR‐675/FADD and miR‐138/PTK2

Lili Ge, Jinghui Kong, Yinsen Song, 2018, Journal of cellular biochemistry.

Clinical Features, Diagnosis and Treatment of Children's Wernicke’s Encephalopathy

Lili Ge, Chongfen Chen, Shuying Luo, 2018 .

[Clinical and genetic study of a child with delayed language development carrying ring 22 and a 22q13 microdeletion].

Lili Ge, Jinghui Kong, Yinsen Song, 2020, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Gastrodin Rescues Autistic-Like Phenotypes in Valproic Acid-Induced Animal Model

Jing Tao, B. Zhang, Yidan Qiao, 2018, Front. Neurol..