Vulto-van Silfhout-de Vries syndrome caused by de novo variants of DEAF1 gene: a case report and literature reviewHui Zhu, Zemin Luo, Lan Zeng et al.|Frontiers in Neurology|2023Cited by 6
Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature reviewShuyao Zhu, Ai Chen, Lan Zeng et al.|Epilepsy & Behavior|2025Cited by 2
Dual diagnosis of microcephalic osteosplastic primary dwarfism type II and benign familial infantile seizure type 2: a case reportShuyao Zhu, Lan Zeng, Xiangyou Leng et al.|Clinical Dysmorphology|2024Cited by 1
Genetic analysis of partial duplication of the long arm of chromosome 16Dan Tang, Shuyao Zhu, Jun Hui Fan et al.|BMC Medical Genomics|2024Cited by 1
Acute Necrotizing Encephalopathy Associated with SARS-CoV-2 Infection in ChildrenHui Zhu, Zemin Luo, Lan Zeng et al.|Annals of Indian Academy of Neurology|2024Cited by 1