Lian-Hong Wu

Analysis of Large Phenotypic Variability of EEC and SHFM4 Syndromes Caused by K193E Mutation of the TP63 Gene

D. Shi, Junrui Zhang, Bin Lu, 2012, PloS one.

Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies

Guanting Lu, Liya Ma, Jin Wu, 2022, Frontiers in Molecular Neuroscience.

Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing

Guanting Lu, Lian-Hong Wu, Jian Zhang, 2021, BMC Medical Genomics.

A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicing

Yan Zhang, Guanting Lu, Xin Zhang, 2022, Frontiers in Molecular Neuroscience.

A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal Anomalies

Guanting Lu, Huiyun Xia, J. Ding, 2022, Frontiers in Genetics.