Guo, Hui

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

Guo, H., Wang, T., Wu, H., Long, M., Coe, B. P., Li, H., Xun, G., Ou, J., Chen, B., Duan, G., et al. (2018) · Molecular Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 154

Novel West syndrome candidate genes in a Chinese cohort

Peng, J., Wang, Y., He, F., Chen, C., Wu, L., Yang, L., Ma, Y., Zhang, W., Shi, Z., Chen, C., et al. (2018) · CNS Neuroscience & Therapeutics

Epilepsy research and treatmentGenomics and Rare Diseases

Cited by 86

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

Guo, H., Peng, Y., Hu, Z., Li, Y., Xun, G., Ou, J., Sun, L., Xiong, Z., Liu, Y., Wang, T., et al. (2017) · Scientific Reports

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 71

ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model

Vitobello, A., Mazel, B., Lelianova, V. G., Zangrandi, A., Petitto, E., Suckling, J., Salpietro, V., Meyer, R., Elbracht, M., Kurth, I., et al. (2022) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 46

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism

Guo, H., Zhang, Q., Dai, R., Yu, B., Hoekzema, K., Tan, J., Tan, S., Jia, X., Chung, W. K., Hernan, R., et al. (2020) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 38