Xiangbin Jia

机构：Ministry of Education · ORCID：0000-0001-9363-9556

发表论文 20 篇 · 总被引 472 次 · h-index 10

代表论文

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model (2018 · Molecular Autism · 被引 171)
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders (2022 · Science Advances · 被引 56)
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission (2019 · Science Advances · 被引 51)
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism (2020 · The American Journal of Human Genetics · 被引 42)
Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders (2018 · American Journal of Medical Genetics Part A · 被引 37)
GIGYF1 disruption associates with autism and impaired IGF-1R signaling (2022 · Journal of Clinical Investigation · 被引 32)