Xiangbin Jia - Concepedia

Author

Xiangbin Jia

Central South University ORCID

Also Known As

Jia, Xiangbin, Xiangbin Jia

Publications

432

Citations

H-Index

Concepts

All Affiliations

Central South University Chinese Academy of Sciences Center for Excellence in Brain Science and Intelligence Technology Howard Hughes Medical Institute University of Washington

About

Xiangbin Jia is an author at Central South University specializing in social sciences, developmental biology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	111
2	Social Sciences	4	4	111
3	Neuroscience	4	4	111
4	Autism	3	3	95
5	Cell Biology	1	1	16

Xiangbin Jia

Publications

370

Citations

H-Index

Page 1

	Year	Citations
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model Hui Guo, Tianyun Wang, Huidan Wu, Molecular Autism	2018	165
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders Xiangbin Jia, S. Zhang, Senwei Tan, Science Advances	2022	49
Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission Hui Guo, Ying Li, Lu Shen, Science Advances	2019	45
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism Hui Guo, Qiumeng Zhang, Rujia Dai, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologySyndromic AutismGeneticsCore Features	2020	38
Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development Wenjing Zhao, Jieqiong Tan, Tengfei Zhu, Journal of genetics and genomics/Journal of Genetics and Genomics Down SyndromeNeurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologyBrain Development	2019	29
GIGYF1 disruption associates with autism and impaired IGF-1R signaling Guodong Chen, Bin Yu, Senwei Tan, Journal of Clinical Investigation Brain DevelopmentGeneticsDisease Gene IdentificationSocial SciencesAutism Spectrum Disorder	2022	28
Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis Guodong Chen, Lin Han, Senwei Tan, Journal of genetics and genomics/Journal of Genetics and Genomics Impairs Neuronal DevelopmentNeuroregenerationDevelopmental BiologyBrain DevelopmentNeurodevelopment	2022	16

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