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Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 2024
KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13
Jianbo Cheng, Zhen Wang, Manpei Tang, et al.
Nucleic Acids Research
|
November 11, 2024
SV4GD: a comprehensive structural variation database specially for genetic diseases
Lei Shi, Sainan Zhang, Ying Li, et al.
Neuroscience Bulletin
|
June 24, 2025
Csde1 Mediates Neurogenesis via Post-transcriptional Regulation of the Cell Cycle
Xiangbin Jia, Wenqi Xie, Bing Du, et al.
Science Bulletin
|
April 8, 2026
Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder
Jinchen Li, Tengfei Luo, Xue Ren, et al.
The Journal of Clinical Investigation
|
August 2, 2022
GIGYF1 disruption associates with autism and impaired IGF-1R signaling
Guodong Chen, Bin Yu, Senwei Tan, et al.
Molecular Psychiatry
|
October 30, 2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
Senwei Tan, Qiumeng Zhang, Rui Zhan, et al.
Molecular Psychiatry
|
June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism
Bin Yu, Shimeng Zhu, Linhu Xiao, et al.
The Journal of Clinical Investigation
|
September 18, 2025
Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development
Xiaoxia Peng, Xiangbin Jia, Hanying Wang, et al.
Science Advances
|
August 17, 2022
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders
Xiangbin Jia, Shujie Zhang, Senwei Tan, et al.
American Journal of Human Genetics
|
November 6, 2020
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism
Hui Guo, Qiumeng Zhang, Rujia Dai, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 2024
KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13
Jianbo Cheng, Zhen Wang, Manpei Tang, et al.
Nucleic Acids Research
|
November 11, 2024
SV4GD: a comprehensive structural variation database specially for genetic diseases
Lei Shi, Sainan Zhang, Ying Li, et al.
Neuroscience Bulletin
|
June 24, 2025
Csde1 Mediates Neurogenesis via Post-transcriptional Regulation of the Cell Cycle
Xiangbin Jia, Wenqi Xie, Bing Du, et al.
Science Bulletin
|
April 8, 2026
Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder
Jinchen Li, Tengfei Luo, Xue Ren, et al.
The Journal of Clinical Investigation
|
August 2, 2022
GIGYF1 disruption associates with autism and impaired IGF-1R signaling
Guodong Chen, Bin Yu, Senwei Tan, et al.
Molecular Psychiatry
|
October 30, 2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
Senwei Tan, Qiumeng Zhang, Rui Zhan, et al.
Molecular Psychiatry
|
June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism
Bin Yu, Shimeng Zhu, Linhu Xiao, et al.
The Journal of Clinical Investigation
|
September 18, 2025
Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development
Xiaoxia Peng, Xiangbin Jia, Hanying Wang, et al.
Science Advances
|
August 17, 2022
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders
Xiangbin Jia, Shujie Zhang, Senwei Tan, et al.
American Journal of Human Genetics
|
November 6, 2020
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism
Hui Guo, Qiumeng Zhang, Rujia Dai, et al.
Page
of 3