Yiping Shen
15PUBLICATIONS
70CO-AUTHORS
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Publications (15)
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|May 01, 2023
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.Victoria Patterson, Farid Ullah, Laura Bryant
|Mar 04, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.Fang Liu, Chen Liang, Zhengchang Li
|Aug 17, 2022
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders.Xiangbin Jia, Shujie Zhang, Senwei Tan
|May 12, 2021
A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8.Sheng Yi, Yue Zhang, Zailong Qin
|Mar 16, 2021
Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.Jiasun Su, Weiliang Lu, Mengting Li
|Feb 19, 2021
A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children.Li Lin, Mengting Li, Jingsi Luo
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Frequent Collaborators
3 joint publications
Zailong Qin
2 joint publications
Jian Wang
2 joint publications
Sheng Yi
2 joint publications
Weiliang Lu
2 joint publications
Mengting Li
1 joint publications
Elizabeth Bhoj
1 joint publications
Julaiti Dilihuma
1 joint publications
Yanfei Luo
1 joint publications
Maimaiti Mireguli
1 joint publications
Fang Tang
