Author

Fei Yin

Central South UniversityORCID 0000-0002-7192-6308Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Chao CheniD· 1 shared Chun‐Gu Hong· 1 shared Chun‐Yuan CheniD· 1 shared Chunyu LiuiD· 1 shared Dian LuiD· 1 shared Fang LiuiD· 1 shared Fei CheniD· 1 shared Hailiang HuangiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Chao ChenORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 10, 2022

Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of MAPK3 and its contribution to variable NDD phenotypes

Fang Liu, Liang Chen, Zhengchang Li…·Xiaoli Chen

The paper identifies MAPK3 as a driver gene in 16p11.2 deletion-associated neurodevelopmental disorders, showing haplotype-specific expression and cis-regulatory enhancer SNPs contribute to variable phenotypes.

1 citation

humanbulk RNA-seq

NeurosciencebioRxivPreprintAug 26, 2021

Recurrent de novo single point mutation on the gene encoding Na+ /K+ pump results in epilepsy

Hongmin Li, Wenbao Hu, Chun‐Gu Hong…·Zhengzhao Liu

The paper identifies a de novo mutation in ATP1A2 causing epilepsy in a family and creates a mouse model to study its effects on seizures and cognitive function.

1 citation

mouseexperimental assay