Author

Dian Lu

Third Affiliated Hospital of Guangzhou Medical UniversityORCID 0000-0003-4920-6424Unclaimed ORCID profile · follow to get notified of new preprints

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Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Chao CheniD· 1 shared Chunyu LiuiD· 1 shared Fang LiuiD· 1 shared Fei CheniD· 1 shared Fei YiniD· 1 shared Hailiang HuangiD· 1 shared Haiming YuaniD· 1 shared Hongying WangiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Chao ChenORCID

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1 paper

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

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