Author

Xiaoli Chen

Chinese Academy of Medical Sciences & Peking Union Medical CollegeORCID 0000-0003-0536-1553Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Xiaoli Chen2 papers · University of Central Florida

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Yiping SheniD· 2 shared Zailong QiniD· 2 shared Allan Micheil InnesiD· 1 shared Ana S.A. CoheniD· 1 shared Benjamin CognéiD· 1 shared Bernt PoppiD· 1 shared Bonnie R. SullivaniD· 1 shared Boris KereniD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Yiping ShenORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 24, 2024

MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway

Maolei Gong, Jiayi Li, Yijun Liu…·Xiaoli Chen

This study identifies MARK2 variants as a cause of autism spectrum disorder by showing they disrupt the WNT/β-catenin signaling pathway and impair neural development.

DOI 10.1101/2024.04.24.24304501

humanmouse

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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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