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Jianjun Chen

6PUBLICATIONS
0CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Liquid biopsiesGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (6)

Sort by Publication Date:
|Feb 13, 2025
A novel KDM5C mutation associated with intellectual disability: molecular mechanisms and clinical implications.

Yunlong Meng, Xinyao Wang, Kangyu Liu

|Nov 07, 2022
FYCO1 regulates migration, invasion, and invadopodia formation in HeLa cells through CDC42/N-WASP/Arp2/3 signaling pathway.

Xuejiao Sun, Linlin Zhou, Xinyao Wang

|Aug 18, 2022
Identification and functional analysis of two GJA8 variants in Chinese families with eye anomalies.

Linlin Zhou, Xuejiao Sun, Xinyao Wang

|Nov 06, 2021
Identification and functional study of FOXC1 variants in Chinese families with glaucoma.

Xinyao Wang, Xiangyuan Liu, Yuying Li

|May 31, 2021
A novel BLOC1S5-related HPS-11 patient and zebrafish with bloc1s5 disruption.

Zilin Zhong, Zhuanbin Wu, Jun Zhang

|Feb 26, 2020
Mutation screening of the USH2A gene reveals two novel pathogenic variants in Chinese patients causing simplex usher syndrome 2.

Chenhao He, Xinyu Liu, Zilin Zhong

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