Kun Xia

23PUBLICATIONS
124CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Optical technologyMolecular evolutionPredictive and prognostic markers
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Publications (23)

|Jun 17, 2026
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder.

|Jun 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism.

|Feb 27, 2026
P4HA2 Participates in Pathogenesis of Refractive Error by Regulating Collagen Posttranslational Modification and Extracellular Matrix Balance.

Yanling Liu, Shanshan Dong, Furong Huang

|Sep 30, 2025
Gene4Denovo2: an updated platform for human de novo mutations discovery and interpretation.

Zhaopo Zhu, Pei Yu, Xinxin Mao

|Nov 23, 2024
GoFCards: an integrated database and analytic platform for gain of function variants in humans.

Wenjing Zhao, Youfu Tao, Jiayi Xiong

|Oct 30, 2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay.

Senwei Tan, Qiumeng Zhang, Rui Zhan

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Frequent Collaborators

9 joint publications

Hui Guo

6 joint publications

Beisha Tang

5 joint publications

Evan E Eichler

4 joint publications

Jinchen Li