Qi Tian

5PUBLICATIONS
20CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyGene mappingOptical technologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

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

|Aug 28, 2025
Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay.

Liyu Zang, Yaoling Han, Qiumeng Zhang

|Dec 11, 2023
Exome sequencing-aided precise diagnosis of four families with type I Stickler syndrome.

Runyi Tian, Ping Tong, Yuhong He

|Oct 18, 2023
CCDC66 mutations are associated with high myopia through affected cell mitosis.

Xiaozhen Chen, Ping Tong, Ying Jiang

|Apr 09, 2022
GLRA2 gene mutations cause high myopia in humans and mice.

Qi Tian, Ping Tong, Gong Chen

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Frequent Collaborators

2 joint publications

Zhengmao Hu

1 joint publications

Lu Xia

1 joint publications

Hailiang Guo

1 joint publications

Ruiting Liu