Yongjia Yang

10PUBLICATIONS
11CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Molecular evolutionAerospace structuresCancer geneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (10)

|Jul 06, 2026
Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability.

|Dec 11, 2025
Recessive SMC5 Variants in a Family with Near-Tetraploidy/Mosaic Variegated Aneuploidy.

Yongjia Yang, Nian Li, Cheng Liu

|Jul 16, 2025
AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated cases.

Cheng Liu, Fang Shen, Mei Deng

|Jun 18, 2024
Familial pancreatitis associated with a splice-site variant in CPA1.

Fang Shen, Hongmei Zhao, Mei Deng

|Dec 02, 2022
Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E.

Xiaojun Duan, Fang Shen, Yafei Deng

|Dec 25, 2021
A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis.

Fang Shen, Yongjia Yang, Pengcheng Li

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Frequent Collaborators

4 joint publications

Yu Zheng

2 joint publications

Wangming Li

2 joint publications

Liping Li

2 joint publications

Ming Tu