Jing Ma

18PUBLICATIONS
16CO-AUTHORS
Cancer geneticsNeurology and neuromuscular diseasesCancer diagnosisMolecular targetsCardiology (incl. cardiovascular diseases)
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Publications (18)

|Sep 14, 2026
Novel TCOF1 Frameshift Variant and Phenotypic Heterogeneity in a Chinese Family With Treacher Collins Syndrome.

|Jun 30, 2026
Simultaneous MT-RNR1 and MYO15A Mutations in a Family with Non-Syndromic Hearing Loss.

|Feb 04, 2026
FOXI3 establishes the ectodermal niche in pharyngeal arches for cranial neural crest cells and their lineages.

Xin Chen, Siyi Wu, Ying Chen

|May 23, 2025
FOXK2 in skeletal muscle development: a new pathogenic gene for congenital myopathy with ptosis.

Peixuan Wu, Nan Song, Yang Xiang

|Apr 16, 2025
Identification of novel TCOF1 mutations in Treacher Collins syndrome and their functional characterization.

Ying Chen, Run Yang, Xin Chen

|Jul 31, 2024
SMC3 contributes to heart development by regulating super-enhancer associated genes.

Bowen Zhang, Yongchang Zhu, Zhen Zhang

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Frequent Collaborators

2 joint publications

Lili Hao

2 joint publications

Duan Ma

2 joint publications

Ying Chen

2 joint publications

Tianyu Zhang