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Jing Zhang

7PUBLICATIONS

5CO-AUTHORS

CybercrimeDevelopmental genetics (incl. sex determination)Medical genetics (excl. cancer genetics)MechanobiologyGene expression (incl. microarray and other genome-wide approaches)

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Publications (7)

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|May 15, 2025

SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.

Jing Zhang, Kai Yang, Wen-Qi Chen

|Jan 20, 2025

Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection.

Li-Min Cui, Hua-Ying Hu, Xiao-Mei Zhai

|Mar 06, 2024

Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).

Qing-Bing He, Cai-Hong Wu, Dong-Lan Sun

|Sep 20, 2023

RBM25 induces trophoblast epithelial-mesenchymal transition and preeclampsia disorder by enhancing the positive feedback loop between Grhl2 and RBM25.

Jing Zhang, Wen-Qi Chen, Kai Yang

|Jun 07, 2023

Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation.

Xiaohui Wen, Huanxia Xing, Keyan Qi

|Apr 30, 2023

Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.

Kai Yang, Li-Man Fu, Xiao-Yang Chu

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Frequent Collaborators

3 joint publications

Kai Yang

2 joint publications

Wen-Qi Chen

2 joint publications

Huanxia Xing

2 joint publications

Hua-Ying Hu

1 joint publications

Hong Qi

Frequent Collaborators

3 joint publications

Kai Yang

2 joint publications

Wen-Qi Chen

2 joint publications

Huanxia Xing

2 joint publications

Hua-Ying Hu

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