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Erge Zhang

Shanghai Jiao Tong University

8

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31

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MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation.

2020 Journal of Molecular Medicine
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Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect

2019 Frontiers in Genetics
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A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

2018 Journal of Translational Medicine
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JAG1 loss‑of‑function mutations contributed to Alagille syndrome in two Chinese families

2018 Molecular Medicine Reports
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A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

2017 Scientific Reports
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