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Chunjie Liu

Shanghai Jiao Tong University

5

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25

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Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family

2021 Molecular Genetics & Genomic Medicine
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Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection

2018 Pediatric Cardiology
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Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

2018 Genome Medicine
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Identification of candidate genes for congenital heart defects on proximal chromosome 8p

2016 Scientific Reports
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