1. Liang F, Wang B, Geng J, You G, Fa J, Zhang M, Sun H, Chen H, Fu Q, Zhang X （共同通讯作者）, Zhang Z. SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome. Elife, 2021 ;10:e67481.
2. Jiang H, Cheng H, Cao Q, Fei A, Yuan M, Zhang L, Fei S, Li J, Yang S, Wu J, Fu Q, Li S, Zhang X. （通讯作者） Clinical features, laboratory findings and persistence of virus in 10 children with coronavirus disease 2019 (COVID-19). Biomed J, 2021;44(1):94-100.
3. Fa J, Zhang X （共同第一作者）, Zhang X, Qi M, Zhang X, Fu Q, Xu Z, Gao Y, Wang B. Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB. Front Cell Dev Biol,2021;9:660576.
4. Zhang X, Wang B, You G, Xiang Y, Fu Q, Yu Y, Zhang X. （通讯作者） Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle. BMC Med Genomics,2021;14(1):243.
5. Zu B, Zhang X （共同第一作者）, Xu Y, Xiang Y, Wang Z, Cai H, Wang B, You G, Fu Q. Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing. Comput Struct Biotechnol J ,2021 ;19:3482-3490
6. Xiang Y, Li X, Zhan Z, Feng J, Cai H, Li Y, Fu Q, Xu Y, Jiang H, Zhang X. （通讯作者） A Novel Nonsense GLI3 Variant Is Associated With Polydactyly and Syndactyly in a Family by Blocking the Sonic Hedgehog Signaling Pathway. Front Genet,2020;11:542004
7. Zhang X, Wang B, Zhang L, You G, Palais RA, Zhou L, Fu Q. Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting. BMC Genomics,2018;19(1):485.
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