1.国自然基金面上基金《UBE2O基因及其突变调控I-SMADs泛素化修饰在遗传性血色病中的致病作用及机制研究》，2021-01至2024-12，主持

2.北京市自然青年基金《SLC40A1基因 p.Y333H突变在4型遗传性血色病中的致病作用及机制研究》，2019-01至2020-12，主持

3.北京市医管中心2019年度（第五批）“青苗”计划《BMP4基因突变在遗传性血色病中的发病作用及机制研究》，2020-01至2021-12，主持

4.北京市医管中心消化内科学科协同发展中心重点项目子课题《中国遗传性血色病的临床特征、基因突变谱以及基因型-表型关系研究》，2018-01至2021-12，主持

1.国自然基金面上基金《UBE2O基因及其突变调控I-SMADs泛素化修饰在遗传性血色病中的致病作用及机制研究》，2021-01至2024-12，主持

2.北京市自然青年基金《SLC40A1基因 p.Y333H突变在4型遗传性血色病中的致病作用及机制研究》，2019-01至2020-12，主持

3.北京市医管中心2019年度（第五批）“青苗”计划《BMP4基因突变在遗传性血色病中的发病作用及机制研究》，2020-01至2021-12，主持

4.北京市医管中心消化内科学科协同发展中心重点项目子课题《中国遗传性血色病的临床特征、基因突变谱以及基因型-表型关系研究》，2018-01至2021-12，主持

1. Ouyang,Qin; Li, Yanmeng; Xu, Anjian; Zhang, Ning; Chen, Sisi; Zhou, Donghu; Zhang,Bei; Ou, Xiaojuan; Jia, Jidong; Huang, Jian*; Zhang, Wei*. Recurrent BMP4variants in exon 4 cause non-HFE-associated hemochromatosis via the BMP/SMADsignaling pathway, Orphanet J Rare Dis, 2024,19(1): 429

2. Wei Zhang#;Yanmeng Li#; Anjian Xu; Qin Ouyang; Liyan Wu; Donghu Zhou; Lina Wu; Bei Zhang; XinyanZhao; Yu Wang; Xiaoming Wang; Weijia Duan; Qianyi Wang; Hong You; Jian Huang;Xiaojuan Ou; Jidong Jia ; Identification of novel non-HFE mutations in Chinesepatients with hereditary hemochromatosis(DOI:10.1186/s13023-022-02349-y),Orphanet Journal of Rare Diseases, 2022, 17(1):216

3. LiyanWu#, Wei Zhang#, Yanmeng Li#, Donghu Zhou, Bei Zhang, Anjian Xu, Zhen Wu, LinaWu, Shuxiang Li, Xiaoming Wang, Xinyan Zhao, Qianyi Wang, Min Li, Yu Wang, JianHuang*, Xiaojuan Ou*, Jidong Jia*. Correlation of genotype and phenotype in 32patients with hereditary hemochromatosis in China. Orphanet J Rare Dis2021;16(1):398. (IF:4.123)

4. WeiZhang, Xiaoming Wang, Weijia Duan, Anjian Xu, Xinyan Zhao, Jian Huang, HongYou, Pierre Brissot, Xiaojuan Ou*, Jidong Jia*. HFE-Related Hemochromatosis ina Chinese Patient: The First Reported Case. Front Genet 2020;11:77.doi:10.3389/fgene.2020.00077. eCollection 2020. (IF:3.258)

5. Zhang W#, Xu A#, Li Y#,Zhao S, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Nan Y,You H, Jia J*, OuX*, Huang J*. A novel SLC40A1p.Y333H mutation with gain-of-function of ferroportin: a recurrent cause ofhemochromatosis in China. Liver Int 2019;39(6):1120-1127.  (IF:5.542)

6. Zhang Wei, Xinyan Zhao,Jian Huang, XiaojuanOu*, Jidong Jia*. Alagille syndrome: anuncommon cause of intrahepatic cholestasis in adults. Rev Esp Enferm Dig 2019;111(4):323-326. (IF: 1.858)

7. Li X#, Zhang W#, Zhou D#, Lv T, Xu A, Wang H,Zhao X, Zhang B, Li Y, Jia S, Wang Y, Wang X, Wu Z, Duan W, Wang Q, Nan Y,Shang J, Jiang W, Chen Y, Zheng S, Liu M, Sun L, You H, Jia J*, Ou X*, Huang J*. Complex ATP7Bmutation patterns in Wilson disease and evaluation of a yeast model forfunctional analysis of variants. Hum Mutat 2019;40(5):552-565. (IF: 4.453)

8. Lv T#, Zhang W#, Xu A#,Li Y, Zhou D, Zhang B, Li X, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Xu H,Zheng J, Zhao R, Zhu L, Dong Y, Lu L, Chen Y, Long J, Zheng S, Wang W, You H,Jia J*, Ou X*, Huang J*. Non-HFE mutations inhaemochromatosis in China: combination of heterozygous mutations involving HJVsignal peptide variants. J Med Genet 2018;55(10):650-660.(IF:5.751)

9.Zhang W#，Lv T#，Huang Jian*, Ou X*. Type4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1gene: a case report and a review of the literature. Medicine 2017；96(38):e8064.  (IF: 1.803)

10. Wei Zhang, Xiaoming Wang, Yu Wang, Xinyan Zhao,Weijia Duan, Qianyi Wang, Xiaoning Wu, Yuanyuan Kong, Hong Ma, Hong You,Xiaojuan Ou, Jidong Jia. Effective viral suppression is necessary to reducehepatocellular carcinoma development in cirrhotic patients with chronichepatitis B: Results of a 10-year follow up. Medicine 2017;96(44):e8454. (IF: 1.803)

11. 张伟; 李艳萌; 徐安健; 王晓明; 王宇; 段维佳; 赵新颜; 徐鹤祥; 姜金坪; 蒋炜; 黄坚; 欧晓娟. 中国人群2A型遗传性血色病的临床、基因突变特征及其治疗预后分析, 中 华肝脏病杂志, 2024, 32(11): 1013-1018

12.中华医学会肝病学分会. 中国遗传性血色病诊疗指南.2024,32(9):787-797. (编写专家，排名第一).

13. 张伟,赵新颜,黄坚,欧晓娟, 贾继东.威尔逊氏病的药物治疗进展.2024, 32(9):783-786.

14.张伟,黄坚,欧晓娟,贾继东.《2022年美国肝病学会实践指导:肝豆状核变性的诊断和治疗》意见要点. 2022, 38(12):2709-2711.

15.张伟,贾继东.非遗传因素对α1-抗胰蛋白酶缺乏症临床表型的影响.肝脏2019;24(11):1224-1225.

16.张伟,黄坚,欧晓娟,等.血色病国际有关p.Cys282Tyr纯合基因型血色病的治疗推荐意见.中华肝脏病杂志2019; 27(12):980-981.

17.张伟，吕婷霞，李艳萌，王晓明，赵新颜，王宇，徐安健，李潇槿，黄坚*，欧晓娟*. 3个携带HJV E3D变异的遗传性血色病家系临床表型分析.肝脏 2017, 22(7)：585-589.

18. 张伟，贾继东. 肝纤维化的发病机制及治疗新靶点. 临床肝胆病杂志2017;33(3):409-412.