邢清和

博士,研究员,博士生导师
地址:东安路 131号,科研2号楼A2-009室,上海 200032
电话:021-54237615(办公室)
传真:021-54237615
邮箱:qhxing@fudan.edu.cn
1. Cheng Y, Li ZD, Guan ZH, Wang L, Qiu YL, Fang WY, Zhao J, Zhang K, Li JQ, Xing QH*, Wang JS*. Liver transcriptome sequencing contributes to the molecular diagnosis of genetic liver diseases. Hepatology. 2026 Mar 19. doi: 10.1097/HEP.0000000000001747.
2. Ding J, She HY, Cheng Y, Sun HY, Feng JY, Liu T, Qiu YL, Wei BX, Zhang J, Su Y, Li YQ, Zhang JJ, Chen SY, Wang T, Yu Y, van IJzendoorn SCD*, Wang JS*, Xing QH*. A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasis. Hepatology. 2025 Aug 19. doi: 10.1097/HEP.0000000000001501.
3. Qiao Y, Lv N, Li T, Cheng Y, Li Y, Dong J, Han M, Gu Y, Shang Q*, Xing Q*. Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study. Genes Dis. 2024 Aug 9;12(4):101389.
4. Wang Y, Xu Y, Zhou C, Cheng Y, Qiao N, Shang Q, Xia L, Song J, Gao C, Qiao Y, Zhang X, Li M, Ma C, Fan Y, Peng X, Wu S, Lv N, Li B, Sun Y, Zhang B, Li T, Li H, Zhang J, Su Y, Li Q, Yuan J, Liu L, Moreno-De-Luca A, MacLennan AH, Gecz J, Zhu D, Wang X, Zhu C*, Xing Q*. Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy. Nat Med. 2024 May;30(5):1395-1405.
5. Cheng Y; Xu Y; Li H; Qiao Y; Wang Y; Su Y; Zhang J; Wang X; Song L; Ding J; Wang D; Zhu C*; Xing Q*. Genetic variants in the HLA region contribute to the risk of cerebral palsy. Biochim Biophys Acta Mol Basis Dis. 2023 Dec 30;1870(3):167008.
6. Zhang J, Zhang Y, Shang Q, Cheng Y, Su Y, Zhang J, Wang T, Ding J, Li Y, Xie Y*, Xing Q*. Gain-of-Function KIDINS220 Variants Disrupt Neuronal Development and Cause Cerebral Palsy. Movement Disorders. Mov Disord. 2024 Mar;39(3):498-509.
7. Jiang M, Yang J, Yang L, Wang L, Wang Ting, Han S, Cheng Ye, Chen Z, Su Y, Zhang L, Yang F, Chen S, Zhang J, Xiong Hao, Wang L, Zhang Z, Ma L, Luo X*, and Xing Q*. An association study of HLA with levofloxacin-induced severe cutaneous adverse drug reactions in Han Chinese. iScience. 2023, Aug 18; 26(8): 107391.
8. Qiu YL, Wang L, Huang M, Lian M, Wang F, Gong Y, Ma X, Hao CZ, Zhang J, Li ZD, Xing* QH, Cao M*, Wang JS*. Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis. J Cell Physiol. 2022 Jun;237(6):2713-2723.
9. Jiang M, Yang F, Zhang L, Xu D, Jia Y, Cheng Y, Han S, Wang T, Chen Z, Su Y, Zhu Z, Chen S, Zhang J, Wang L, Yang L, Yang J, Luo X*, Xing Q*. Unique motif shared by HLA-B*59:01 and HLA-B*55:02 is associated with methazolamide-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese. J Eur Acad Dermatol Venereol. 2022 Jun;36(6):873-880.
10. Wang Y, Qiao Y, Cheng Y, Su Y, Song L, Xu Y, Li H, Zhang L, Song J, Zhang X, Wang J, Zhu D, Tang T, Shang Q, Gao C, Wang X, Zhu C*, Xing Q*. TEP1 is a risk gene for sporadic cerebral palsy.J Genet Genomics. 2021 Dec;48(12):1134-1138.
11. Liu J, Mayekar MK, Wu W, Yan M, Guan H, Wang J, Zaman A, Cui Y, Bivona TG, Choudhry H, Xing Q*, Cao W*. Long non-coding RNA ESCCAL-1 promotes esophageal squamous cell carcinoma by down regulating the negative regulator of APOBEC3G. Cancer Lett. 2020 Nov 28;493:217-227.
12. Xiong H, Jiang M, Shao F, Ye H, Zhang W, Chen Z, Zeng F, Chen SA, Yuan H, Yan L, Xing Q, Luo X. Risk and Association of HLA Alleles with Methimazole-Induced Cutaneous Adverse Reactions in Chinese Han Population. J Invest Dermatol. 2021 Feb;141(2):437-440.
13. Qi Z, Li S, Su Y, Zhang J, Kang Y, Huang Y, Jin F, Xing Q*. Role of microRNA-145 in protection against myocardial ischemia/reperfusion injury in mice by regulating expression of GZMK with the treatment of sevoflurane. J Cell Physiol. 2019 Sep;234(9):16526-16539.
14. Wang J, Tian GG, Zheng Z, Li B, Xing Q*, Wu J*. Comprehensive Transcriptomic Analysis of Mouse Gonadal Development Involving Sexual Differentiation, Meiosis and Gametogenesis. Biol Proced Online. 2019;21:20.
15. Zhou D, Wei Z, Kuang Z, Luo H, Ma J, Zeng X, Wang K, Liu B, Gong F, Wang J, Lei S, Wang D, Zeng J, Wang T, He Y, Yuan Y, Dai H, He L*, Xing Q*. A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation. J Cell Mol Med. 2017 Apr;21(4):802-815.
16. Qiu YL, Gong JY, Feng JY, Wang RX, Han J, Liu T, Lu Y, Li LT, Zhang MH, Sheps JA, Wang NL, Yan YY, Li JQ, Chen L, Borchers CH, Sipos B, Knisely AS, Ling V*, Xing QH*, Wang JS*. Defects in MYO5B are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis. Hepatology. 2017;65(5):1655-1669
17. Bi D, Chen M, Zhang X, Wang H, Xia L, Shang Q, Li T, Zhu D, Blomgren K, He L, Wang X, Xing Q*, Zhu C*. The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy. J Neuroinflammation. 2014 Jun 6;11(1):100.
18. Zhang JY, Chen XD, Zhang Z, Wang HL, Guo L, Liu Y, Zhao XZ, Cao W*, Xing QH*, Shao FM. The adenosine deaminase acting on RNA 1 p150 isoform is involved in the pathogenesis of dyschromatosis symmetrica hereditaria. Br J Dermatol. 2013;169(3):637-44.