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Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.
Yang X, Li Y, Fang Y, Shi H, Xiang T, Liu J, Liu J, Tang X, Fang X, Chen J, Zhai Y, Shen Q, Bi Y, Qian Y, Wu B, Wang H, Zhou W, Ma D, Bai H, Mao J, Chen L, Wang X, Gao X, Zhang R, Zhuang J, Zhang A, Jiang X, Xu H, Rao J. Yang X, et al. Among authors: liu j. BMC Med Genomics. 2021 Oct 25;14(1):250. doi: 10.1186/s12920-021-01102-x. BMC Med Genomics. 2021. PMID: 34696790 Free PMC article.
Multidisciplinary approach to screening and management of children with Fabry disease: practice at a Tertiary Children's Hospital in China.
Shen Q, Liu J, Chen J, Zhou S, Wang Y, Yu L, Sun L, Wang L, Wu B, Liu F, Cao Y, Huang Y, Wang J, Yang C, Zhu D, Ma Y, Xu Z, Lu W, Fu L, Zhou W, Xu H. Shen Q, et al. Among authors: liu j, liu f. Orphanet J Rare Dis. 2021 Dec 14;16(1):509. doi: 10.1186/s13023-021-02136-1. Orphanet J Rare Dis. 2021. PMID: 34906154 Free PMC article.
Comparative proteomic analysis of children FSGS FFPE tissues.
Ni J, Tian S, Bai L, Lv Q, Liu J, Liu J, Fang Y, Zhai Y, Shen Q, Rao J, Ding C, Xu H. Ni J, et al. Among authors: liu j. BMC Pediatr. 2022 Dec 12;22(1):707. doi: 10.1186/s12887-022-03764-7. BMC Pediatr. 2022. PMID: 36503536 Free PMC article.
COQ8B nephropathy: Early detection and optimal treatment.
Song X, Fang X, Tang X, Cao Q, Zhai Y, Chen J, Liu J, Zhang Z, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Liu C, Shen Q, Xu H, Rao J. Song X, et al. Among authors: liu j, liu c. Mol Genet Genomic Med. 2020 Aug;8(8):e1360. doi: 10.1002/mgg3.1360. Epub 2020 Jun 16. Mol Genet Genomic Med. 2020. PMID: 32543055 Free PMC article.
Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
Sun S, Xu L, Bi Y, Wang J, Zhang Z, Tang X, Cao Q, Zhai Y, Chen J, Fang X, Liu J, Fang Y, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Shen J, Dong K, Liu X, Zheng B, Zhang A, Wang X, Wu Y, Ma D, Shen Q, Rao J, Xu H. Sun S, et al. Among authors: liu j, liu x. Eur J Med Genet. 2020 Nov;63(11):104047. doi: 10.1016/j.ejmg.2020.104047. Epub 2020 Sep 4. Eur J Med Genet. 2020. PMID: 32891756 Free article.
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.
Tang X, Liu C, Liu X, Chen J, Fan X, Liu J, Ma D, Cao G, Chen Z, Xu D, Zhu Y, Jiang X, Cheng L, Wu Y, Hou L, Li Y, Shao X, Zheng S, Zhang A, Zheng B, Jian S, Rong Z, Su Q, Gao X, Rao J, Shen Q, Xu H; Chinese Children Genetic Kidney Disease Database (CCGKDD); “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Tang X, et al. Among authors: liu j, liu x, liu c. J Med Genet. 2022 Feb;59(2):147-154. doi: 10.1136/jmedgenet-2020-107184. Epub 2020 Dec 15. J Med Genet. 2022. PMID: 33323469
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study.
Liu JL, Wang XW, Liu CH, Gao DMX, Jiang XY, Mao JH, Zhu GH, Zhang AH, Wang M, Dang XQ, Zhuang JQ, Li YF, Bai HT, Zhang RF, Shen T, Bi YL, Sun YB, Wang X, Wu BB, Chen J, Rao J, Tang XS, Shen Q, Xu H; Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of the National Center for Children's Care Department of Nephrology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China. Liu JL, et al. Among authors: liu ch. Nephrol Dial Transplant. 2022 Dec 22;38(9):1981-91. doi: 10.1093/ndt/gfac338. Online ahead of print. Nephrol Dial Transplant. 2022. PMID: 36549658 Free PMC article.
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