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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: jiang xy. 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.
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Rao J, Liu X, Mao J, Tang X, Shen Q, Li G, Sun L, Bi Y, Wang X, Qian Y, Wu B, Wang H, Zhou W, Ma D, Zheng B, Shen Y, Chen Z, Luan J, Wang X, Wang M, Dang X, Wang Y, Wu Y, Hou L, Sun S, Li Q, Liu X, Bai H, Yang Y, Shao X, Li Y, Zheng S, Han M, Liu C, Cao G, Zhao L, Qiu S, Dong Y, Zhu Y, Wang F, Zhang D, Li Y, Zhao L, Yang C, Luo X, Chen L, Jiang X, Zhang A, Xu H; for “Internet Plus” Nephrology Alliance of National Center for Children's Care. Rao J, et al. Clin Genet. 2019 Nov;96(5):402-410. doi: 10.1111/cge.13606. Epub 2019 Jul 25. Clin Genet. 2019. PMID: 31328266
IPDN-China promotes the development of pediatric dialysis in China.
Zhai Y, Liu X, Yang Q, Dang X, Sun S, Shao X, Liu X, Wu Y, Bai H, Mao J, Dong Y, Ma Q, Kang G, Huang W, Zhu H, Fu R, Zhang A, Xu R, Sun Q, Jiang X, Lai L, Huang J, Luan J, Xia Z, Cui J, Zhao M, Wu X, Zhang Q, Li Y, Liu C, Wang M, Wang F, Tao Y, Huang Z, Zhang D, Zhao B, Chen C, Huang C, Gao X, Shen Q, Shen Y, Xu H; IPDN-China investigators. Zhai Y, et al. Pediatr Nephrol. 2020 Nov;35(11):2163-2171. doi: 10.1007/s00467-020-04630-3. Epub 2020 Jun 11. Pediatr Nephrol. 2020. PMID: 32529322
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. 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
Integrating Population Variants and Protein Structural Analysis to Improve Clinical Genetic Diagnosis and Treatment in Nephrogenic Diabetes Insipidus.
Liao P, Xiang T, Li H, Fang Y, Fang X, Zhang Z, Cao Q, Zhai Y, Chen J, Xu L, Liu J, Tang X, Liu X, Wang X, Luan J, Shen Q, Chen L, Jiang X, Ma D, Xu H, Rao J. Liao P, et al. Front Pediatr. 2021 Apr 29;9:566524. doi: 10.3389/fped.2021.566524. eCollection 2021. Front Pediatr. 2021. PMID: 33996673 Free PMC article.
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.
Liu JL, Shen Q, Wu MY, Zhu GH, Li YF, Wang XW, Tang XS, Bi YL, Gong YN, Chen J, Fang XY, Zhai YH, Wu BB, Li GM, Sun YB, Gao XJ, Liu CH, Jiang XY, Hao S, Kang YL, Gong YL, Rong LP, Li D, Wang S, Ma D, Rao J, Xu H; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Liu JL, et al. Among authors: jiang xy. World J Pediatr. 2021 Aug;17(4):409-418. doi: 10.1007/s12519-021-00428-x. Epub 2021 May 31. World J Pediatr. 2021. PMID: 34059960
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. 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.
Genetic Variations and Clinical Features of NPHS1-Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study.
Rong L, Chen L, Rao J, Shen Q, Li G, Liu J, Mao J, Feng C, Wang X, Wang S, Kuang X, Huang W, Ma Q, Liu X, Ling C, Fu R, Gao X, Ding G, Yang H, Han M, Huang Z, Li Q, Zhang Q, Lin Y, Jiang X, Xu H. Rong L, et al. Front Med (Lausanne). 2021 Nov 11;8:771227. doi: 10.3389/fmed.2021.771227. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34859019 Free PMC article.
706 results