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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: gao x. 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.
Multi-centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children.
Shen Q, Chen J, Yu M, Lin Z, Nan X, Dong B, Fang X, Chen J, Ding G, Zhang A, Gao C, Miao L, Xu Y, Jiang X, Bai H, Zhuang J, Gao X, Xu H; for Chinese Children Genetic Kidney Disease Database (CCGKDD). Shen Q, et al. Among authors: gao c, gao x. Clin Genet. 2021 Apr;99(4):558-564. doi: 10.1111/cge.13913. Epub 2021 Feb 2. Clin Genet. 2021. PMID: 33382082
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. 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
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. Among authors: gao x. 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.
Psychological research of the children with chronic kidney disease and their guardians during the COVID-19 pandemic.
Xiong HY, Zhang G, Wang L, Li Z, Shen Q, Li Y, Zhu H, Du Y, Sun L, Zhao B, Zhao L, Fu H, Li X, Gao X, Hao S, Ding J, Chen Z, Xu Z, Liu X, Tao Y, Zhang A, Li Q, Wang M. Xiong HY, et al. Among authors: gao x. Front Public Health. 2022 Oct 17;10:922678. doi: 10.3389/fpubh.2022.922678. eCollection 2022. Front Public Health. 2022. PMID: 36324445 Free PMC article.
A genomic association study revealing subphenotypes of childhood steroid-sensitive nephrotic syndrome in a larger genomic sequencing cohort.
Chan H, Ni F, Zhao B, Jiang H, Ding J, Wang L, Wang X, Cui J, Feng S, Gao X, Yang X, Chi H, Lee H, Chen X, Li X, Jiao J, Wu D, Zhang G, Wang M, Cun Y, Ruan X, Yang H, Li Q. Chan H, et al. Among authors: gao x. Genes Dis. 2023 Sep 27;11(4):101126. doi: 10.1016/j.gendis.2023.101126. eCollection 2024 Jul. Genes Dis. 2023. PMID: 38560502 Free PMC article.
Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome.
Jiao J, Wang L, Ni F, Wang M, Feng S, Gao X, Chan H, Yang X, Lee H, Chi H, Chen X, Wu D, Zhang G, Yang B, Wang A, Yang Q, Wan J, Yu S, Li X, Wang M, Chen X, Mai X, Ruan X, Yang H, Li Q. Jiao J, et al. Among authors: gao x. Genes Dis. 2022 May 5;9(6):1662-1673. doi: 10.1016/j.gendis.2022.03.023. eCollection 2022 Nov. Genes Dis. 2022. PMID: 36157477 Free PMC article.
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