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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. Among authors: li y, li g, li q. Clin Genet. 2019 Nov;96(5):402-410. doi: 10.1111/cge.13606. Epub 2019 Jul 25. Clin Genet. 2019. PMID: 31328266
Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
Ye Q, Shen Q, Rao J, Zhang A, Zheng B, Liu X, Shen Y, Chen Z, Wu Y, Hou L, Jian S, Wei M, Ma M, Sun S, Li Q, Dang X, Wang Y, Xu H, Mao J; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of National Center for Children's Care. Ye Q, et al. Among authors: li q. Clin Genet. 2020 Mar;97(3):407-417. doi: 10.1111/cge.13663. Epub 2020 Jan 13. Clin Genet. 2020. PMID: 31674016
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: li g, li q. 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.
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