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All papers authored by Yanqin Zhang

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2023 Yanqin Zhang

ORCID

, Xiaoyuan Wang, Jianmei Zhou, Jie Ding, Fang Wang

Abnormal mRNA Splicing Effect of COL4A3 to COL4A5 Unclassified Variants

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2022 Diana Rubel, Joseph Boulanger, Florin Craciun, Ethan Y. Xu

ORCID

, Yanqin Zhang

ORCID

, Lucy Phillips, Michelle Callahan, William Weber, Wenping Song, Nicholas Ngai, Nikolay O. Bukanov, Xingyi Shi

ORCID

, Ali Hariri, Hervé Husson

ORCID

, Oxana Ibraghimov-Beskrovnaya and 2 other authors

Anti-microRNA-21 Therapy on Top of ACE Inhibition Delays Renal Failure in Alport Syndrome Mouse Models

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2021 Xiaoyuan Wang, Yanqin Zhang

ORCID

, Jie Ding, Fang Wang

mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing

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Diana Rubel, Yanqin Zhang

ORCID

, Nenja Sowa, Rainer Girgert, Oliver Gross

ORCID

Organoprotective Effects of Spironolactone on Top of Ramipril Therapy in a Mouse Model for Alport Syndrome

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Yanqin Zhang

ORCID

, Jan Böckhaus, Fang Wang, Suxia Wang, Diana Rubel, Oliver Gross, Jie Ding

Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome

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2020 Haiyue Deng

ORCID

, Yanqin Zhang

ORCID

, Huijie Xiao, Yong Yao, Hongwen Zhang

ORCID

, Xiaoyu Liu, Baige Su, Na Guan, Xuhui Zhong, Suxia Wang, Jie Ding, Fang Wang

Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease

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Haiyue Deng, Yanqin Zhang

ORCID

, Yong Yao, Huijie Xiao, Baige Su, Ke Xu, Na Guan, Jie Ding, Fang Wang

Interpretation of Autosomal Recessive Kidney Diseases With “Presumed Homozygous” Pathogenic Variants Should Consider Technical Pitfalls

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2019 Yanqin Zhang

ORCID

, Jie Ding, Suxia Wang, Hongwen Zhang, Xuhui Zhong, Xiaoyu Liu, Ke Xu, Fang Wang

Reassessing the pathogenicity of c.2858G>T(p.(G953V)) in COL4A5 Gene: report of 19 Chinese families

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Jifan Guo, Wenping Song, Joseph Boulanger, Ethan Y. Xu, Fang Wang, Yanqin Zhang

ORCID

, Qun He, Suxia Wang, Li Yang, Cynthia Pryce, Lucy Phillips, Deidre MacKenna, Ekkehard Leberer, Oxana Ibraghimov-Beskrovnaya, Jie Ding and 1 other authors

Dysregulated Expression of microRNA-21 and Disease-Related Genes in Human Patients and in a Mouse Model of Alport Syndrome

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Haiyue Deng

ORCID

, Yanqin Zhang

ORCID

, Huijie Xiao, Yong Yao, Xiaoyu Liu, Baige Su, Hongwen Zhang, Ke Xu, Suxia Wang, Fang Wang, Jie Ding

Diverse phenotypes in children with PAX2 ‐related disorder

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Yanqin Zhang

ORCID

, Jie Ding, Hongwen Zhang, Yong Yao, Huijie Xiao, Suxia Wang, Fang Wang

Effect of heterozygous pathogenic COL4A3 or COL4A4 variants on patients with X‐linked Alport syndrome

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2018 Xiao Zhang, Yanqin Zhang

ORCID

, Yanmei Zhang, Hongbo Gu, Zhe Chen, Lei Ren, Xingxing Lu, Li Chen, Fang Wang, Yuhe Liu, Jie Ding

X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males

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Baihong Li, Yanqin Zhang

ORCID

, Fang Wang, Viji Nair, Fangrui Ding, Huijie Xiao, Yong Yao, Matthias Kretzler, Wenjun Ju

ORCID

, Jie Ding

Urinary epidermal growth factor as a prognostic marker for the progression of Alport syndrome in children

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2017 Fangrui Ding, Larysa Wickman, Su Q. Wang, Yanqin Zhang

ORCID

, Fang Wang, Farsad Afshinnia, Jeffrey Hodgin, Jie Ding, Roger C. Wiggins

Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome

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Yanqin Zhang

ORCID

, Jie Ding

Renal, auricular, and ocular outcomes of Alport syndrome and their current management

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Fang Wang, Yanqin Zhang

ORCID

, Jianhua Mao, Zihua Yu, Zhuwen Yi, Li Yu, Jun Sun, Xiuxiu Wei, Fangrui Ding, Hongwen Zhang, Huijie Xiao, Yong Yao, Weizhen Tan, Svjetlana Lovric, Jie Ding and 1 other authors

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome

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2016 Oliver Gross, Clifford E. Kashtan, Michelle N. Rheault, Judith Savige, Jeffrey H. Miner, Roser Torra, Isavella Savva, Frances Flinter, Laura Perin, Alessandra Renieri, Francesca Mari, Elisabet Ars, Constantinos Deltas, Parminder Judge, Bertrand Knebelman and 23 other authors

Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome.

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2015 Yanqin Zhang

ORCID

, Fang Wang, Jie Ding, Hongwen Zhang, Xiaoyu Liu, Suxia Wang, Huijie Xiao, Yong Yao, Jingcheng Liu, Xuhui Zhong, Na Guan, Baige Su, Guohong Wu, Lixia Yu

Long-term treatment by ACE inhibitors and angiotensin receptor blockers in children with Alport syndrome

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2014 Shu-Ping Liu, Jie Ding, Fang Wang, Yan-Qin Zhang

ORCID

, Jin-Tang Ye

Clinical characteristics and mutation analysis of three Chinese children with autosomal recessive polycystic kidney disease

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This paper was not found in any repository, but could be made available legally by the author.

2013 Yan-Qin Zhang

ORCID

, Fang Wang, Jie Ding, Hui Yan, Yan-Ling Yang

Novel OCRL mutations in Chinese children with Lowe syndrome

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