Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome-Reference-Cited by-同舟云学术

Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome

Published:2022-11 Issue:6 Volume:9 Page:1662-1673
ISSN:2352-3042
Container-title:Genes & Diseases
language:en
Short-container-title:Genes & Diseases

Author:

Jiao Jia,Wang Li,Ni Fenfen,Wang Mo,Feng Shipin,Gao Xiaojie,Chan Han,Yang Xueying,Lee Hao,Chi Huan,Chen Xuelan,Wu Daoqi,Zhang Gaofu,Yang Baohui,Wang Anshuo,Yang Qin,Wan Junli,Yu Sijie,Li Xiaoqin,Wang Mei,Chen Xiaofeng,Mai Xianying,Ruan Xiongzhong,Yang Haiping,Li Qiu

Publisher

Elsevier BV

Subject

Cell Biology,Genetics (clinical),Molecular Biology,Biochemistry

Reference39 articles.

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3. IPNA clinical practice recommendations for the diagnosis and management of children with steroid-resistant nephrotic syndrome;Trautmann;Pediatr Nephrol,2020

4. Infants with congenital nephrotic syndrome have comparable outcomes to infants with other renal diseases;Dufek;Pediatr Nephrol,2019

5. Kidney Disease: improving Global Outcomes. Treatment of steroid-sensitive nephrotic syndrome: new guidelines from KDIGO;Lombel;Pediatr Nephrol,2013

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1. Novel mutation patterns in children with steroid-resistant nephrotic syndrome;Clinical Kidney Journal;2024-07-23

2. Nephrotic Syndrome Throughout Childhood: Diagnosing Podocytopathies From the Womb to the Dorm;Pediatric and Developmental Pathology;2024-05-14

3. Effects of a novel ANLN E841K mutation associated with SRNS on podocytes and its mechanism;Cell Communication and Signaling;2023-11-13

4. PAX2 Gene Mutation in Pediatric Renal Disorders—A Narrative Review;International Journal of Molecular Sciences;2023-08-13