Chunli Wang - Nanjing Key Laboratory of Pediatrics Children's Hospital, Nanjing Medical University

基本信息

浏览量：12

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 45 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Functional Analysis of Heterozygous Variants in the SALL1 Gene in 2 Children with Townes-Brocks Syndrome with FSGS

Rong Liang,Bixia Zheng,Chunli Wang,Sanlong Zhao, Wei Zhou,Ying Chen,Ruochen Che

BMC Pediatricsno. 1 (2025): 1-9

引用0浏览0WOS引用

Generation of an Ipsc Line (Dpnjmui002-A) from a Progressive Familial Intrahepatic Cholestasis 3 (PFIC3) Patient with a Heterozygous Mutation in the ABCB4 Gene

Kangkang Wu,Chunli Wang, Huiyi Hu, Ying Shen,Yucan Zheng,Guorui Hu,Zhifeng Liu

Stem cell research (2025): 103745-103745

引用0浏览0WOS引用

A Comprehensive Splicing Characterization of COL4A5 Mutations and Prognostic Significance in a Single Cohort with X-linked Alport Syndrome

Haomiao Li, Shengnan Zhang,Wei Zhou,Chunli Wang,Chunhua Zhu,Sanlong Zhao,Fei Zhao,Zhanjun Jia,Aihua Zhang,Bixia Zheng,Guixia Ding

Frontiers in genetics (2025): 1564343-1564343

引用0浏览0WOS引用

Whole-exome Sequencing Identifies Novel Truncating ALPK3 Variants in a Compound Heterozygous State Associated with Pediatric Hypertrophic Cardiomyopathy and Phenotypic Heterogeneity

Yuqi Wang, Ziwei Wang, Ningning Sun, Jie Yin, Yi Chen,Chunli Wang,Shiwei Yang

Gene (2025): 149597-149597

引用0浏览0WOS引用

Generation of Human Induced Pluripotent Stem Cell Lines Derived from a Patient Carrying an Intragenic Deletion in the NFIA Gene

Ning Zhou, Shengnan Zhang,Chunli Wang,Bixia Zheng,Aihua Zhang,Wei Zhou

Human Cellno. 3 (2025): 1-7

引用0浏览0WOS引用

Severe Conduction Block and Cardiomyopathy Associated with Desminopathy

Ningning Sun,Chunli Wang,Shiwei Yang

Cardiology in the youngno. 4 (2025): 850-852

引用0浏览0WOS引用

Genetic Insights into Craniosynostosis: Identification of Novel IL11RA Variants in Chinese Pediatric Patients

Ziwei Liu, Ding Zhou,Chunli Wang,Bixia Zheng,Qing Yan,Wei Zhou,Gang Wang

Molecular genetics & genomic medicineno. 5 (2025): e70106-e70106

引用0浏览0WOS引用

A Rare Homozygous Mutation in the YARS2 Gene Presents with Hypertrophic Cardiomyopathy, Lactic Acidosis and Anemia in a Chinese Infant

Dandan Xiang,Kangkang Xu, Mei Chen,Zhongman Zhang, Ningning Sun, Yuying Qi, Jie Lu,Chunli Wang,Shiwei Yang

GENE (2024)

引用0浏览0WOS引用

Compound Heterozygous Variants of ANKFY1 in a Child with Infantile-Onset Proteinuria and Movement Disorder

Luyan Zhang,Xueqin Cheng,Chunli Wang,Wei Zhou,Bixia Zheng,Aihua Zhang

Clinical Kidney Journalno. 6 (2024)

引用0浏览0WOS引用

Treatment Strategy for Heart Failure Complicated with Complete Left Bundle Branch Block and Atrial Tachycardia: a Case Report

Jian Wang,Qing-Qing Zhang,Jie Lin, Wei Yuan,Li-Chun Wang,Yu-Cheng Wu

Journal of Medical Case Reportsno. 1 (2024)

引用0浏览0WOS引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn