Works by Chen, Yu'e

Results: 13

Application of static progressive stretch in perioperative rehabilitation nursing of patients with unicompart-mental knee arthroplasty.

Published in:

Chinese Journal of Nursing, 2024, v. 59, n. 12, p. 1462, doi. 10.3761/j.issn.0254-1769.2024.12.008

By:

CHEN Yu'e;
GAO Yuan;
KONG Dan;
GU Siqi;
KANG Shanshan;
XIE Tao

Publication type:

Article

Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-52831-9

By:

Zhuang, Jianlong;
Zhang, Na;
Chen, Yu'e;
Jiang, Yuying;
Chen, Xinying;
Chen, Wenli;
Chen, Chunnuan

Publication type:

Article

Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.964098

By:

Jianlong Zhuang;
Junyu Wang;
Qi Luo;
Shuhong Zeng;
Yu'e Chen;
Yuying Jiang;
Xinying Chen;
Yuanbai Wang;
Yingjun Xie;
Gaoxiong Wang;
Chunnuan Chen

Publication type:

Article

Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.924573

By:

Jianlong Zhuang;
Chunnuan Chen;
Yuanbai Wang;
Shuhong Zeng;
Yu'e Chen;
Yuying Jiang;
Yingjun Xie;
Gaoxiong Wang

Publication type:

Article

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.829613

By:

Zhuang, Jianlong;
Chen, Chunnuan;
Chen, Yu'e;
Zeng, Shuhong;
Jiang, Yuying;
Wang, Yuanbai;
Chen, Xinying;
Xie, Yingjun;
Wang, Gaoxiong

Publication type:

Article

Third‐generation sequencing identified two rare α‐chain variants leading to hemoglobin variants in Chinese population.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2365

By:

Zhuang, Jianlong;
Jiang, Yuying;
Chen, Yu'e;
Mao, Aiping;
Chen, Junwei;
Chen, Chunnuan

Publication type:

Article

Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis‐van Creveld syndrome.

Published in:

2023

By:

Zhuang, Jianlong;
Liu, Shufen;
Wang, Junyu;
Chen, Yu'e;
Zhang, Hegan;
Jiang, Yuying;
Wang, Gaoxiong;
Chen, Chunnuan

Publication type:

Case Study

Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 3, p. 1, doi. 10.1002/mgg3.2121

By:

Zhuang, Jianlong;
Luo, Qi;
Xie, Meihua;
Chen, Yu'e;
Jiang, Yuying;
Zeng, Shuhong;
Wang, Yuanbai;
Xie, Yingjun;
Chen, Chunnuan

Publication type:

Article

Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model.

Published in:

Molecules, 2023, v. 28, n. 14, p. 5401, doi. 10.3390/molecules28145401

By:

Lu, Xiaoyan;
Che, Qiman;
Niu, Xinkai;
Zhang, Yilin;
Chen, Yu'e;
Han, Qing;
Li, Miaoqing;
Wang, Shuang;
Lan, Jihong

Publication type:

Article

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study.

Published in:

2024

By:

Zhuang, Jianlong;
Zhang, Na;
Fu, Wanyu;
Jiang, Yuying;
Chen, Yu'e;
Chen, Chunnuan

Publication type:

Case Study

Prenatal diagnosis and molecular cytogenetic analysis of pure chromosome 10p15.3 microdeletion using chromosomal microarray analysis.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-02063-7

By:

Zhang, Na;
Huang, Nan;
Chen, Yu'e;
Chen, Xinying;
Zhuang, Jianlong

Publication type:

Article

Case Report: Prenatal diagnosis of novel compound heterozygous variants in WDR35 gene causing short-rib thoracic dysplasia 7 with or without polydactyly.

Published in:

Frontiers in Pediatrics, 2025, p. 1, doi. 10.3389/fped.2024.1503455

By:

Zhuang, Jianlong;
Wang, Junyu;
Huang, Zhengping;
Chen, Yu'e;
Chen, Chunnuan

Publication type:

Article

Molecular characterization of a rare TP63 variant associated with split-hand/split-foot malformation 4 and incomplete penetrance: disruption of the p63-Dlx signaling pathway.

Published in:

BMC Genomics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s12864-025-11297-3

By:

Zhuang, Jianlong;
Li, Yanqing;
Chen, Yu'e;
Zhang, Hegan;
Liu, Shufen;
Hu, Manman;
Chen, Chunnuan

Publication type:

Article