Wen-Qi Chen - Prenatal Diag Ctr, Shijiazhuang Obstet & Gynecol Hosp

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论文共 19 篇作者统计合作学者相似作者

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Analysis of a Series of 26 Cases with Prenatal Skeletal Dysplasia Via Multiplatform Genetic Detection

Li-min Cui,Hua-ying Hu, Xiao-mei Zhai, Ming-fei Qi, Yan-ming Liu, Cong-ying Han,Jing Zhang,Ming Shen, Yu-lan Xiang,Wen-qi Chen,Kai Yang,Dong-liang Zhang,Huan-xia Xing

MOLECULAR GENETICS & GENOMIC MEDICINEno. 1 (2025)

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Identification of Novel Variations in Three Cases with Rare Inherited Neuromuscular Disorder

Wen-Qi Chen, Yu-Fan Yuan, Ke-Na Hu,Dong-Lan Sun,Si-Wen Wang, Qing-Bing He, Yan-Ming Liu, Cong-Ying Han,Jing Zhang,Ya-Zhou Li

EXPERIMENTAL AND THERAPEUTIC MEDICINE（2024）

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Identification of Novel NSD1 Variations in Four Pediatric Cases with Sotos Syndrome

Zhuo Ren, Ling Yue,Hua-ying Hu, Xiao-lin Hou,Wen-qi Chen,Ya Tan,Zhe Dong,Jing Zhang

BMC MEDICAL GENOMICSno. 1 (2024)

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SGMS1 Facilitates Osteogenic Differentiation of MSCs and Strengthens Osteogenesis-Angiogenesis Coupling by Modulating Cer/PP2A/Akt Pathway

Kai Yang, Ying-yi Luan,Shan Wang,You-sheng Yan,Yi-peng Wang,Jue Wu,Yong-qing Sun,Jing Zhang,Wen-qi Chen, Yu-lan Xiang, Ze-lu Li,Dong-liang Zhang,Cheng-hong Yin

iScience（2024）

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Derivation of Induced Pluripotent Stem Cell from a Baraitser-Winter Cerebrofrontofacial Syndrome with ACTB Mutation

Xiaolin Hou, Zhaoxi Wang,Ruiyun Guo,Zijing Zhou,Jing Zhang,Yan Li, Herman Yao Akogo, Jiajia Ma,Wenqi Chen,Donglan Sun,Jun Ma,Qing Guo,Huixian Cui

STEM CELL RESEARCH（2024）

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Functional Assessment of a Novel Biallelic MYH3 Variation Causing CPSKF1B (contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome1b)

Qing-bing He, Cai-hong Wu,Dong-lan Sun,Jia-yu Yuan,Hua-ying Hu,Kai Yang,Wen-qi Chen,You-sheng Yan,Guang-yue Yin,Jing Zhang,Ya-zhou Li

Molecular Genetics & Genomic Medicine（2024）

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NTRK1 Knockdown Induces Mouse Cognitive Impairment and Hippocampal Neuronal Damage Through Mitophagy Suppression Via Inactivating the AMPK/ULK1/FUNDC1 Pathway

Kai Yang,Jue Wu,Shang Li,Shan Wang,Jing Zhang,Yi-peng Wang,You-sheng Yan,Hua-ying Hu, Ming-fang Xiong,Chao-bo Bai,Yong-qing Sun,Wen-qi Chen,Yang Zeng,Jun-liang Yuan,Cheng-hong Yin

Cell Death Discovery（2023）

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Assessment of a Novel Variation in DHODH Gene Causing Miller Syndrome: the First Report in Chinese Population

Kai Yang, Li-Man Fu,Xiao-Yang Chu,Jing Zhang,Wen-Qi Chen,You-Sheng Yan,Yi-Peng Wang,Dong-Liang Zhang,Cheng-Hong Yin,Qing Guo

MOLECULAR GENETICS & GENOMIC MEDICINE（2023）

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RBM25 Induces Trophoblast Epithelial-Mesenchymal Transition and Preeclampsia Disorder by Enhancing the Positive Feedback Loop Between Grhl2 and RBM25

Jing Zhang,Wen-qi Chen,Kai Yang, Zhao-xi Wang,Dong-lan Sun, Yuan-yuan Peng,Mei Yu,Shao-xiong Wang,Qing Guo

EXPERIMENTAL BIOLOGY AND MEDICINEno. 14 (2023): 1267-1277

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Genetic Variations in the DYNC2H1 Gene Causing SRTD3 (Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly)

Wenqi Chen,Yazhou Li,Jing Zhang, Yufan Yuan,Donglan Sun,Jiayu Yuan,Kai Yang,Ying Liang,Qing Guo

FRONTIERS IN GENETICS（2023）

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