日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Neonatal seizures associated with a rare familial 16p11.2 microduplication: A case report

一例罕见家族性16p11.2微重复相关的新生儿癫痫病例报告

期刊:Journal of International Medical Research
影响因子:1.5
doi:10.1177/03000605251358613
Chen, Jun; Bi, Shaohua; Wang, Juan; Dai, Liying
癫痫
神经科学
发表日期：2025
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The role of magnetic resonance imaging with diffusion tensor imaging in the evaluation of neurodevelopment in preterm infants

磁共振成像联合弥散张量成像在早产儿神经发育评估中的作用

期刊:Medicine
影响因子:1.4
doi:10.1097/MD.0000000000043482
Wang, Le; Bi, Shaohua; Zhang, Jian
发育与干细胞
神经科学
发表日期：2025
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Optical Genome Mapping Identifies a Novel Unbalanced Translocation Between Chromosomes 4q and 6q Leading to Feeding Difficulties and Hypotonia in a Neonate: A Case Report

光学基因组图谱鉴定出4q和6q染色体之间一种新的不平衡易位，导致新生儿喂养困难和肌张力低下：病例报告

期刊:Application of Clinical Genetics
影响因子:2.8
doi:10.2147/TACG.S465244
Wang, Ying; Bi, Shaohua; Shi, Xiaoqing; Dai, Liying
发表日期：2024
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Study on Sound-Insulation Performance of an Acoustic Metamaterial of Air-Permeable Multiple-Parallel-Connection Folding Chambers by Acoustic Finite Element Simulation

基于声学有限元模拟的透气多平行连接折叠腔声学超材料隔声性能研究

期刊:Materials
影响因子:3.2
doi:10.3390/ma16124298
Peng, Wenqiang; Bi, Shaohua; Shen, Xinmin; Yang, Xiaocui; Yang, Fei; Wang, Enshuai
发表日期：2023
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Effects of Aperture Shape on Absorption Property of Acoustic Metamaterial of Parallel-Connection Helmholtz Resonator

孔径形状对并联亥姆霍兹谐振器声学超材料吸收性能的影响

期刊:Materials
影响因子:3.2
doi:10.3390/ma16041597
Bi, Shaohua; Yang, Fei; Tang, Shuai; Shen, Xinmin; Zhang, Xiaonan; Zhu, Jingwei; Yang, Xiaocui; Peng, Wenqiang; Yuan, Feng
发表日期：2023
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Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations

中国东部24例早期婴儿癫痫性脑病的表型和遗传特征，包括1例罕见的UGDH双等位基因突变病例

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.2269
Jiang, Liangliang; Bi, Shaohua; Lin, Li; He, Fan; Deng, Fang
癫痫
神经科学
发表日期：2023
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Clinical report and genetic analysis of a Chinese neonate with craniofacial microsomia caused by a splicing variant of the splicing factor 3b subunit 2 gene.

中国新生儿颅面短小症的临床报告及基因分析，该病由剪接因子 3b 亚基 2 基因的剪接变异引起

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.2268
Zhang Yongli, Bi Shaohua, Dai Liying, Zhao Yuwei, Liu Yu, Shi Zifeng
其它
发表日期：2023
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Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

由Xp21.1邻近基因缺失综合征引起的杜氏肌营养不良症相关慢性肉芽肿病：病例报告及文献综述

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2022.970204
Bi, Shaohua; Dai, Liying; Jiang, Liangliang; Wang, Lili; Teng, Mia; Liu, Guanghui; Teng, Ru-Jeng
炎症/感染
发表日期：2022
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Transarterial Embolization in Neonatal Kasabach-Merritt Syndrome

新生儿卡萨巴赫-梅里特综合征的经动脉栓塞治疗

期刊:Frontiers in Pediatrics
影响因子:2
doi:10.3389/fped.2021.788120
Wang, Yinghao; Wang, Song; Wang, Lili; Bi, Shaohua; Zhang, Jian; Zha, Ping; Dai, Liying
发表日期：2021
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