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

Rare variants in NRSN2 cause non-syndromic orofacial cleft through dysregulation of TGF-β signaling

NRSN2基因的罕见变异通过TGF-β信号传导失调导致非综合征性唇腭裂。

期刊:Genes and Diseases
影响因子:
doi:10.1016/j.gendis.2025.101865
Zheng, Xiaowen; Liang, Xuqin; Wu, Xiantao; He, Qing; Yin, Chunyan; Jiao, Yuhua; Wang, Yanhao; Hou, Yuxia; Ding, Yi; Zhao, Huaxiang
TGF-β
信号转导
发表日期：2026
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Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.

外显子组测序揭示了非综合征性口面裂的遗传结构，并将BOC鉴定为一个新的致病基因

期刊:Advanced Science
影响因子:14.1
doi:10.1002/advs.202412073
He Qing, Yu Min, Jiao Yuhua, Xu Yizhu, Liang Xuqin, Huang Wenbin, Xu Linping, Hou Yuxia, Ren Zhanping, Lyu Beile, Qian Zhenwei, Liu Pengpeng, Zhou Jing, Huang Huimei, Yin Chunyan, Zhao Huaxiang, Ding Yi
其它
发表日期：2025
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Successful interdisciplinary retreatment after initial treatment failure in a cleft lip adolescent

唇裂青少年初次治疗失败后，跨学科再治疗取得成功

期刊:BMC Oral Health
影响因子:3.1
doi:10.1186/s12903-025-06055-6
Jiao, Yuhua; Tao, Yongwei; Du, Wenzhi; Zhu, Chunhui; Ren, Zhanping; Hou, Yuxia; Zhao, Huaxiang
发表日期：2025
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Editorial: The etiology and pathogenesis of craniomaxillofacial birth defects

社论：颅颌面出生缺陷的病因和发病机制

期刊:Frontiers in Dental Medicine
影响因子:1.8
doi:10.3389/fdmed.2025.1592762
Zhao, Huaxiang; Huang, Wenbin; Liu, Huan; Pan, Yongchu
发表日期：2025
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Whole-exome sequencing identifies ECPAS as a novel potentially pathogenic gene in multiple hereditary families with nonsyndromic orofacial cleft

全外显子组测序鉴定出 ECPAS 是多个患有非综合征性唇腭裂的遗传家族中一种新的潜在致病基因。

期刊:Protein & Cell
影响因子:12.8
doi:10.1093/procel/pwae021
Zhao, Huaxiang; Zhong, Wenjie; Huang, Wenbin; Ning, Guozhu; Zhang, Jieni; Zhang, Mengqi; Meng, Peiqi; Zhang, Yunfan; Zhang, Qian; Zhu, Hongping; Maimaitili, Gulibaha; Ding, Yi; Li, Weiran; Liang, Wei; Zhou, Zhibo; Wang, Qiang; Chen, Feng; Lin, Jiuxiang
发表日期：2024
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Efficacy of the maxillary anterior segmental distraction osteogenesis in patients with cleft lip and palate

上颌前段牵引成骨术治疗唇腭裂患者的疗效

期刊:BMC Oral Health
影响因子:3.1
doi:10.1186/s12903-024-05208-3
Pu, Panjun; Bao, Shanying; Gao, Jianbo; Jiao, Yuhua; Wang, Feiyu; Zhao, Huaxiang; Hou, Yuxia; Zhan, Yalin
发表日期：2024
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Treatment and genetic analysis of multiple supernumerary and impacted teeth in an adolescent patient

青少年患者多发性多生牙和阻生牙的治疗及基因分析

期刊:BMC Oral Health
影响因子:3.1
doi:10.1186/s12903-024-04573-3
Pu, Panjun; Hou, Yuxia; Zhang, Qing; Hu, Xiaoyi; Ding, Yi; Jia, Peizeng; Zhao, Huaxiang
发表日期：2024
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Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype-phenotype analysis

鉴定出导致中国某家族唇腭裂的罕见PTCH1无义变异，并进行了最新的基因型-表型分析

期刊:Genes and Diseases
影响因子:
doi:10.1016/j.gendis.2019.12.010
Zhong, Wenjie; Zhao, Huaxiang; Huang, Wenbin; Zhang, Mengqi; Zhang, Qian; Zhang, Yue; Chen, Chong; Nueraihemaiti, Zulihumaer; Tuerhong, Dilifeire; Huang, Huizhe; Maimaitili, Gulibaha; Chen, Feng; Lin, Jiuxiang
发表日期：2021
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A novel FZD6 mutation revealed the cause of cleft lip and/or palate in a Chinese family

一种新的FZD6基因突变揭示了中国一个家族唇腭裂的病因。

期刊:Genes and Diseases
影响因子:
doi:10.1016/j.gendis.2019.12.003
Zhang, Jieni; Zhao, Huaxiang; Huang, Wenbin; Song, Fengqi; Zhong, Wenjie; Zhang, Mengqi; Zhang, Yunfan; Zhou, Zhibo; Lin, Jiuxiang; Chen, Feng
发表日期：2020
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Is MTHFD1 polymorphism rs 2236225 (c.1958G>A) associated with the susceptibility of NSCL/P? A systematic review and meta-analysis

MTHFD1基因多态性rs2236225（c.1958G>A）与非综合征性唇腭裂的易感性相关吗？一项系统评价和荟萃分析

期刊:F1000Research
影响因子:
doi:10.12688/f1000research.6425.2
Zhao, Huaxiang; Zhang, Jieni; Zhang, Mengqi; Deng, Feng; Zheng, Leilei; Zheng, Hui; Chen, Feng; Lin, Jiuxiang
发表日期：2015
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