Data Mining Suggests That CXCL14 Gene Silencing in Colon Cancer Is Due to Promoter Methylation
Wang, Yanjing, Wang, Siyi, Niu, Yuchen, Ma, Buyong, Li, Jingjing
Published in International journal of molecular sciences (01.11.2023)
Published in International journal of molecular sciences (01.11.2023)
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A Hybrid Rule-Based and Data-Driven Approach to Illegal Transshipment Identification with Interpretable Behavior Features
Deng, Lei, Niu, Yuchen, Jia, Limin, Liu, Wen, Zang, Yu
Published in Sensors (Basel, Switzerland) (07.12.2022)
Published in Sensors (Basel, Switzerland) (07.12.2022)
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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
Liu, Jiaqi, Wu, Nan, Yang, Nan, Takeda, Kazuki, Chen, Weisheng, Li, Weiyu, Du, Renqian, Liu, Sen, Zhou, Yangzhong, Zhang, Ling, Liu, Zhenlei, Zuo, Yuzhi, Zhao, Sen, Blank, Robert, Pehlivan, Davut, Dong, Shuangshuang, Zhang, Jianguo, Shen, Jianxiong, Si, Nuo, Wang, Yipeng, Liu, Gang, Li, Shugang, Zhao, Yanxue, Zhao, Hong, Chen, Yixin, Zhao, Yu, Song, Xiaofei, Hu, Jianhua, Lin, Mao, Tian, Ye, Yuan, Bo, Yu, Keyi, Niu, Yuchen, Yu, Bin, Li, Xiaoxin, Chen, Jia, Yan, Zihui, Zhu, Qiankun, Meng, Xiaolu, Chen, Xiaoli, Su, Jianzhong, Zhao, Xiuli, Wang, Xiaoyue, Ming, Yue, Li, Xiao, Raggio, Cathleen L., Zhang, Baozhong, Weng, Xisheng, Zhang, Shuyang, Zhang, Xue, Watanabe, Kota, Matsumoto, Morio, Jin, Li, Shen, Yiping, Sobreira, Nara L., Posey, Jennifer E., Giampietro, Philip F., Valle, David, Liu, Pengfei, Wu, Zhihong, Ikegawa, Shiro, Lupski, James R., Zhang, Feng, Qiu, Guixing
Published in Genetics in medicine (01.07.2019)
Published in Genetics in medicine (01.07.2019)
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Identification of novel FBN1 variations implicated in congenital scoliosis
Lin, Mao, Zhao, Sen, Liu, Gang, Huang, Yingzhao, Yu, Chenxi, Zhao, Yanxue, Wang, Lianlei, Zhang, Yuanqiang, Yan, Zihui, Wang, Shengru, Liu, Sen, Liu, Jiaqi, Ye, Yongyu, Chen, Yaping, Yang, Xu, Tong, Bingdu, Wang, Zheng, Yang, Xinzhuang, Niu, Yuchen, Li, Xiaoxin, Wang, Yipeng, Su, Jianzhong, Yuan, Jian, Zhao, Hengqiang, Zhang, Shuyang, Qiu, Guixing, Ikegawa, Shiro, Zhang, Jianguo, Wu, Zhihong, Wu, Nan
Published in Journal of human genetics (01.03.2020)
Published in Journal of human genetics (01.03.2020)
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A genotype-first analysis in a cohort of Mullerian anomaly
Tian, Weijie, Chen, Na, Ye, Yang, Ma, Congcong, Qin, Chenglu, Niu, Yuchen, Xiaoxin, L, Zhao, Lina, Zhao, Hengqiang, Liang, Ze, Song, Shuang, Wang, Yuan, Chen, Zefu, Lin, Jiachen, Yan, Zihui, Duan, Jiali, Zhao, Sen, Zhang, Terry Jianguo, Qiu, Guixing, Wu, Zhihong, Wu, Nan, Zhu, Lan
Published in Journal of human genetics (01.06.2022)
Published in Journal of human genetics (01.06.2022)
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Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine
Zhao, Sen, Zhao, Hengqiang, Zhao, Lina, Cheng, Xi, Zheng, Zhifa, Wu, Mengfan, Wen, Wen, Wang, Shengru, Zhou, Zixiang, Xie, Haibo, Ruan, Dengfeng, Li, Qing, Liu, Xinquan, Ou, Chengzhu, Li, Guozhuang, Zhao, Zhengye, Chen, Guilin, Niu, Yuchen, Yin, Xiangjie, Hu, Yuhong, Zhang, Xiaochen, Liu, Pengfei, Qiu, Guixing, Liu, Wanlu, Zhao, Chengtian, Wu, Zhihong, Zhang, Jianguo, Wu, Nan
Published in Nature communications (06.02.2024)
Published in Nature communications (06.02.2024)
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Journal Article
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
Li, Ziquan, Zhao, Sen, Cai, Siyi, Zhang, Yuanqiang, Wang, Lianlei, Niu, Yuchen, Li, Xiaoxin, Hu, Jianhua, Chen, Jingdan, Wang, Shengru, Wang, Huizi, Liu, Gang, Tian, Ye, Wu, Zhihong, Zhang, Terry Jianguo, Wang, Yipeng, Wu, Nan
Published in BMC musculoskeletal disorders (11.04.2020)
Published in BMC musculoskeletal disorders (11.04.2020)
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Disruptive NADSYN1 Variants Implicated in Congenital Vertebral Malformations
Lin, Jiachen, Zhao, Lina, Zhao, Sen, Li, Shengjie, Zhao, Zhengye, Chen, Zefu, Zheng, Zhifa, Shao, Jiashen, Niu, Yuchen, Li, Xiaoxin, Zhang, Jianguo Terry, Wu, Zhihong, Wu, Nan
Published in Genes (14.10.2021)
Published in Genes (14.10.2021)
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Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis
Liu, Gang, Wang, Lianlei, Wang, Xinyu, Yan, Zihui, Yang, Xinzhuang, Lin, Mao, Liu, Sen, Zuo, Yuzhi, Niu, Yuchen, Zhao, Sen, Zhao, Yanxue, Zhang, Jianguo, Shen, Jianxiong, Wang, Yipeng, Qiu, Guixing, Wu, Zhihong, Wu, Nan
Published in Frontiers in bioengineering and biotechnology (10.12.2019)
Published in Frontiers in bioengineering and biotechnology (10.12.2019)
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Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis
Liu, Gang, Zhao, Hengqiang, Yan, Zihui, Zhao, Sen, Niu, Yuchen, Li, Xiaoxin, Wang, Shengru, Yang, Yang, Liu, Sen, Zhang, Terry Jianguo, Wu, Zhihong, Wu, Nan
Published in Molecular therapy. Nucleic acids (05.03.2021)
Published in Molecular therapy. Nucleic acids (05.03.2021)
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Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Wang, Kun, Zhao, Sen, Zhang, Qianqian, Yuan, Jian, Liu, Jiaqi, Ding, Xinghuan, Song, Xiaofei, Lin, Jiachen, Du, Renqian, Zhou, Yangzhong, Sugimoto, Michihiko, Chen, Weisheng, Yuan, Bo, Liu, Jian, Yan, Zihui, Liu, Bowen, Zhang, Yisen, Li, Xiaoxin, Niu, Yuchen, Long, Bo, Shen, Yiping, Zhang, Shuyang, Abe, Kuniya, Su, Jianzhong, Wu, Zhihong, Wu, Nan, Liu, Pengfei, Yang, Xinjian
Published in Journal of human genetics (01.11.2018)
Published in Journal of human genetics (01.11.2018)
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Journal Article
Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly
Sun, Liying, Huang, Yingzhao, Zhao, Sen, Zhong, Wenyao, Shi, Jile, Guo, Yang, Zhao, Junhui, Xiong, Ge, Yin, Yuehan, Chen, Zefu, Zhang, Nan, Zhao, Zongxuan, Li, Qingyang, Chen, Dan, Niu, Yuchen, Li, Xiaoxin, Qiu, Guixing, Wu, Zhihong, Zhang, Terry Jianguo, Tian, Wen, Wu, Nan
Published in Frontiers in genetics (10.03.2022)
Published in Frontiers in genetics (10.03.2022)
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Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders
Zhao, Sen, Zhang, Yuanqiang, Hallgrimsdottir, Sigrun, Zuo, Yuzhi, Li, Xiaoxin, Batkovskyte, Dominyka, Liu, Sen, Lindelöf, Hillevi, Wang, Shengru, Hammarsjö, Anna, Yang, Yang, Ye, Yongyu, Wang, Lianlei, Yan, Zihui, Lin, Jiachen, Yu, Chenxi, Chen, Zefu, Niu, Yuchen, Wang, Huizi, Zhao, Zhi, Liu, Pengfei, Qiu, Guixing, Posey, Jennifer E, Wu, Zhihong, Lupski, James R, Micule, Ieva, Anderlid, Britt-Marie, Voss, Ulrika, Sulander, Dennis, Kuchinskaya, Ekaterina, Nordgren, Ann, Nilsson, Ola, Zhang, Terry Jianguo, Grigelioniene, Giedre, Wu, Nan
Published in Npj genomic medicine (15.02.2022)
Published in Npj genomic medicine (15.02.2022)
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The Mutational Landscape of PTK7 in Congenital Scoliosis and Adolescent Idiopathic Scoliosis
Su, Zhe, Yang, Yang, Wang, Shengru, Zhao, Sen, Zhao, Hengqiang, Li, Xiaoxin, Niu, Yuchen, Deciphering Disorders Involving Scoliosis And COmorbidities Disco Study Group, Qiu, Guixing, Wu, Zhihong, Wu, Nan, Zhang, Terry Jianguo
Published in Genes (12.11.2021)
Published in Genes (12.11.2021)
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Journal Article
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia
Shao, Jiashen, Zhao, Sen, Yan, Zihui, Wang, Lianlei, Zhang, Yuanqiang, Lin, Mao, Yu, Chenxi, Wang, Shengru, Niu, Yuchen, Li, Xiaoxin, Qiu, Guixing, Zhang, Jianguo, Wu, Zhihong, Wu, Nan
Published in BMC medical genetics (27.05.2020)
Published in BMC medical genetics (27.05.2020)
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Journal Article
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Chen, Zefu, Yan, Zihui, Yu, Chenxi, Liu, Jiaqi, Zhang, Yanbin, Zhao, Sen, Lin, Jiachen, Zhang, Yuanqiang, Wang, Lianlei, Lin, Mao, Huang, Yingzhao, Li, Xiaoxin, Niu, Yuchen, Wang, Shengru, Wu, Zhihong, Qiu, Guixing, Zhang, Terry Jianguo, Wu, Nan
Published in Orphanet journal of rare diseases (15.09.2020)
Published in Orphanet journal of rare diseases (15.09.2020)
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Journal Article
Novel FGFR1 Variants Are Associated with Congenital Scoliosis
Wang, Shengru, Chai, Xiran, Yan, Zihui, Zhao, Sen, Yang, Yang, Li, Xiaoxin, Niu, Yuchen, Lin, Guanfeng, Su, Zhe, Wu, Zhihong, Zhang, Terry Jianguo, Wu, Nan
Published in Genes (24.07.2021)
Published in Genes (24.07.2021)
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Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Yu, Chenxi, Xie, Bobo, Zhao, Zhengye, Zhao, Sen, Liu, Lian, Cheng, Xi, Li, Xiaoxin, Cao, Bingyan, Shao, Jiashen, Chen, Jiajia, Zhao, Hengqiang, Yan, Zihui, Su, Chang, Niu, Yuchen, Song, Yanning, Wei, Liya, Wang, Yi, Ren, Xiaoya, Fan, Lijun, Zhang, Beibei, Li, Chuan, Gui, Baoheng, Zhang, Yuanqiang, Wang, Lianlei, Chen, Shaoke, Zhang, Jianguo, Wu, Zhihong, Gong, Chunxiu, Fan, Xin, Wu, Nan
Published in Frontiers in endocrinology (Lausanne) (13.09.2021)
Published in Frontiers in endocrinology (Lausanne) (13.09.2021)
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Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism
Liu, Bowen, Zhao, Sen, Yan, Zihui, Zhao, Lina, Lin, Jiachen, Wang, Shengru, Niu, Yuchen, Li, Xiaoxin, Qiu, Guixing, Zhang, Terry Jianguo, Wu, Zhihong, Wu, Nan
Published in Frontiers in cell and developmental biology (19.03.2021)
Published in Frontiers in cell and developmental biology (19.03.2021)
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