Knowledge structure and emerging trends in the application of deep learning in genetics research: A bibliometric analysis [2000–2021] von Zhang, Bijun, Fan, Ting

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Sponges of Carboxymethyl Chitosan Grafted with Collagen Peptides for Wound Healing von Cheng, Yu, Hu, Zhang, Zhao, Yuntao, Zou, Zuhao, Lu, Sitong, Zhang, Bijun, Li, Sidong

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An environmentally benign synthesis of isoxazolines and isoxazoles mediated by potassium chloride in water von Han, Liuquan, Zhang, Bijun, Zhu, Min, Yan, Jie

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Introduction on IMT-2020 5G Trials in China von Dong, Lei, Zhao, Hongyi, Chen, Yan, Chen, Dageng, Wang, Tianxiang, Lu, Lei, Zhang, Bijun, Hu, Liang, Gu, Liang, Li, Bojie, Yang, Huilian, Shen, Hui, Tian, Tingjian, Luo, Zhendong, Wei, Kejun

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Design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructures von Zhang, Bijun, Vogt, Martin, Maggiora, Gerald M., Bajorath, Jürgen

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Renal NKCC2 Is Dual Regulated by the Synergy of 20-HETE and High-Fat Diet in CYP4F2 Transgenic Mice von Wu, Jingjing, Lai, Guangrui, Chen, Fangjie, Zhang, Bijun, Zhao, Yanyan

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Nedd4-2 Haploinsufficiency in Mice Impairs the Ubiquitination of Rer1 and Increases the Susceptibility to Endoplasmic Reticulum Stress and Seizures von Liu, Xiaoliang, Zhang, Lu, Zhang, Hebo, Liang, Xiaoyan, Zhang, Bijun, Tu, Jianqiao, Zhao, Yanyan

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Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report von Liu, Xiaoliang, Sun, Wei, Wang, Jun, Chu, Guoming, He, Rong, Zhang, Bijun, Zhao, Yanyan

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Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome von Zhang, Lu, Liu, Xiaoliang, Zhao, Yunjing, Wang, Qingyi, Zhang, Yuanyuan, Gao, Haiming, Zhang, Bijun, Cui, Wanting, Zhao, Yanyan

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Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders von Zhang, Yuanyuan, Liu, Xiaoliang, Gao, Haiming, Cui, Wanting, Zhang, Bijun, Zhao, Yanyan

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AnalogExplorer: A New Method for Graphical Analysis of Analog Series and Associated Structure–Activity Relationship Information von Zhang, Bijun, Hu, Ye, Bajorath, Jürgen

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Nonsense suppression induced readthrough of a novel PAX6 mutation in patient‐derived cells of congenital aniridia von Liu, Xiaoliang, Zhang, Yuanyuan, Zhang, Bijun, Gao, Haiming, Qiu, Chuang

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Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1 von Wang, Jianda, Hou, Yanqi, Qi, Lina, Zhai, Shuang, Zheng, Liangwu, Han, Lin, Guo, Yufan, Zhang, Bijun, Miao, Pu, Lou, Yuting, Xu, Xiaoxiao, Wang, Ye, Ren, Yanqi, Cao, Zhenhua, Feng, Jianhua

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Systematic Assessment of Compound Series with SAR Transfer Potential von Zhang, Bijun, Wassermann, Anne Mai, Vogt, Martin, Bajorath, Jürgen

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Novel variant of ETFDH leading to multiple acyl-CoA dehydrogenase deficiency by promoting protein degradation via ubiquitin proteasome pathway von Zhang, Bijun, Zhao, Yanyan

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Hypervalent Iodine Catalyzed Cyclization of Aryl-Substituted Alkanoic Acids von Li, Tingting, Xiang, Changbin, Zhang, Bijun, Yan, Jie

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Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation von Guo, Yufan, Wang, Jianda, Wang, ZhiLiang, Lou, Yuting, Chen, Wangyang, Sheng, Min, Wang, Ye, Zhang, Bijun, Gao, Liuyan, Feng, Jianhua

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SAR Transfer across Different Targets von Zhang, Bijun, Hu, Ye, Bajorath, Jürgen

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Hierarchical mining algorithm for high dimensional spatiotemporal big data based on association rules von Zhou, Chunlei, Dong, Xinwei, Ji, Liang, Zhang, Bijun, Xu, Zhongping, Zhang, Chengping

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Electrophysiological features: The next precise step for SCN2A developmental epileptic encephalopathy von Miao, Pu, Tang, Siyang, Ye, Jia, Wang, Jianda, Lou, Yuting, Zhang, Bijun, Xu, Xiaoxiao, Chen, Xiaoquan, Li, Yuezhou, Feng, Jianhua

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