A rare Coffin-Siris syndrome induced by SOX11: a de novo nonsense variant of short stature von Bai, Guibin, Yuan, Rougang, Yuan, Jian, Liu, Yanqin, Zhao, Shaozhi, Zhang, Xinwen

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Compound heterozygous variants of the SLC26A4 gene in a Chinese family with enlarged vestibular aqueducts von He, Xiaohui, Zhao, Shaozhi, Shi, Lin, Lu, Yitong, Yang, Yintong, Zhang, Xinwen

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A Nonsense Variant of ZNF462 Gene Associated With Weiss-Kruszka Syndrome-Like Manifestations: A Case Study and Literature Review von Zhao, Shaozhi, Miao, Chen, Wang, Xiaolei, Lu, Yitong, Liu, Hongwei, Zhang, Xinwen

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Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiency von Lu, Yitong, Zhao, Shaozhi, He, Xiaohui, Yang, Hua, Wang, Xiaolei, Miao, Chen, Liu, Hongwei, Zhang, Xinwen

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Radiomics Analysis for Predicting Epilepsy in Patients With Unruptured Brain Arteriovenous Malformations von Zhao, Shaozhi, Zhao, Qi, Jiao, Yuming, Li, Hao, Weng, Jiancong, Huo, Ran, Wang, Jie, Xu, Hongyuan, Zhang, Junze, Li, Yan, Wu, Zhenzhou, Wang, Shuo, Cao, Yong, Zhao, Jizong

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Cerebral vascular malformations: pathogenesis and therapy von He, Qiheng, Huo, Ran, Sun, Yingfan, Zheng, Zhiyao, Xu, Hongyuan, Zhao, Shaozhi, Ni, Yang, Yu, Qifeng, Jiao, Yuming, Zhang, Wenqian, Zhao, Jizong, Cao, Yong

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KRAS mutation-induced EndMT of brain arteriovenous malformation is mediated through the TGF-β/BMP-SMAD4 pathway von Xu, Hongyuan, Huo, Ran, Li, Hao, Jiao, Yuming, Weng, Jiancong, Wang, Jie, Yan, Zihan, Zhang, Junze, Zhao, Shaozhi, He, Qiheng, Sun, Yingfan, Wang, Shuo, Cao, Yong

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Genotype‐phenotype correlations in multiple lesions of familial cerebral cavernous malformations concerning phosphatidylinositol 3‐kinase catalytic subunit alpha mutations von Wang, Jie, Tang, Jihong, Yang, Yingxi, Jiao, Yuming, Huo, Ran, Xu, Hongyuan, Zhao, Shaozhi, Sun, Yingfan, He, Qiheng, Yu, Qifeng, Wang, Shuo, Zhao, Jizong, Wang, Jiguang, Cao, Yong

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Somatic GJA4 mutation in intracranial extra-axial cavernous hemangiomas von Huo, Ran, Yang, Yingxi, Xu, Hongyuan, Zhao, Shaozhi, Song, Dong, Weng, Jiancong, Ma, Ruochen, Sun, Yingfan, Wang, Jie, Jiao, Yuming, Zhang, Junze, He, Qiheng, Wu, Ruolei, Wang, Shuo, Zhao, Ji-Zong, Zhang, Junting, Wang, Jiguang, Cao, Yong

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Therapy management and outcome of acute hydrocephalus secondary to intraventricular hemorrhage in adults von Wang, Chaoyang, Bai, Jianuo, He, Qiheng, Jiao, Yuming, Zhang, Wenqian, Huo, Ran, Wang, Jie, Xu, Hongyuan, Zhao, Shaozhi, Wu, Zhiyou, Sun, Yingfan, Yu, Qifeng, Tang, Jinyi, Zeng, Xianwei, Yang, Wuyang, Cao, Yong

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Grading scale based on arcuate fasciculus segmentation to predict postoperative language outcomes of brain arteriovenous malformations von Jiao, Yuming, Zhao, Shaozhi, Li, Hao, Wu, Jun, Weng, Jiancong, Huo, Ran, Wang, Jie, Wang, Shuo, Cao, Yong, Zhao, Ji Zong

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Identification and analysis of biomarkers associated with oxidative stress and ferroptosis in recurrent miscarriage von Xie, Jinxia, Zhu, Hongli, Zhao, Shaozhi, Ma, Yongqin, Shi, Panpan, Zhan, Xuxin, Tian, Wenyan, Wang, Yingmei

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The role of ApoE in fatty acid transport from neurons to astrocytes under ischemia/hypoxia conditions von Chen, Hongyan, Zhao, Shaozhi, Jian, Qiang, Yan, Yinfang, Wang, Simin, Zhang, Xinwen, Ji, Yuqiang

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Exosomal miR‐3131 derived from endothelial cells with KRAS mutation promotes EndMT by targeting PICK1 in brain arteriovenous malformations von He, Qiheng, Huo, Ran, Wang, Jie, Xu, Hongyuan, Zhao, Shaozhi, Zhang, Junze, Sun, Yingfan, Jiao, Yuming, Weng, Jiancong, Zhao, Jizong, Cao, Yong

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Endothelial hyperactivation of mutant MAP3K3 induces cerebral cavernous malformation enhanced by PIK3CA GOF mutation von Huo, Ran, Yang, Yingxi, Sun, Yingfan, Zhou, Qiuxia, Zhao, Shaozhi, Mo, Zongchao, Xu, Hongyuan, Wang, Jie, Weng, Jiancong, Jiao, Yuming, Zhang, Junze, He, Qiheng, Wang, Shuo, Zhao, Jizong, Wang, Jiguang, Cao, Yong

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Identification of a novel homozygous loss-of-function mutation in FUCA1 gene causing severe fucosidosis: A case report von Zhang, Xinwen, Zhao, Shaozhi, Liu, Hongwei, Wang, Xiaoyan, Wang, Xiaolei, Du, Nan, Liu, Hui, Duan, Hongfang

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Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot-Marie-Tooth Disease Type 4B1 von Du, Nan, Wang, Xiaolei, Wang, Zhaohui, Liu, Hongwei, Liu, Hui, Duan, Hongfang, Zhao, Shaozhi, Banerjee, Santasree, Zhang, Xinwen

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Identification of a novel homozygous mutation in gene causing severe fucosidosis: A case report von Xinwen Zhang, Shaozhi Zhao, Hongwei Liu, Xiaoyan Wang, Xiaolei Wang, Nan Du, Hui Liu, Hongfang Duan

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Identifying mRNAs Bound by Human RBMY Protein in the Testis von ZENG, Mei, LIANG, Suhua, ZHAO, Shaozhi, LIU, Yanyan, SUN, Huaqin, ZHANG, Sizhong, MA, Yongxin

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Method and device of determining distance and height based on a plurality of sensors von Wu, Xianghao, Zhang, Haitao, Chen, Zhiqiang, Dai, Jundi, Zhao, Shaozhi, Li, Yuanjing, An, Guocheng

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