Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome
Luo, Minna, Lin, Zaisheng, Zhu, Tian, Jin, Minjun, Meng, Dan, He, Ruida, Cao, Zongfu, Shen, Yue, Lu, Chao, Cai, Ruikun, Zhao, Yong, Wang, Xueyan, Li, Hui, Wu, Shijing, Zou, Xuan, Luo, Guanjun, Cao, Li, Huang, Min, Jiao, Huike, Gao, Huafang, Sui, Ruifang, Zhao, Chengtian, Ma, Xu, Cao, Muqing
Published in Genetics in medicine (01.06.2021)
Published in Genetics in medicine (01.06.2021)
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Molecular diagnose of a large hearing loss population from China by targeted genome sequencing
Wu, Jie, Cao, Zongfu, Su, Yu, Wang, Yang, Cai, Ruikun, Chen, Jiyue, Gao, Bo, Han, Mingyu, Li, Xiaohong, Zhang, DeJun, Gao, Xue, Huang, Shasha, Huang, Quanfei, Yuan, Yongyi, Ma, Xu, Dai, Pu
Published in Journal of human genetics (01.11.2022)
Published in Journal of human genetics (01.11.2022)
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Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome
Shen, Yue, Wang, Hao, Liu, Zhimin, Luo, Minna, Ma, Siyu, Lu, Chao, Cao, Zongfu, Yu, Yufei, Cai, Ruikun, Chen, Cuixia, Li, Qian, Gao, Huafang, Peng, Yun, Xu, Baoping, Ma, Xu
Published in BMC medical genetics (01.10.2020)
Published in BMC medical genetics (01.10.2020)
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Correction to: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome
Luo, Minna, Lin, Zaisheng, Zhu, Tian, Jin, Minjun, Meng, Dan, He, Ruida, Cao, Zongfu, Shen, Yue, Lu, Chao, Cai, Ruikun, Zhao, Yong, Wang, Xueyan, Li, Hui, Wu, Shijing, Zou, Xuan, Luo, Guanjun, Cao, Li, Huang, Min, Jiao, Huike, Gao, Huafang, Sui, Ruifang, Zhao, Chengtian, Ma, Xu, Cao, Muqing
Published in Genetics in medicine (01.06.2021)
Published in Genetics in medicine (01.06.2021)
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Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy
Chuan, Zhang, Ruikun, Cai, Qian, Li, Shiyue, Mei, Shengju, Hao, Yong, Yuan, Haibo, Li, Neng, Xiao, Yong, Zhao, Huiqin, Xue, Weijia, Wang, Ling, Hui, Bingbo, Zhou, Zhang, Qinghua, Yan, Wang, Zongfu, Cao, Xu, Ma
Published in Frontiers in genetics (27.04.2022)
Published in Frontiers in genetics (27.04.2022)
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Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome
Cai, Ruikun, Dong, Yichao, Fang, Mingxia, Fan, Yuxuan, Cheng, Zian, Zhou, Yue, Gao, Jianen, Han, Feifei, Guo, Changlong, Ma, Xu
Published in Frontiers in cell and developmental biology (18.03.2021)
Published in Frontiers in cell and developmental biology (18.03.2021)
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Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants
Zhang, Xiujuan, Shen, Yue, Li, Ping, Cai, Ruikun, Lu, Chao, Li, Qian, Chen, Cuixia, Yu, Yufei, Cheng, Tingting, Wang, Xian, Luo, Minna, Cao, Muqing, Cao, Zongfu, Ma, Xu
Published in Molecular genetics & genomic medicine (01.06.2021)
Published in Molecular genetics & genomic medicine (01.06.2021)
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High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood
Guo, Changlong, MD, PhD, Wang, Qidi, MD, PhD, Cao, Xiaofang, MD, Yang, Ying, MD, PhD, Liu, Xin, PhD, An, Lisha, MD, Cai, Ruikun, PhD, Du, Meng, MD, Wang, Guangyu, MD, Qiu, Yue, MD, Peng, Zuoqi, MD, Han, Jian, MD, PhD, Ni, Shuhua, PhD, Tan, Xuerui, MD, PhD, Jin, Li, MD, Yu, Song, MD, Wang, Huiying, MD, Wang, Chunlin, PhD, Wang, Xingyu, MD, PhD, Ma, Xu, MD, PhD
Published in The Journal of pediatrics (01.09.2016)
Published in The Journal of pediatrics (01.09.2016)
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GPS-MBA: computational analysis of MHC class II epitopes in type 1 diabetes
Cai, Ruikun, Liu, Zexian, Ren, Jian, Ma, Chuang, Gao, Tianshun, Zhou, Yanhong, Yang, Qing, Xue, Yu
Published in PloS one (27.03.2012)
Published in PloS one (27.03.2012)
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Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome
Luo, Minna, Cao, Li, Cao, Zongfu, Ma, Siyu, Shen, Yue, Yang, Di, Lu, Chao, Lin, Zaisheng, Liu, Zhimin, Yu, Yufei, Cai, Ruikun, Chen, Cuixia, Gao, Huafang, Wang, Xueyan, Cao, Muqing, Ma, Xu
Published in Molecular genetics & genomic medicine (01.12.2019)
Published in Molecular genetics & genomic medicine (01.12.2019)
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A defined serum-free culture system for human long-term haematopoietic stem cells
Dong, Yichao, Cai, Ruikun, Fang, Mingxia, Chen, Yuqi, Li, Peng, Guo, Changlong, Ma, Xu
Published in British journal of haematology (01.01.2024)
Published in British journal of haematology (01.01.2024)
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Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia
Guo, Changlong, Cai, Ruikun, Cao, Xiaofang, Yang, Ying, Wang, Qidi, He, Runsheng, An, Lisha, Peng, Zuoqi, Chen, Yequn, Ni, Shuhua, Tan, Xuerui, Han, Jian, Liu, Xin, Lin, Li, Yu, Song, Wang, Xingyu, Wang, Chunlin, Ma, Xu
Published in Human immunology (01.10.2019)
Published in Human immunology (01.10.2019)
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High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris
Cao, Xiaofang, Wa, Qingbiao, Wang, Qidi, Li, Lin, Liu, Xin, An, Lisha, Cai, Ruikun, Du, Meng, Qiu, Yue, Han, Jian, Wang, Chunlin, Wang, Xingyu, Guo, Changlong, Lu, Yonghong, Ma, Xu
Published in International immunopharmacology (01.11.2016)
Published in International immunopharmacology (01.11.2016)
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Journal Article
Correction: GPS-MBA: Computational Analysis of MHC Class II Epitopes in Type 1 Diabetes
Cai, Ruikun, Liu, Zexian, Ren, Jian, Ma, Chuang, Gao, Tianshun, Zhou, Yanhong, Yang, Qing, Xue, Yu
Published in PloS one (09.08.2012)
Published in PloS one (09.08.2012)
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VarfromPDB: An Automated and Integrated Tool to Mine Disease-Gene-Variant Relations from the Public Databases and Literature
Cao, Zongfu, Wang, Lei, Chen, Yilu, Cai, Ruikun, Lu, Jianbo, Yu, Yufei, Chen, Cuixia, Gu, Feng, Yang, Juhua, Ma, Xu
Published in Journal of proteomics & bioinformatics (2017)
Published in Journal of proteomics & bioinformatics (2017)
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Journal Article
Sequence similarity analysis of non-self CTL epitopes and mouse proteins using sequence alignment
Cai, Ruikun, Cheng, Xi, Ma, Chuang, Zhou, Yanhong
Published in Wuhan University journal of natural sciences (01.02.2011)
Published in Wuhan University journal of natural sciences (01.02.2011)
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