Xiao-Jin He (Xiaojin He)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 30

Top Venues

Journal of medical genetics

Nature communications

Clinical genetics

Cell death & disease

This page only lists publications with an associated author ORCID identifier.

Publications

Yong-Wei Xiong, Hua-Long Zhu, Jin Zhang, Hao Geng, Lu-Lu Tan, Xin-Mei Zheng, Hao Li, Long-Long Fan, Xin-Run Wang, Xu-Dong Zhang, Kai-Wen Wang, Wei Chang, Yu-Feng Zhang, Zhi Yuan, Zong-Liu Duan, Yun-Xia Cao, Xiao-Jin He, De-Xiang Xu, Hua Wang
Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification. Nature communications 15 (1) (2024)
Yang Gao, Rufeng Xue, Rui Guo, Fan Yang, Xuan Sha, Yuqian Li, Rong Hua, Guotong Li, Qunshan Shen, Kuokuo Li, Wenwen Liu, Yuping Xu, Ping Zhou, ZhaoLian Wei, Zhiguo Zhang, Yun-Xia Cao, Xiao-Jin He, Huan Wu
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches. Human reproduction (Oxford, England) (2024)
Dan Liang, Rui Yan, Xin Long, Dongmei Ji, Bing Song, Mengyao Wang, Fan Zhang, Xin Cheng, Fengyuan Sun, Ran Zhu, Xinling Hou, Tianjuan Wang, Weiwei Zou, Ying Zhang, Zhixin Pu, Jing Zhang, Zhiguo Zhang, Yajing Liu, Yuqiong Hu, Xiao-Jin He, Yun-Xia Cao, Fan Guo
Distinct dynamics of parental 5-hydroxymethylcytosine during human preimplantation development regulate early lineage gene expression. Nature cell biology (2024)
Yong-Wei Xiong, Hua-Long Zhu, Jin Zhang, Hao Geng, Lu-Lu Tan, Xin-Mei Zheng, Hao Li, Long-Long Fan, Xin-Run Wang, Xu-Dong Zhang, Kai-Wen Wang, Wei Chang, Yu-Feng Zhang, Zhi Yuan, Zong-Liu Duan, Yun-Xia Cao, Xiao-Jin He, De-Xiang Xu, Hua Wang
Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification. Nature communications 15 (1) (2024)
Yang Gao, Liting Liu, Shixiong Tian, Chunyu Liu, Mingrong Lv, Huan Wu, Dongdong Tang, Bing Song, Qunshan Shen, Yuping Xu, Ping Zhou, Zhaolian Wei, Feng Zhang, Yunxia Cao, Xiao-Jin He
Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization. Andrology (2024)
Yong-Wei Xiong, Hua-Long Zhu, Jin Zhang, Hao Geng, Lu-Lu Tan, Xin-Mei Zheng, Hao Li, Long-Long Fan, Xin-Run Wang, Xu-Dong Zhang, Kai-Wen Wang, Wei Chang, Yu-Feng Zhang, Zhi Yuan, Zong-Liu Duan, Yun-Xia Cao, Xiao-Jin He, De-Xiang Xu, Hua Wang
Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification. Nature communications 15 (1) (2024)
Yong-Wei Xiong, Hua-Long Zhu, Jin Zhang, Hao Geng, Lu-Lu Tan, Xin-Mei Zheng, Hao Li, Long-Long Fan, Xin-Run Wang, Xu-Dong Zhang, Kai-Wen Wang, Wei Chang, Yu-Feng Zhang, Zhi Yuan, Zong-Liu Duan, Yun-Xia Cao, Xiao-Jin He, De-Xiang Xu, Hua Wang
Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification. Nature communications 15 (1) (2024)
Yong-Wei Xiong, Hua-Long Zhu, Jin Zhang, Hao Geng, Lu-Lu Tan, Xin-Mei Zheng, Hao Li, Long-Long Fan, Xin-Run Wang, Xu-Dong Zhang, Kai-Wen Wang, Wei Chang, Yu-Feng Zhang, Zhi Yuan, Zong-Liu Duan, Yun-Xia Cao, Xiao-Jin He, De-Xiang Xu, Hua Wang
Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification. Nature communications 15 (1) (2024)
Yuqian Li, Qiang Zhang, Qing Tan, Xuan Sha, Yang Gao, Rong Hua, Ping Zhou, Zhaolian Wei, Xiao-Jin He, Yunxia Cao, Tao Li, Huan Wu
LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes. Clinical genetics (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Shixiong Tian, Chaofeng Tu, Xiao-Jin He, Lanlan Meng, Jiaxiong Wang, Shuyan Tang, Yang Gao, Chunyu Liu, Huan Wu, Yiling Zhou, Mingrong Lv, Jing Guo, Li Jin, Yunxia Cao, Dongdong Tang, Feng Zhang, Yue-Qiu Tan
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. Journal of medical genetics (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Fei Tang, Yang Gao, KuoKuo Li, DongDong Tang, Yan Hao, Mingrong Lv, Huan Wu, Huiru Cheng, Jia Fei, Zhiping Jin, Chao Wang, Yuping Xu, Zhaolian Wei, Ping Zhou, Tingting Ye, Xiao-Jin He, Yun-Xia Cao
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos. Journal of assisted reproduction and genetics (2023)
Rong Hua, Rufeng Xue, Yiyuan Liu, Yuqian Li, Xuan Sha, Kuokuo Li, Yang Gao, Qunshan Shen, Mingrong Lv, Yuping Xu, Zhiguo Zhang, Xiao-Jin He, Yun-Xia Cao, Huan Wu
ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida. Human reproduction (Oxford, England) (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Huan Wu, Yiyuan Liu, Yuqian Li, Kuokuo Li, Chuan Xu, Yang Gao, Mingrong Lv, Rui Guo, Yuping Xu, Ping Zhou, Zhaolian Wei, Rong Hua, Xiao-Jin He, Yun-Xia Cao
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath. Cell death & disease 14 (2) (2023)
Xiaoyu Zhu, Kaiqin Hu, Huiru Cheng, Huan Wu, Kuokuo Li, Yang Gao, Mingrong Lv, Chuan Xu, Hao Geng, Qunshan Shen, Yunxia Cao, Xiao-Jin He, Dongdong Tang, Rui Guo
Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia. Clinical genetics (2023)
Dongdong Tang, Kuokuo Li, Hao Geng, Chuan Xu, Mingrong Lv, Yang Gao, Guanxiong Wang, Hui Yu, Zhongmei Shao, Qunshan Shen, Hui Jiang, Xiansheng Zhang, Xiao-Jin He, Yunxia Cao
Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia. Reproductive biology and endocrinology : RB&E 20 (1) (2022)
Guanxiong Wang, Xiaoyu Zhu, Yang Gao, Mingrong Lv, Kuokuo Li, Dongdong Tang, Huan Wu, Chuan Xu, Hao Geng, Qunshan Shen, Xiaomin Zha, Zongliu Duan, Jingjing Zhang, Rong Hua, Fangbiao Tao, Ping Zhou, Zhaolian Wei, Yunxia Cao, Rui Guo, Xiao-Jin He
Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans. Human mutation (2022)
Chunyu Liu, Ying Shen, Shuyan Tang, Jiaxiong Wang, Yiling Zhou, Shixiong Tian, Huan Wu, Jiangshan Cong, Xiao-Jin He, Li Jin, Yunxia Cao, Yihong Yang, Feng Zhang
Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility. Journal of medical genetics (2022)
Yang Gao, Liting Liu, Qunshan Shen, Feifei Fu, Chuan Xu, Hao Geng, Mingrong Lv, Kuokuo Li, Dongdong Tang, Bing Song, Huan Wu, Yuping Xu, Ying Zhang, Fangbiao Tao, Ping Zhou, Zhaolian Wei, Xiao-Jin He, Yunxia Cao
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human. Clinical genetics 102 (2) (2022)
Jiangshan Cong, Xiong Wang, Amir Amiri-Yekta, Lingbo Wang, Zine-Eddine Kherraf, Chunyu Liu, Caroline Cazin, Shuyan Tang, Seyedeh Hanieh Hosseini, Shixiong Tian, Abbas Daneshipour, Jiaxiong Wang, Yiling Zhou, Yuyan Zeng, Shenmin Yang, Xiao-Jin He, Jinsong Li, Yunxia Cao, Li Jin, Pierre F Ray, Feng Zhang
Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. Journal of medical genetics (2021)
Yang Gao, Huan Wu, Yuping Xu, Qunshan Shen, Chuan Xu, Hao Geng, Mingrong Lv, Qing Tan, Kuokuo Li, Dongdong Tang, Bing Song, Ping Zhou, Zhaolian Wei, Xiao-Jin He, Yunxia Cao
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. Human mutation 43 (3) (2021)
Huan Wu, Xin Zhang, Qunshan Shen, Yiyuan Liu, Yang Gao, Guanxiong Wang, Mingrong Lv, Rong Hua, Yuping Xu, Ping Zhou, Zhaolian Wei, Fangbiao Tao, Xiao-Jin He, Yunxia Cao, Mingxi Liu
A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia. Clinical genetics 101 (1) (2021)
Cong Ma, Huan Wu, Damin Zhu, Ying Wang, Qunshan Shen, Huiru Cheng, Junqiang Zhang, Hao Geng, Yiyuan Liu, Xiao-Jin He, Fangbiao Tao, Yunxia Cao, Xiaofeng Xu
Bi-allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport. Clinical genetics 100 (6) (2021)
Mingrong Lv, Wangjie Liu, Wangfei Chi, Xiaoqing Ni, Jiajia Wang, Huiru Cheng, Wei-Yu Li, Shenmin Yang, Huan Wu, Junqiang Zhang, Yang Gao, Chunyu Liu, Caihua Li, Chenyu Yang, Qing Tan, Dongdong Tang, Jingjing Zhang, Bing Song, Yu-Jie Chen, Qiang Li, Yading Zhong, Zhihua Zhang, Hexige Saiyin, Li Jin, Yuping Xu, Ping Zhou, Zhaolian Wei, Chuanmao Zhang, Xiao-Jin He, Feng Zhang, Yunxia Cao
Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF. Journal of medical genetics 57 (7) (2020)
Hao Geng, Dongdong Tang, Chuan Xu, Xiao-Jin He, Tingting Ye
A Novel Missense Variant of TP63 Heterozygously Present in Split-Hand/Foot Malformation. BioMed research international 2020 (2020)
Weiyu Li, Huan Wu, Fuping Li, Shixiong Tian, Zine-Eddine Kherraf, Jintao Zhang, Xiaoqing Ni, Mingrong Lv, Chunyu Liu, Qing Tan, Ying Shen, Amir Amiri-Yekta, Caroline Cazin, Jingjing Zhang, Wangjie Liu, Yan Zheng, Huiru Cheng, Yingbi Wu, Jiajia Wang, Yang Gao, Yujie Chen, Xiaomin Zha, Li Jin, Mingxi Liu, Xiao-Jin He, Pierre F Ray, Yunxia Cao, Feng Zhang
Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Journal of medical genetics 57 (2) (2019)
Chunyu Liu, Mingrong Lv, Xiao-Jin He, Yong Zhu, Amir Amiri-Yekta, Weiyu Li, Huan Wu, Zine-Eddine Kherraf, Wangjie Liu, Jingjing Zhang, Qing Tan, Shuyan Tang, Yong-Jun Zhu, Yading Zhong, Caihua Li, Shixiong Tian, Zhiguo Zhang, Li Jin, Pierre Ray, Feng Zhang, Yunxia Cao
Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility. Journal of medical genetics 57 (1) (2019)
Xiao-Jin He, Weiyu Li, Huan Wu, Mingrong Lv, Wangjie Liu, Chunyu Liu, Fuxi Zhu, Caihua Li, Youyan Fang, Chenyu Yang, Huiru Cheng, Junqiang Zhang, Jing Tan, Tingting Chen, Dongdong Tang, Bing Song, Xue Wang, Xiaomin Zha, Hongyan Wang, Zhaolian Wei, Shenmin Yang, Hexige Saiyin, Ping Zhou, Li Jin, Jian Wang, Zhiguo Zhang, Feng Zhang, Yunxia Cao
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. Journal of medical genetics 56 (2) (2018)

Xiao-Jin He.css-eqlu8i{font-size:small;padding-left:4px;} (Xiaojin He)

Publication Activity (10 Years)

Top Topics

Top Venues

Xiao-Jin He (Xiaojin He)