Wen-Hao Zhou (Wenhao Zhou)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 36

Top Venues

Nature communications

World journal of pediatrics : WJP

Cell discovery

Molecular genetics & genomic medicine

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

Publications

Elina Idiiatullina, Mahmoud Al-Azab, Meng Lin, Katja Hrovat-Schaale, Ziyang Liu, Xiaotian Li, Caiqin Guo, Xixi Chen, Yaoying Li, Song Gao, Jun Cui, Wen-Hao Zhou, Li Liu, Yuxia Zhang, Seth L Masters
Heterozygous de novo dominant negative mutation of REXO2 results in interferonopathy. Nature communications 15 (1) (2024)
Fuqiang Yang, Ziqi Zhao, Dan Zhang, Yu Xiong, Xinran Dong, Yuchen Wang, Min Yang, Taotao Pan, Chuanyu Liu, Kaiyi Liu, Yifeng Lin, Yongjie Liu, Qiang Tu, Yashan Dang, Mingyang Xia, Da Mi, Wen-Hao Zhou, Zhiheng Xu
Single-cell multi-omics analysis of lineage development and spatial organization in the human fetal cerebellum. Cell discovery 10 (1) (2024)
Elina Idiiatullina, Mahmoud Al-Azab, Meng Lin, Katja Hrovat-Schaale, Ziyang Liu, Xiaotian Li, Caiqin Guo, Xixi Chen, Yaoying Li, Song Gao, Jun Cui, Wen-Hao Zhou, Li Liu, Yuxia Zhang, Seth L Masters
Heterozygous de novo dominant negative mutation of REXO2 results in interferonopathy. Nature communications 15 (1) (2024)
Fuqiang Yang, Ziqi Zhao, Dan Zhang, Yu Xiong, Xinran Dong, Yuchen Wang, Min Yang, Taotao Pan, Chuanyu Liu, Kaiyi Liu, Yifeng Lin, Yongjie Liu, Qiang Tu, Yashan Dang, Mingyang Xia, Da Mi, Wen-Hao Zhou, Zhiheng Xu
Single-cell multi-omics analysis of lineage development and spatial organization in the human fetal cerebellum. Cell discovery 10 (1) (2024)
Kai Yan, Lu-Kun Tang, Fei-Fan Xiao, Peng Zhang, Guo-Qiang Cheng, Lai-Shuan Wang, Chun-Mei Lu, Meng-Meng Ge, Li-Yuan Hu, Yuan-Feng Zhou, Tian-Tian Xiao, Yan Xu, Zhao-Qing Yin, Gang-Feng Yan, Guo-Ping Lu, Qi Li, Wen-Hao Zhou
Brain development in newborns and infants after ECMO. World journal of pediatrics : WJP 20 (6) (2024)
Fuqiang Yang, Ziqi Zhao, Dan Zhang, Yu Xiong, Xinran Dong, Yuchen Wang, Min Yang, Taotao Pan, Chuanyu Liu, Kaiyi Liu, Yifeng Lin, Yongjie Liu, Qiang Tu, Yashan Dang, Mingyang Xia, Da Mi, Wen-Hao Zhou, Zhiheng Xu
Single-cell multi-omics analysis of lineage development and spatial organization in the human fetal cerebellum. Cell discovery 10 (1) (2024)
Kai Yan, Lu-Kun Tang, Fei-Fan Xiao, Peng Zhang, Guo-Qiang Cheng, Lai-Shuan Wang, Chun-Mei Lu, Meng-Meng Ge, Li-Yuan Hu, Yuan-Feng Zhou, Tian-Tian Xiao, Yan Xu, Zhao-Qing Yin, Gang-Feng Yan, Guo-Ping Lu, Qi Li, Wen-Hao Zhou
Brain development in newborns and infants after ECMO. World journal of pediatrics : WJP 20 (6) (2024)
Elina Idiiatullina, Mahmoud Al-Azab, Meng Lin, Katja Hrovat-Schaale, Ziyang Liu, Xiaotian Li, Caiqin Guo, Xixi Chen, Yaoying Li, Song Gao, Jun Cui, Wen-Hao Zhou, Li Liu, Yuxia Zhang, Seth L Masters
Heterozygous de novo dominant negative mutation of REXO2 results in interferonopathy. Nature communications 15 (1) (2024)
Kai Yan, Lu-Kun Tang, Fei-Fan Xiao, Peng Zhang, Guo-Qiang Cheng, Lai-Shuan Wang, Chun-Mei Lu, Meng-Meng Ge, Li-Yuan Hu, Yuan-Feng Zhou, Tian-Tian Xiao, Yan Xu, Zhao-Qing Yin, Gang-Feng Yan, Guo-Ping Lu, Qi Li, Wen-Hao Zhou
Brain development in newborns and infants after ECMO. World journal of pediatrics : WJP (2024)
Chuchu Fang, Wen-Hao Zhou
Genetic background of neonatal hypokalemia. Pediatric nephrology (Berlin, Germany) (2024)
Kai Yan, Lu-Kun Tang, Fei-Fan Xiao, Peng Zhang, Guo-Qiang Cheng, Lai-Shuan Wang, Chun-Mei Lu, Meng-Meng Ge, Li-Yuan Hu, Yuan-Feng Zhou, Tian-Tian Xiao, Yan Xu, Zhao-Qing Yin, Gang-Feng Yan, Guo-Ping Lu, Qi Li, Wen-Hao Zhou
Brain development in newborns and infants after ECMO. World journal of pediatrics : WJP 20 (6) (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Ping Cheng, Aimin Qian, Hongbo Zhang, Yingying Wang, Shujuan Li, Mengya Sun, Jie Yang, Jianguo Zhou, Li-Yuan Hu, Xiaoping Lei, Yu Hu, Ligang Zhou, Lizhong Du, Yun Cao, Shoo K Lee, Wen-Hao Zhou, Wenqing Kang, Changlian Zhu, Huiqing Sun, Siyuan Jiang
Epidemiology, microbiology and antibiotic treatment of bacterial and fungal meningitis among very preterm infants in China: a cross-sectional study. Archives of disease in childhood. Fetal and neonatal edition (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Elina Idiiatullina, Mahmoud Al-Azab, Meng Lin, Katja Hrovat-Schaale, Ziyang Liu, Xiaotian Li, Caiqin Guo, Xixi Chen, Yaoying Li, Song Gao, Jun Cui, Wen-Hao Zhou, Li Liu, Yuxia Zhang, Seth L Masters
Heterozygous de novo dominant negative mutation of REXO2 results in interferonopathy. Nature communications 15 (1) (2024)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
Hui Xiao, Huiyao Chen, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Yun Cao, Liyuan Hu, Xinran Dong, Wen-Hao Zhou, Lin Yang
Comprehensive assessment of the genetic characteristics of small for gestational age newborns in NICU: from diagnosis of genetic disorders to prediction of prognosis. Genome medicine 15 (1) (2023)
Wangpeng Gu, Jia Zhang, Qing Li, Yaguang Zhang, Xuan Lin, Bingbing Wu, Qi Yin, Jinqiao Sun, Yulan Lu, Xiaoyu Sun, Caiwei Jia, Chuanyin Li, Yu Zhang, Meng Wang, Xidi Yin, Su Wang, Jiefang Xu, Ran Wang, Songling Zhu, Shipeng Cheng, Shuangfeng Chen, Lian Liu, Lin Zhu, Chenghua Yan, Chunyan Yi, Xuezhen Li, Qiaoshi Lian, Guomei Lin, Zhiyang Ling, Liyan Ma, Min Zhou, Kuanlin Xiao, Haiming Wei, Ronggui Hu, Wen-Hao Zhou, Lilin Ye, Hai-Kun Wang, Jinsong Li, Bing Sun
The TRIM37 variants in Mulibrey nanism patients paralyze follicular helper T cell differentiation. Cell discovery 9 (1) (2023)
Yu-Xi Chen, Tian-Tian Xiao, Hui-Yao Chen, Xiang Chen, Ya-Qiong Wang, Qi Ni, Bing-Bing Wu, Hui-Jun Wang, Yu-Lan Lu, Li-Yuan Hu, Yun Cao, Guo-Qiang Cheng, Lai-Shuan Wang, Fei-Fan Xiao, Lin Yang, Xin-Ran Dong, Wen-Hao Zhou
Risk stratification of hemodynamically significant patent ductus arteriosus by clinical and genetic factors. World journal of pediatrics : WJP (2023)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
James T Morton, Dong-Min Jin, Robert H Mills, Yan Shao, Gibraan Rahman, Daniel McDonald, Qiyun Zhu, Metin Balaban, Yueyu Jiang, Kalen Cantrell, Antonio Gonzalez, Julie Carmel, Linoy Mia Frankiensztajn, Sandra Martin-Brevet, Kirsten Berding, Brittany D Needham, María Fernanda Zurita, Maude David, Olga V Averina, Alexey S Kovtun, Antonio Noto, Michele Mussap, Mingbang Wang, Daniel N Frank, Ellen Li, Wen-Hao Zhou, Vassilios Fanos, Valery N Danilenko, Dennis Paul Wall, Paúl Andrés Cárdenas, Manuel E Baldeón, Sebastien Jacquemont, Omry Koren, Evan Elliott, Ramnik J Xavier, Sarkis K Mazmanian, Rob Knight, Jack A Gilbert, Sharon M Donovan, Trevor D Lawley, Bob Carpenter, Richard Bonneau, Gaspar Taroncher-Oldenburg
Multi-level analysis of the gut-brain axis shows autism spectrum disorder-associated molecular and microbial profiles. Nature neuroscience (2023)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
Zaili Luo, Dazhuan Xin, Yunfei Liao, Kalen Berry, Sean Ogurek, Feng Zhang, Liguo Zhang, Chuntao Zhao, Rohit Rao, Xinran Dong, Hao Li, Jianzhong Yu, Yifeng Lin, Guoying Huang, Lingli Xu, Mei Xin, Ryuichi Nishinakamura, Jiyang Yu, Marcel Kool, Stefan M Pfister, Martine F Roussel, Wen-Hao Zhou, William A Weiss, Paul R Andreassen, Qing Richard Lu
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability. Nature communications 14 (1) (2023)
Zaili Luo, Mingyang Xia, Wei Shi, Chuntao Zhao, Jiajia Wang, Dazhuan Xin, Xinran Dong, Yu Xiong, Feng Zhang, Kalen Berry, Sean Ogurek, Xuezhao Liu, Rohit Rao, Rui Xing, Lai Man Natalie Wu, Siying Cui, Lingli Xu, Yifeng Lin, Wenkun Ma, Shuaiwei Tian, Qi Xie, Li Zhang, Mei Xin, Xiao-Tao Wang, Feng Yue, Haizi Zheng, Yaping Liu, Charles B Stevenson, Peter M K de Blank, John P Perentesis, Richard J Gilbertson, Hao Li, Jie Ma, Wen-Hao Zhou, Michael D Taylor, Qing Richard Lu
Human fetal cerebellar cell atlas informs medulloblastoma origin and oncogenesis. Nature (2022)
Kai Yan, Lu-Kun Tang, Fei-Fan Xiao, Peng Zhang, Chun-Mei Lu, Li-Yuan Hu, Lai-Shuan Wang, Guo-Qiang Cheng, Wen-Hao Zhou
Monkeypox and the perinatal period: what does maternal-fetal medicine need to know? World journal of pediatrics : WJP (2022)
Yunfei Liao, Zaili Luo, Yifeng Lin, Huiyao Chen, Tong Chen, Lingli Xu, Sean Orgurek, Kalen Berry, Monika Dzieciatkowska, Julie A Reisz, Angelo D'Alessandro, Wen-Hao Zhou, Qing Richard Lu
PRMT3 drives glioblastoma progression by enhancing HIF1A and glycolytic metabolism. Cell death & disease 13 (11) (2022)
Huijun Wang, Feifan Xiao, Yanyan Qian, Bingbing Wu, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Kai Yan, Lin Yang, Liping Chen, Wenqing Kang, Long Li, Xinnian Pan, Qiufen Wei, Deyi Zhuang, Dongmei Chen, Zhaoqing Yin, Ling Yang, Qi Ni, Renchao Liu, Gang Li, Ping Zhang, Xu Li, Xiaomin Peng, Yao Wang, Huiyao Chen, Xiaojing Ma, Fang Liu, Yun Cao, Guoying Huang, Wen-Hao Zhou
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project. Journal of medical genetics (2022)
Tiantian Xiao, Jin Wang, Huijun Wang, Hongfang Mei, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Li-Yuan Hu, Wei Lu, Qi Ni, Gang Li, Ping Zhang, Yanyan Qian, Xu Li, Xiaomin Peng, Yao Wang, Chun Shen, Gong Chen, Ya-Lan Dou, Yun Cao, Liping Chen, Wenqing Kang, Long Li, Xinnian Pan, Qiufen Wei, Deyi Zhuang, Dong-Mei Chen, Zhaoqing Yin, Jianshe Wang, Lin Yang, Bingbing Wu, Wen-Hao Zhou
Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome Project. Archives of disease in childhood. Fetal and neonatal edition (2022)
Lin Yang, Zejun Wei, Xiang Chen, Liyuan Hu, Xiaomin Peng, Jin Wang, Chunmei Lu, Yanting Kong, Xinran Dong, Qi Ni, Yulan Lu, Bingbing Wu, Huijun Wang, Katia Meirelles, Xia Tian, Jing Zhang, Fengqi Chang, Liu Liu, Changhua Li, Wesley You, Guoqiang Cheng, Laishuan Wang, Yun Cao, Chao Chen, Ping Fang, Sha Tang, Wen-Hao Zhou
Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China. Clinical genetics 101 (1) (2021)
Ping Zhang, Bingbing Wu, Yulan Lu, Qi Ni, Renchao Liu, Wen-Hao Zhou, Huijun Wang
First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant. Molecular genetics & genomic medicine 8 (3) (2020)
Xiaoxiang Song, Xiaoyan Fang, Xiaoshan Tang, Qi Cao, Yihui Zhai, Jing Chen, Jialu Liu, Zhiqing Zhang, Tianchao Xiang, Yanyan Qian, Bingbing Wu, Huijun Wang, Wen-Hao Zhou, Cuihua Liu, Qian Shen, Hong Xu, Jia Rao
COQ8B nephropathy: Early detection and optimal treatment. Molecular genetics & genomic medicine 8 (8) (2020)
Huijun Wang, Yanyan Qian, Yulan Lu, Qian Qin, Guoping Lu, Guoqiang Cheng, Ping Zhang, Lin Yang, Bingbing Wu, Wen-Hao Zhou
Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants. NPJ genomic medicine 5 (2020)
Lin Yang, Zixiu Li, Mei Mei, Xiaomei Fan, Guodong Zhan, Huijun Wang, Guoying Huang, Mingbang Wang, Weidong Tian, Wen-Hao Zhou
Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alström syndrome. BMC medical genetics 18 (1) (2017)

Wen-Hao Zhou.css-eqlu8i{font-size:small;padding-left:4px;} (Wenhao Zhou)

Publication Activity (10 Years)

Top Topics

Top Venues

Wen-Hao Zhou (Wenhao Zhou)