Huijun Wang

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 19

Top Venues

Molecular genetics & genomic medicine

Journal of medical genetics

NPJ genomic medicine

Archives of disease in childhood. Fetal and neonatal edition

Fudan University (PHD)

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

Education History

Fudan University Sep 01 1998 - Jun 30 2001

China

PHD :: Pathology

Tongji Medical College Sep 01 1987 - Jun 30 1992

China

BSC

Publications

Yinmo Jiang, Bingbing Wu, Xi Zhang, Lin Yang, Sujuan Wang, Huiping Li, Shuizhen Zhou, Yanyan Qian, Huijun Wang
Thirteen New Patients of PPP2R5D Gene Mutation and the Fine Profile of Genotype-Phenotype Correlation Unraveling the Pathogenic Mechanism Underlying Macrocephaly Phenotype. Children (Basel, Switzerland) 11 (8) (2024)
Qiufang Guo, Ping Zhang, Wenjing Ying, Yaqiong Wang, Jitao Zhu, Gang Li, Huijun Wang, Xiaochuan Wang, Caixia Lei, Wen-Hao Zhou, Jinqiao Sun, Bingbing Wu
Intron retention by a novel intronic mutation in DKC1 gene caused recurrent still birth and early death in a Chinese family. Molecular genetics & genomic medicine 10 (6) (2022)
Ping Zhang, Bingbing Wu, Yaqiong Wang, Yunyun Ren, Gang Li, Yanyan Qan, Caixia Lei, Huijun Wang
Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family. Reproductive sciences (Thousand Oaks, Calif.) 29 (8) (2022)
Yunqian Zhu, Xiaonan Du, Li Sun, Huijun Wang, Dahui Wang, Bingbing Wu
Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review. Molecular genetics & genomic medicine 10 (8) (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)
Huijun Wang, Feifan Xiao, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Wei Lu, 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, Yanyan Qian, Xu Li, Xiaomin Peng, Yao Wang, Fang Liu, Dahui Wang, Hao Li, Chun Shen, Liling Qian, Yun Cao, Bingbing Wu, Wen-Hao Zhou
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project. Human mutation 42 (4) (2021)
Yanyan Qian, Yuanfeng Zhou, Bingbing Wu, Huiyao Chen, Suzhen Xu, Yao Wang, Ping Zhang, Gang Li, Qiong Xu, Wenhao Zhou, Xiu Xu, Huijun Wang
Novel Variants of the SMARCA4 Gene Associated with Autistic Features Rather Than Typical Coffin-Siris Syndrome in Eight Chinese Pediatric Patients. Journal of autism and developmental disorders (2021)
Dan Dai, Mei Mei, Liyuan Hu, Yun Cao, Xiaochuan Wang, Libo Wang, Yulan Lu, Lin Yang, Xinran Dong, Huijun Wang, Bingbing Wu, Liling Qian
Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype. Archives of disease in childhood (2021)
Sha Yu, Wen-Xia Chen, Wei Lu, Chao Chen, Yihua Ni, Bo Duan, Bin Wang, Huijun Wang, Zheng-Min Xu
Novel heterozygous GATA3 and SLC34A3 variants in a 6-year-old boy with Barakat syndrome and hypercalciuria. Molecular genetics & genomic medicine 8 (5) (2020)
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)
Yanyan Qian, Bingbing Wu, Yulan Lu, Wenhao Zhou, Sujuan Wang, Huijun Wang
Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report. BMC medical genetics 21 (1) (2020)
Xinran Dong, Bo Liu, Lin Yang, Huijun Wang, Bingbing Wu, Renchao Liu, Hongbo Chen, Xiang Chen, Sha Yu, Bin Chen, Sujuan Wang, Xiu Xu, Wenhao Zhou, Yulan Lu
Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort. Journal of medical genetics 57 (8) (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)
Sha Yu, Bingbing Wu, Yanyan Qian, Ping Zhang, Yulan Lu, Xinran Dong, Qing Wang, Xuemei Zhao, Renchao Liu, Wenhao Zhou, Huijun Wang
Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein-Taybi Syndrome kids with high frequency of polydactyly. Molecular genetics & genomic medicine 7 (12) (2019)
Lin Yang, Xu Liu, Zixiu Li, Peng Zhang, Bingbing Wu, Huijun Wang, Liyuan Hu, Guoqiang Cheng, Laishuan Wang, Wenhao Zhou
Genetic aetiology of early infant deaths in a neonatal intensive care unit. Journal of medical genetics 57 (3) (2019)
Yanyan Qian, Bingbing Wu, Yulan Lu, Xinran Dong, Qian Qin, Wenhao Zhou, Huijun Wang
Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation. Cold Spring Harbor molecular case studies 4 (6) (2018)

Huijun Wang.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Huijun Wang