Min-Yue Dong (Minyue Dong, Min Chen)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 22

Top Topics

Interstitial Lung Disease

Top Venues

Molecular genetics & genomic medicine

NPJ genomic medicine

Molecular cytogenetics

Expert review of molecular diagnostics

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

Publications

Yuqing Xu, Yi Sun, Min Chen, Min-Yue Dong
A rare interstitial lung disease in children caused by novel mutations of FARSA gene. Pediatric pulmonology (2024)
Yeqing Qian, Jianjun Zhu, Zhiguo Tang, Yan Sun, Zhonghua Wang, Fei Tang, Yun Yang, Linlin Fan, Yixi Sun, Bei Liu, Min Chen, Yuqin Luo, Junjie Hu, Kai Yan, Jianfen Man, Lina Wang, Cangcang Jia, Ping Tang, Xinyi Zhu, Chaohong Wang, Junxiang Tang, Yuanyuan Xia, Xueqin Guo, Kang Zhang, Xiaoli Wang, Suping Li, Lijie Song, Jiansheng Zhu, Min-Yue Dong
Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases. Clinical and translational medicine 14 (7) (2024)
Min Chen, Mei-Hua Tan, Jiao Liu, Yan-Mei Yang, Jia-Ling Yu, Li-Juan He, Ying-Zhi Huang, Yi-Xi Sun, Ye-Qing Qian, Kai Yan, Min-Yue Dong
An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing. NPJ genomic medicine 9 (1) (2024)
Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Min-Yue Dong
Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report. Molecular genetics & genomic medicine 12 (7) (2024)
Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Min-Yue Dong
Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report. Molecular genetics & genomic medicine 12 (7) (2024)
Yuqing Xu, Ye-Qing Qian, Ying Yu, Xin Zhan, Pengzhen Jin, Jiawei Hong, Min-Yue Dong
SLC10A5 deficiency causes hypercholanemia. Hepatology (Baltimore, Md.) (2024)
Yeqing Qian, Jianjun Zhu, Zhiguo Tang, Yan Sun, Zhonghua Wang, Fei Tang, Yun Yang, Linlin Fan, Yixi Sun, Bei Liu, Min Chen, Yuqin Luo, Junjie Hu, Kai Yan, Jianfen Man, Lina Wang, Cangcang Jia, Ping Tang, Xinyi Zhu, Chaohong Wang, Junxiang Tang, Yuanyuan Xia, Xueqin Guo, Kang Zhang, Xiaoli Wang, Suping Li, Lijie Song, Jiansheng Zhu, Min-Yue Dong
Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases. Clinical and translational medicine 14 (7) (2024)
Yanfei Xu, Jianbo Lou, Yeqing Qian, Pengzhen Jin, Yangwen Qian, Jiawei Hong, Yuqing Xu, Yixuan Yin, Songjia Yi, Min-Yue Dong
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnancies. Expert review of molecular diagnostics 24 (5) (2024)
Min Chen, Mei-Hua Tan, Jiao Liu, Yan-Mei Yang, Jia-Ling Yu, Li-Juan He, Ying-Zhi Huang, Yi-Xi Sun, Ye-Qing Qian, Kai Yan, Min-Yue Dong
An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing. NPJ genomic medicine 9 (1) (2024)
Yanfei Xu, Jianbo Lou, Yeqing Qian, Pengzhen Jin, Yangwen Qian, Jiawei Hong, Yuqing Xu, Yixuan Yin, Songjia Yi, Min-Yue Dong
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnancies. Expert review of molecular diagnostics (2024)
Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Min-Yue Dong
Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report. Molecular genetics & genomic medicine 12 (7) (2024)
Yeqing Qian, Yan Sun, Xueqin Guo, Lijie Song, Yixi Sun, Xiaoyang Gao, Bei Liu, Yuqing Xu, Na Chen, Min Chen, Yuqin Luo, Zhihong Qiao, Linlin Fan, Jianfen Man, Kang Zhang, Xiaoli Wang, Tingting Rong, Zhonghua Wang, Fengxia Liu, Jing Zhao, Xiaoming Wei, Minfeng Chen, Zhiyu Peng, Huanhuan Peng, Jun Sun, Min-Yue Dong
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples. Journal of medical genetics (2023)
Jingjin Yang, Yuxin Liu, Min-Yue Dong
Integrated Bioinformatics Analysis to Screen Hub Gene Signatures for Fetal Growth Restriction. Genetics research 2023 (2023)
Kai Yan, Jiahui Zhang, Pui Y Lee, Panfeng Tao, Jun Wang, Shihao Wang, Qing Zhou, Min-Yue Dong
Haploinsufficiency of PSMD12 Causes Proteasome Dysfunction and Subclinical Autoinflammation. Arthritis & rheumatology (Hoboken, N.J.) 74 (6) (2022)
Hui Zhu, Xiaoxiao Jin, Yuqing Xu, Weihua Zhang, Xiaodan Liu, Jinglei Jin, Yeqing Qian, Min-Yue Dong
Efficiency of non-invasive prenatal screening in pregnant women at advanced maternal age. BMC pregnancy and childbirth 21 (1) (2021)
Yixi Sun, Yali Yang, Yuqin Luo, Min Chen, Liya Wang, Yingzhi Huang, Yanmei Yang, Min-Yue Dong
Lack of MECP2 gene transcription on the duplicated alleles of two related asymptomatic females with Xq28 duplications and opposite X-chromosome inactivation skewing. Human mutation 42 (11) (2021)
Yeqing Qian, Gang Hu, Min Chen, Bei Liu, Kai Yan, Caiyun Zhou, Yanqin Yu, Min-Yue Dong
Novel deep intronic and frameshift mutations causing a TRIP11-related disorder. American journal of medical genetics. Part A 185 (8) (2021)
Min-Yue Dong, Min Zhang, Ye-Qing Qian, Yanmei Yang, Yixi Sun, Bei Liu, Liya Wang, Minyue Dong
Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping. NPJ genomic medicine 5 (2020)
Yuqin Luo, Bei Jia, Kai Yan, Siping Liu, Xiaojie Song, Mingfa Chen, Fan Jin, Yang Du, Juan Wang, Yan Hong, Sha Cao, Dawei Li, Min-Yue Dong
Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single-gene disorder screening. Molecular genetics & genomic medicine 7 (4) (2019)
Li-Ya Wang, Xing-Qiang Rao, Yu-Qin Luo, Bei Liu, Chun-Fang Peng, Dan Chen, Kai Yan, Ye-Qing Qian, Yan-Mei Yang, Ying-Zhi Huang, Min Chen, Yi-Xi Sun, Hong-Ge Li, Ying-Hui Ye, Fan Jin, Hai-Liang Liu, Min-Yue Dong
Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform. Human genomics 13 (1) (2019)
Hongge Li, Yu Lei, Hui Zhu, Yuqin Luo, Yeqing Qian, Min Chen, Yixi Sun, Kai Yan, Yanmei Yang, Bei Liu, Liya Wang, Yingzhi Huang, Junjie Hu, Jianyun Xu, Min-Yue Dong
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies. Molecular cytogenetics 11 (2018)
Ye-Qing Qian, Xiao-Ying Fu, Xiao-Qing Wang, Yu-Qin Luo, Min Chen, Kai Yan, Yan-Mei Yang, Bei Liu, Li-Ya Wang, Ying-Zhi Huang, Hong-Ge Li, Hang-Yi Pan, Fan Jin, Min-Yue Dong
A feasible diagnostic approach for the translocation carrier from the indication of products of conception. Molecular cytogenetics 11 (2018)