Ying Peng

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 6

Top Topics

Dna Methylation

Genome Wide Identification

Top Venues

Molecular genetics & genomic medicine

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

Publications

Ying Peng, Shuting Yang, Hui Xi, Jiancheng Hu, Zhengjun Jia, Jialun Pang, Jing Liu, Wenxian Yu, Chengyuan Tang, Hua Wang
Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family. Molecular genetics & genomic medicine 9 (3) (2021)
Hui Xi, Wanqin Xie, Jing Chen, Wanglan Tang, Xiuli Deng, Hua Li, Ying Peng, Dan Wang, Shuting Yang, Yanan Zhang, Ranhui Duan, Junqun Fang, Hua Wang
Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center. Molecular genetics & genomic medicine 9 (7) (2021)
Na Ma, Zhenhua Zhu, Jing Liu, Ying Peng, Xiaomeng Zhao, Weiling Tang, Zhengjun Jia, Hui Xi, Bodi Gao, Hua Wang, Juan Du
Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by synonymous mutation in COL5A2. Molecular genetics & genomic medicine 9 (5) (2021)
Jing Liu, Qin Liu, Shuting Yang, Na Ma, Jialun Pang, Ying Peng, Hui Xi, Zhengjun Jia, Yingchun Luo, Meiping Jiang, Yanling Teng, Wenxian Yu, Zhuo Li, Hua Wang
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review. Molecular genetics & genomic medicine 9 (8) (2021)
Ying Peng, Jialun Pang, Jiancheng Hu, Zhengjun Jia, Hui Xi, Na Ma, Shuting Yang, Jing Liu, Xiaoliang Huang, Chengyuan Tang, Hua Wang
Clinical and molecular characterization of 12 prenatal cases of Cri-du-chat syndrome. Molecular genetics & genomic medicine 8 (8) (2020)
Jing Liu, Pengsiyuan Lin, Jialun Pang, Zhengjun Jia, Ying Peng, Hui Xi, Lingqian Wu, Zhuo Li, Hua Wang
Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome. Molecular genetics & genomic medicine 8 (8) (2020)