Lingqian Wu

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 12

Top Topics

Dna Methylation

Top Venues

Molecular genetics & genomic medicine

Journal of human genetics

Clinical genetics

Human reproduction (Oxford, England)

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

Publications

Li-Ying Yan, Yunxia Cao, Zi-Jiang Chen, Jie Du, ShuYu Wang, Hefeng Huang, Jin Huang, Rong Li, Ping Liu, Zhe Zhang, Yu Huang, Ge Lin, Hong Pan, Hongbo Qi, Weiping Qian, Yun Sun, Lingqian Wu, Yuanqing Yao, Bo Zhang, Cuilian Zhang, Shuyun Zhao, Canquan Zhou, Xue Zhang, Jie Qiao
Chinese experts' consensus guideline on preimplantation genetic testing of monogenic disorders. Human reproduction (Oxford, England) 38 (Supplement_2) (2023)
Li Zhang, Lijuan Pan, Yanling Teng, Desheng Liang, Zhuo Li, Lingqian Wu
Molecular diagnosis for 55 fetuses with skeletal dysplasias by whole-exome sequencing: A retrospective cohort study. Clinical genetics 100 (2) (2021)
Lanlan Zeng, Zhibin Li, Lijuan Pan, Hongyan Li, Jiayu Wu, Xiying Yuan, Zhuo Li, Desheng Liang, Lingqian Wu
Novel GZF1 pathogenic variants identified in two Chinese patients with Larsen syndrome. Clinical genetics 99 (2) (2020)
Jianyan Pan, Chunhua Zhang, Yanling Teng, Sijing Zeng, Siyi Chen, Desheng Liang, Zhuo Li, Lingqian Wu
Detection of Spinal Muscular Atrophy Using a Duplexed Real-Time PCR Approach With Locked Nucleic Acid-Modified Primers. Annals of laboratory medicine 41 (1) (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)
Mengmeng Liu, Yunshan Zhong, Hongqian Liu, Desheng Liang, Erhong Liu, Yu Zhang, Feng Tian, Qiaowei Liang, David S Cram, Hua Wang, Lingqian Wu, Fuli Yu
REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis. Molecular genetics & genomic medicine 8 (11) (2020)
Ming Lei, Desheng Liang, Yifeng Yang, Satomi Mitsuhashi, Kazutaka Katoh, Noriko Miyake, Martin C Frith, Lingqian Wu, Naomichi Matsumoto
Long-read DNA sequencing fully characterized chromothripsis in a patient with Langer-Giedion syndrome and Cornelia de Lange syndrome-4. Journal of human genetics 65 (8) (2020)
Yingdi Liu, Jinjie Xue, Zhuo Li, Siyuan Linpeng, Hu Tan, Yanling Teng, Desheng Liang, Lingqian Wu
A novel GJB1 mutation associated with X-linked Charcot-Marie-Tooth disease in a large Chinese family pedigree. Molecular genetics & genomic medicine 8 (3) (2020)
Ming Lei, Satomi Mitsuhashi, Noriko Miyake, Tohru Ohta, Desheng Liang, Lingqian Wu, Naomichi Matsumoto
Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome. Journal of human genetics 64 (7) (2019)
Hui Tang, Jing Guo, Siyuan Linpeng, Lingqian Wu
Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese children. Orphanet journal of rare diseases 14 (1) (2019)
Yanghui Zhang, Haoxian Li, Jing Liu, Huiming Yan, Qin Liu, Xianda Wei, Hui Xi, Zhengjun Jia, Lingqian Wu, Hua Wang
Molecular investigation in Chinese patients with primary carnitine deficiency. Molecular genetics & genomic medicine 7 (9) (2019)
Siyuan Linpeng, Jing Liu, Jianyan Pan, Yingxi Cao, Yanling Teng, Desheng Liang, Zhuo Li, Lingqian Wu
Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1. BioMed research international 2018 (2018)