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Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 2, 2014
Towards understanding RNA-mediated neurological disordersRanhui Duan, Sumeet Sharma, Qiuping Xia, et al.
Journal of Child Neurology|June 26, 2014
Mutational analyses of the FMR1 gene in Chinese pediatric population of fragile x suspects: low tolerance for point mutationShiyu Luo, Wen Huang, Qiuping Xia, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|October 14, 2020
Identification of factors related to fertilization failure in in vitro fertilization-embryo transferQiuping Xia, Yanping Li, Yeqing Zhang, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese populationWen Huang, Qiuping Xia, Shiyu Luo, et al.
BMC Medical Genetics|November 26, 2014
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case reportShiyu Luo, Wen Huang, Qiuping Xia, et al.
Scientific Reports|August 20, 2025
Clinical application of nanopore sequencing for haplotype linkage analysis in preimplantation genetic testing for Duchenne muscular dystrophyQiuping Xia, Tianli Chang, Taoli Ding, et al.
Reproductive Biology and Endocrinology : RB&E|November 23, 2023
Nuclear-cytoplasmic asynchrony in oocyte maturation caused by TUBB8 variants via impairing microtubule function: a novel pathogenic mechanismTianli Chang, Jing Zhao, Qi Li, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 5, 2023
Chromosomal concordance between babies produced by the preimplantation genetic testing for aneuploidies and trophectoderm biopsies: A prospective observational studyZhongyuan Yao, Xiaoxia Wang, Jun Zeng, et al.
Journal of Ovarian Research|March 31, 2022
Mutation analysis of the TUBB8 gene in primary infertile women with oocyte maturation arrestZhongyuan Yao, Jun Zeng, Huimin Zhu, et al.
BMC Genomics|January 2, 2023
Nanopore sequencing for detecting reciprocal translocation carrier status in preimplantation genetic testingQiuping Xia, Shenglan Li, Taoli Ding, et al.
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