Ruizhi Liu

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Intellectual Disability

Top Venues

Journal of clinical laboratory analysis

BioMed research international

Molecular genetics & genomic medicine

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

Publications

Tangfei Xu, Fagui Yue, Jing He, Hongguo Zhang, Ruizhi Liu
Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review. Medicine 103 (30) (2024)
Tangfei Xu, Fagui Yue, Jing He, Hongguo Zhang, Ruizhi Liu
Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review. Medicine 103 (30) (2024)
Xinyue Zhang, Fagui Yue, Qingyang Shi, Yuting Jiang, Jing He, Leilei Li, Ruizhi Liu
Prenatal detection and molecular cytogenetic characterization of 19q13.42 microduplication: three reported cases and literature review. Molecular cytogenetics 14 (1) (2021)
Xiaonan Hu, Leilei Li, Hongguo Zhang, Zhuming Hu, Linlin Li, Meiling Sun, Ruizhi Liu
Prenatal diagnosis of a de novo tetrasomy 15q24.3-25.3: Case report and literature review. Journal of clinical laboratory analysis 34 (7) (2020)
Shuang Chen, Qi Xi, Xinyue Zhang, Yuting Jiang, Leilei Li, Ruizhi Liu, Hongguo Zhang
Molecular cytogenetic studies of a male carrier with a unique (Y;14) translocation: Case report. Journal of clinical laboratory analysis 35 (2) (2020)
Linlin Li, Xinyue Zhang, Qingyang Shi, Leilei Li, Yuting Jiang, Ruizhi Liu, Hongguo Zhang
Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature. Journal of clinical laboratory analysis 35 (1) (2020)
Leilei Li, Ruixue Wang, Yang Yu, Hongguo Zhang, Yuting Jiang, Xiao Yang, Ruizhi Liu
CHD7 missense variants and clinical characteristics of Chinese males with infertility. Molecular genetics & genomic medicine 8 (9) (2020)
Han Zhang, Qi Xi, Xiangyin Liu, Fagui Yue, Hongguo Zhang, Meiling Sun, Ruizhi Liu
Prenatal Diagnosis and Molecular Cytogenetic Characterization of Copy Number Variations on 4p15.2p16.3, Xp22.31, and 12p11.1q11 in a Fetus with Ultrasound Anomalies: A Case Report and Literature Review. BioMed research international 2020 (2020)
Yuting Jiang, Yang Yu, Han Zhang, Hongguo Zhang, Meiling Sun, Ruizhi Liu
Xp;Yq Unbalanced Translocation with Pseudoautosomal Region Aberrations in a Natural Two-Generation Transmission. BioMed research international 2020 (2020)
MengZhe Hao, LeiLei Li, Han Zhang, LinLin Li, Ruizhi Liu, Yang Yu
The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis. Journal of clinical laboratory analysis 34 (12) (2020)
Leilei Li, Han Zhang, Yi Yang, Hongguo Zhang, Ruixue Wang, Yuting Jiang, Ruizhi Liu
High frequency of Y chromosome microdeletions in male infertility patients with 45,X/46,XY mosaicism. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 53 (3) (2020)
Dongliang Zhu, Hongguo Zhang, Ruixue Wang, Xiaojun Liu, Yuting Jiang, Tao Feng, Ruizhi Liu, Guirong Zhang
Association of DNAH11 gene polymorphisms with asthenozoospermia in Northeast Chinese patients. Bioscience reports 39 (6) (2019)
Na An, Yang Yu, Qi Xi, Fagui Yue, Ruizhi Liu, Shibo Li, Ruixue Wang
Molecular Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Chromosome Y in an Infertile Male with Apparently Normal Phenotype: A Case Report and Literature Review. BioMed research international 2019 (2019)
Dongfeng Geng, Hongguo Zhang, Xiangyin Liu, Jia Fei, Yuting Jiang, Ruizhi Liu, Ruixue Wang, Guirong Zhang
Identification of KISS1R gene mutations in disorders of non-obstructive azoospermia in the northeast population of China. Journal of clinical laboratory analysis 34 (4) (2019)
Leilei Li, Xiao Yang, Ruixue Wang, Xiaojun Liu, Yang Yu, Tao Feng, Ruizhi Liu, Guirong Zhang
Androgen receptor gene mutations are associated with male infertility in Northeast China: Clinical features and identification of two novel mutations. Andrologia 51 (3) (2018)
Dongfeng Geng, Xiao Yang, Ruixue Wang, Shu Deng, Leilei Li, Xiaonan Hu, Yuting Jiang, Ruizhi Liu
A novel stopgain mutation c.G992A (p.W331X) in TACR3 gene was identified in nonobstructive azoospermia by targeted next-generation sequencing. Journal of clinical laboratory analysis 33 (3) (2018)