Shanling Liu

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 22

Top Topics

Pregnancy Outcomes

Top Venues

Prenatal diagnosis

Clinical genetics

BioMed research international

Analytical methods : advancing methods and applications

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

Publications

Ping Wang, Hong Liao, Quyou Wang, Hanbing Xie, Bocheng Xu, Qinqin Xiang, He Wang, Mei Yang, Shanling Liu
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinism. Clinical genetics 105 (5) (2024)
Ping Wang, Hong Liao, Quyou Wang, Hanbing Xie, Bocheng Xu, Qinqin Xiang, He Wang, Mei Yang, Shanling Liu
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinism. Clinical genetics (2024)
Ping Wang, Hong Liao, Quyou Wang, Hanbing Xie, Bocheng Xu, Qinqin Xiang, He Wang, Mei Yang, Shanling Liu
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinism. Clinical genetics 105 (5) (2024)
Xijing Liu, Zhu Zhang, Xuan Zhang, Jiamin Wang, Jieni Jiang, Lingping Li, He Wang, Shanling Liu, Ting Hu
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases. Prenatal diagnosis (2024)
Jun Ren, Cuiting Peng, Han Chen, Fan Zhou, Yuezhi Keqie, Yutong Li, Hong Yang, Haixia Zhang, Ze Du, Ting Hu, Xuemei Zhang, Shan Luo, Wei Fan, Yan Wang, He Wang, Xinlian Chen, Shanling Liu
Asian Screening Array and Next-Generation Sequencing Based Panels Applied to Preimplantation Genetic Testing for Monogenic Disorders Preclinical Workup in 294 Families: A Retrospective Analysis. Prenatal diagnosis (2024)
Xijing Liu, Zhu Zhang, Xuan Zhang, Jiamin Wang, Jieni Jiang, Lingping Li, He Wang, Shanling Liu, Ting Hu
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases. Prenatal diagnosis 44 (5) (2024)
Wei Luo, Bin He, Daiwen Han, Lixing Yuan, Jun Tang, Ling Pang, Kai Zhao, Fene Zou, Ting Hu, Shanling Liu
Improved contingent screening strategy increased trisomy 21 detection rate in the second trimester. Archives of gynecology and obstetrics (2024)
Ping Wang, Hong Liao, Quyou Wang, Hanbing Xie, Bocheng Xu, Qinqin Xiang, He Wang, Mei Yang, Shanling Liu
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinism. Clinical genetics 105 (5) (2024)
Xijing Liu, Zhu Zhang, Xuan Zhang, Jiamin Wang, Jieni Jiang, Lingping Li, He Wang, Shanling Liu, Ting Hu
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases. Prenatal diagnosis 44 (5) (2024)
Xijing Liu, Zhu Zhang, Xuan Zhang, Jiamin Wang, Jieni Jiang, Lingping Li, He Wang, Shanling Liu, Ting Hu
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases. Prenatal diagnosis 44 (5) (2024)
Yanping Qian, Like Xiao, Lijuan Zhang, Ting Hu, Jiamin Wang, Rui Hu, Na Liao, Zhushu Liu, He Wang, Shanling Liu, Zhu Zhang
Prenatal diagnosis with chromosome microarray and pregnancy outcomes of fetuses with biliary tract system abnormalities. Prenatal diagnosis 42 (11) (2022)
Juan Zou, Ying He, Huiling Chen, Peng Wang, Xue Xiao, Shanling Liu
A Clinicopathologic Analysis of Decidual Polyps: A Potentially Problematic Diagnosis. International journal of clinical practice 2022 (2022)
Xiaofeng Tang, Qiaolin Li, Juan Wang, Shanling Liu
An exonuclease III-amplified 4-way strand migration system for low-abundance deletion mutation. Analytical methods : advancing methods and applications 14 (43) (2022)
Ping Wang, Hong Liao, Quyou Wang, Hanbing Xie, He Wang, Mei Yang, Shanling Liu
L1 Syndrome Prenatal Diagnosis Supplemented by Functional Analysis of One L1CAM Gene Missense Variant. Reproductive sciences (Thousand Oaks, Calif.) 29 (3) (2021)
Mei Yang, Hanbing Xie, Bocheng Xu, Qinqin Xiang, He Wang, Ting Hu, Shanling Liu
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing. Journal of clinical laboratory analysis 35 (9) (2021)
Lan Liu, Yongcang Zhang, Liang Tang, Hua Zhong, Dunzhu Danzeng, Cuiting Liang, Shanling Liu
The Neuroprotective Effect of Byu d Mar 25 in LPS-Induced Alzheimer's Disease Mice Model. Evidence-based complementary and alternative medicine : eCAM 2021 (2021)
Zhu Zhang, Ting Hu, Jiamin Wang, Rui Hu, Qinqin Li, Like Xiao, Na Liao, Zhushu Liu, He Wang, Shanling Liu
Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray. Prenatal diagnosis 42 (1) (2021)
Yuanzhuo Chen, Linhu Liu, Dan Xia, Fenghua He, Qiyi Wang, Ting Li, Yi Lai, Shanling Liu, Zhu Zhang
Comparison of spontaneous fetal loss rates between women with singleton and twin pregnancies after mid-trimester amniocentesis - A historical cohort study. Prenatal diagnosis 40 (10) (2020)
Ting Hu, Zhu Zhang, Jiamin Wang, Qinqin Li, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system. Prenatal diagnosis 39 (12) (2019)
Hong Liao, Shanling Liu, He Wang, Hang Su, Zhenjun Liu
Enhanced antifungal activity of bovine lactoferrin-producing probiotic Lactobacillus casei in the murine model of vulvovaginal candidiasis. BMC microbiology 19 (1) (2019)
Zhu Zhang, Ting Hu, Jiamin Wang, Qinqin Li, He Wang, Shanling Liu
Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm. BioMed research international 2019 (2019)
Ting Hu, Zhu Zhang, Jiamin Wang, Qinqin Li, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu
Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation. BioMed research international 2019 (2019)