Yinglei Xu
16 Jiangsu Road
Qingdao, 266003, China
Qingdao, 266003, China
Last Updated: 09/26/2026
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Found 16 publications
Association of NLRP3 and IL-4 VNTR polymorphisms and genetic susceptibility to preeclampsia: A case-control study.
Journal: Pregnancy hypertension
Published: December 29, 2023
Impact of SLC23A1 and SLC23A2 Polymorphisms on the Risk for Preeclampsia in a Chinese Han Population.
Journal: Journal of nutritional science and vitaminology
Published: October 30, 2022
Analysis of genetic variant in a patient with juvenile meterochromic leukodystrophy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 02, 2022
The role of VCAM-1 in diabetic retinopathy: A systematic review and meta-analysis.
Journal: Journal of diabetes and its complications
Published: August 03, 2022
A review of key cytokines based on gene polymorphism in the pathogenesis of pre-eclampsia.
Journal: American journal of reproductive immunology (New York, N.Y. : 1989)
Published: August 10, 2021
The Value of Circulating microRNAs for Diagnosis and Prediction of Preeclampsia: a Meta-analysis and Systematic Review.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: April 27, 2021
Polymorphisms of TGF-β1 and TGF-β3 in Chinese women with gestational diabetes mellitus.
Journal: BMC pregnancy and childbirth
Published: August 18, 2020
Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese family.
Journal: The journal of gene medicine
Published: January 16, 2020
Protective roles and mechanisms of rosmarinic acid in cyclophosphamide-induced premature ovarian failure.
Journal: Journal of biochemical and molecular toxicology
Published: October 29, 2019
Hypomethylation of DNA promoter upregulates ADAMTS7 and contributes to HTR-8/SVneo and JEG-3 cells abnormalities in pre-eclampsia.
Journal: Placenta
Published: October 28, 2019
Targeted regions sequencing identified four novel PNPLA1 mutations in two Chinese families with autosomal recessive congenital ichthyosis.
Journal: Molecular genetics & genomic medicine
Published: September 13, 2019
A Novel CD40L Mutation Associated with X-Linked Hyper IgM Syndrome in a Chinese Family.
Journal: Immunological investigations
Published: August 13, 2019
Last Updated: 09/26/2026