Yuqi Yang
Zhenjiang, 212013, China
Last Updated: 09/26/2026
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Found 11 publications
SIGLEC6 impairs trophoblast function and orchestrates macrophage M1 polarization via suppression of Akt signaling in early-onset preeclampsia.
Journal: Placenta
Published: January 15, 2026
Permanent vs Transient Congenital Hypothyroidism in Chinese Children: Physical Growth and Predictive Nomogram.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 14, 2023
Trophoblast Cell Subtypes and Dysfunction in the Placenta of Individuals with Preeclampsia Revealed by Single‑Cell RNA Sequencing.
Journal: Molecules and cells
Published: August 10, 2021
Variant of TSHR is Not a Frequent Cause of Congenital Hypothyroidism in Chinese Han Patients.
Journal: International journal of general medicine
Published: May 31, 2021
Alterations in the metabolic status of amino acids in newborns of pre-eclampsia women.
Journal: Pregnancy hypertension
Published: September 25, 2020
Newborn screening for congenital hypothyroidism: A 13-year observational study
Journal: Anales de pediatria
Published: March 13, 2019
Two Infants With Beta-Ketothiolase Deficiency Identified by Newborn Screening in China.
Journal: Frontiers in genetics
Published: January 23, 2019
3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary?
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: December 06, 2018
Application of Next-Generation Sequencing Following Tandem Mass Spectrometry to Expand Newborn Screening for Inborn Errors of Metabolism: A Multicenter Study.
Journal: Frontiers in genetics
Published: October 03, 2018
Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.
Journal: Frontiers in genetics
Published: July 07, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026