Yucui Zang
Qingdao, China
Last Updated: 09/26/2026
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Found 10 publications
Autism Spectrum Disorder Caused by a Novel De Novo SCN2A Mutation: A Case Report.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: February 01, 2026
Association of NLRP3 and IL-4 VNTR polymorphisms and genetic susceptibility to preeclampsia: A case-control study.
Journal: Pregnancy hypertension
Published: December 29, 2023
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
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study.
Journal: BMC pregnancy and childbirth
Published: June 11, 2021
DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-in-situ With Congenital Hypothyroidism.
Journal: Frontiers in endocrinology
Published: November 13, 2019
Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation.
Journal: Frontiers in endocrinology
Published: February 22, 2019
Mutations in ASH1L confer susceptibility to Tourette syndrome.
Journal: Molecular psychiatry
Published: February 21, 2019
Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis.
Journal: Journal of cellular biochemistry
Published: January 26, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026