Mengmeng Han

Qingdao, China

Last Updated: 09/26/2026

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Found 12 publications

MIR210HG promotes preeclampsia progression through CDHR5.

MIR210HG promotes preeclampsia progression through CDHR5.

Journal: Hypertension in pregnancy

Published: August 17, 2026

Cell-free RNAs in maternal peripheral blood as potential biomarkers of preeclampsia: a review.

Cell-free RNAs in maternal peripheral blood as potential biomarkers of preeclampsia: a review.

Journal: Reproductive biology and endocrinology : RB&E

Published: June 25, 2025

Effect of PVP and HPMC on production of indomethacin amorphous nanoparticles: experiments and molecular dynamics simulations.

Effect of PVP and HPMC on production of indomethacin amorphous nanoparticles: experiments and molecular dynamics simulations.

Journal: Drug development and industrial pharmacy

Published: April 20, 2025

The genotype-phenotype association of retinitis pigmentosa in a Chinese population: Analysis of three new cases and literature review.

The genotype-phenotype association of retinitis pigmentosa in a Chinese population: Analysis of three new cases and literature review.

Journal: Molecular vision

Published: January 27, 2025

Genetic analysis of a child with Multiple congenital anomalies-hypotonia-seizures syndrome 1 due to variant of PIGN gene

Genetic analysis of a child with Multiple congenital anomalies-hypotonia-seizures syndrome 1 due to variant of PIGN gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 29, 2024

TSFFM: Depression detection based on latent association of facial and body expressions.

TSFFM: Depression detection based on latent association of facial and body expressions.

Journal: Computers in biology and medicine

Published: July 10, 2023

Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism.

Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism.

Journal: Endocrine

Published: April 27, 2022

The first Chinese case of Vici syndrome with novel compound heterozygous sequence variants in EPG5.

The first Chinese case of Vici syndrome with novel compound heterozygous sequence variants in EPG5.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: June 06, 2021

Polymorphisms of TGF-β1 and TGF-β3 in Chinese women with gestational diabetes mellitus.

Polymorphisms of TGF-β1 and TGF-β3 in Chinese women with gestational diabetes mellitus.

Journal: BMC pregnancy and childbirth

Published: August 18, 2020

A Novel CD40L Mutation Associated with X-Linked Hyper IgM Syndrome in a Chinese Family.

A Novel CD40L Mutation Associated with X-Linked Hyper IgM Syndrome in a Chinese Family.

Journal: Immunological investigations

Published: August 13, 2019

A novel ATRX mutation causes Smith‑Fineman‑Myers syndrome in a Chinese family.

A novel ATRX mutation causes Smith‑Fineman‑Myers syndrome in a Chinese family.

Journal: Molecular medicine reports

Published: June 09, 2019

Mutations in ASH1L confer susceptibility to Tourette syndrome.

Mutations in ASH1L confer susceptibility to Tourette syndrome.

Journal: Molecular psychiatry

Published: February 21, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026