Miaomiao Li

No. 308 Ningxia Road
Qingdao, 266071, China

Last Updated: 09/26/2026

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Found 26 publications

Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome.

Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome.

Journal: Seizure

Published: February 23, 2026

Microbiome and metabolite signatures for cirrhosis to HCC risk stratification: progress, controversies, and gaps.

Microbiome and metabolite signatures for cirrhosis to HCC risk stratification: progress, controversies, and gaps.

Journal: Frontiers in cellular and infection microbiology

Published: January 21, 2026

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation.

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation.

Journal: Frontiers in genetics

Published: October 09, 2025

Laboratory Test Indirectly Reveals the Unreliability of RNA-Dependent 16S rRNA Amplicon Sequences in Detecting the Gut Bacterial Diversity of Delia antiqua.

Laboratory Test Indirectly Reveals the Unreliability of RNA-Dependent 16S rRNA Amplicon Sequences in Detecting the Gut Bacterial Diversity of Delia antiqua.

Journal: Insects

Published: May 13, 2025

A novel high-entropy TiVCrMoC3Tx assisted LDI MS for serum metabolic fingerprint in rheumatoid arthritis.

A novel high-entropy TiVCrMoC3Tx assisted LDI MS for serum metabolic fingerprint in rheumatoid arthritis.

Journal: Journal of pharmaceutical analysis

Published: February 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

Common and Rare DUOX Variants in Patients With Congenital Hypothyroidism: Case-control Study and Family-based Analysis.

Common and Rare DUOX Variants in Patients With Congenital Hypothyroidism: Case-control Study and Family-based Analysis.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 08, 2025

Potentially diagnostic and prognostic roles of piRNAs/PIWIs in pancreatic cancer: A review.

Potentially diagnostic and prognostic roles of piRNAs/PIWIs in pancreatic cancer: A review.

Journal: Biochimica et biophysica acta. Reviews on cancer

Published: December 13, 2024

Characteristics of glucose-6-phosphate dehydrogenase mutations in newborns with deficiency from 2021 to 2022 in the Heze area of China.

Characteristics of glucose-6-phosphate dehydrogenase mutations in newborns with deficiency from 2021 to 2022 in the Heze area of China.

Journal: Frontiers in immunology

Published: July 31, 2024

Relationship between TYG mediated pregnancy diabetes history and SII in American women: a retrospective cohort study of NHANES 2011-2018.

Relationship between TYG mediated pregnancy diabetes history and SII in American women: a retrospective cohort study of NHANES 2011-2018.

Journal: BMC endocrine disorders

Published: July 27, 2024

Genetic and functional analysis of TUBB1 variants in congenital hypothyroidism.

Genetic and functional analysis of TUBB1 variants in congenital hypothyroidism.

Journal: Endokrynologia Polska

Published: July 03, 2024

Rearing Axenic Delia antiqua with Half-Fermented Sterile Diets.

Rearing Axenic Delia antiqua with Half-Fermented Sterile Diets.

Journal: Journal of visualized experiments : JoVE

Published: January 08, 2024

Showing 1-12 of 26

Last Updated: 09/26/2026