Yimeng D. Qiao

Wanyuan Road 399
Shanghai, 201102, China

Last Updated: 09/26/2026

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Found 14 publications

Nodular fasciitis in children: a clinicopathological analysis of twenty-four cases

Nodular fasciitis in children: a clinicopathological analysis of twenty-four cases

Journal: Zhonghua bing li xue za zhi = Chinese journal of pathology

Published: January 06, 2026

X-chromosomal genetic variants and haplotype analysis in male cerebral palsy patients: insights into genetic susceptibility and sex-specific risk.

X-chromosomal genetic variants and haplotype analysis in male cerebral palsy patients: insights into genetic susceptibility and sex-specific risk.

Journal: Journal of neurodevelopmental disorders

Published: June 20, 2025

Degradation of myosmine by a novel bacterial strain Sphingopyxis sp. J-6 and its degradation pathways.

Degradation of myosmine by a novel bacterial strain Sphingopyxis sp. J-6 and its degradation pathways.

Journal: Journal of hazardous materials

Published: October 21, 2024

Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study.

Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study.

Journal: Genes & diseases

Published: January 30, 2024

Genetic variants in the HLA region contribute to the risk of cerebral palsy.

Genetic variants in the HLA region contribute to the risk of cerebral palsy.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: September 26, 2023

Targeting the metabolic profile of amino acids to identify the key metabolic characteristics in cerebral palsy.

Targeting the metabolic profile of amino acids to identify the key metabolic characteristics in cerebral palsy.

Journal: Frontiers in molecular neuroscience

Published: June 19, 2023

Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.

Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.

Journal: Nature medicine

Published: June 15, 2023

Clinical variables and genetic variants associated with perioperative anaphylaxis in Chinese Han population: A pilot study.

Clinical variables and genetic variants associated with perioperative anaphylaxis in Chinese Han population: A pilot study.

Journal: The World Allergy Organization journal

Published: June 06, 2023

An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population.

An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population.

Journal: BMC medical genomics

Published: May 15, 2022

Case Report: Novel MFSD8 Variants in a Chinese Family With Neuronal Ceroid Lipofuscinoses 7.

Case Report: Novel MFSD8 Variants in a Chinese Family With Neuronal Ceroid Lipofuscinoses 7.

Journal: Frontiers in genetics

Published: November 02, 2021

TEP1 is a risk gene for sporadic cerebral palsy.

TEP1 is a risk gene for sporadic cerebral palsy.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: May 14, 2021

The Association Study of IL-23R Polymorphisms With Cerebral Palsy in Chinese Population.

The Association Study of IL-23R Polymorphisms With Cerebral Palsy in Chinese Population.

Journal: Frontiers in neuroscience

Published: July 31, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026