Ye Cheng

Wanyuan Road 399
Shanghai, 201102, China

Last Updated: 09/26/2026

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Found 21 publications

Identifying SHROOM4 as a novel X-linked susceptibility gene for cerebral palsy in Chinese males.

Identifying SHROOM4 as a novel X-linked susceptibility gene for cerebral palsy in Chinese males.

Journal: BMC pediatrics

Published: March 23, 2026

Liver transcriptome sequencing contributes to the molecular diagnosis of genetic liver diseases.

Liver transcriptome sequencing contributes to the molecular diagnosis of genetic liver diseases.

Journal: Hepatology (Baltimore, Md.)

Published: October 11, 2025

TRAP5 Inhibition Targeting Scar-Associated Macrophages Ameliorates Acute Kidney Injury to Chronic Kidney Disease Transition.

TRAP5 Inhibition Targeting Scar-Associated Macrophages Ameliorates Acute Kidney Injury to Chronic Kidney Disease Transition.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: October 09, 2025

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

A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasis.

A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasis.

Journal: Hepatology (Baltimore, Md.)

Published: June 05, 2025

Untargeted lipidomics profiling provides novel insights into pediatric patients with sepsis: an exploratory study.

Untargeted lipidomics profiling provides novel insights into pediatric patients with sepsis: an exploratory study.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: February 16, 2025

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

A novel prognostic signature and immune microenvironment characteristics associated with disulfidptosis in papillary thyroid carcinoma based on single-cell RNA sequencing.

A novel prognostic signature and immune microenvironment characteristics associated with disulfidptosis in papillary thyroid carcinoma based on single-cell RNA sequencing.

Journal: Frontiers in cell and developmental biology

Published: October 06, 2023

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

Gain-of-Function KIDINS220 Variants Disrupt Neuronal Development and Cause Cerebral Palsy.

Gain-of-Function KIDINS220 Variants Disrupt Neuronal Development and Cause Cerebral Palsy.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 06, 2023

Activation of GPER1 in macrophages ameliorates UUO-induced renal fibrosis.

Activation of GPER1 in macrophages ameliorates UUO-induced renal fibrosis.

Journal: Cell death & disease

Published: July 19, 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

Showing 1-12 of 21

Last Updated: 09/26/2026