Yanshan Liu

Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, 100005, China

Last Updated: 09/26/2026

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Found 12 publications

Genotype mutations and phenotypes of 30 cases with epilepsy related to fever sensitivity in children.

Genotype mutations and phenotypes of 30 cases with epilepsy related to fever sensitivity in children.

Journal: Frontiers in neurology
Published: December 13, 2025

Dynamics of the respiratory infectome in children with community-acquired pneumonia: insights from large and short time-scale analyses.

Dynamics of the respiratory infectome in children with community-acquired pneumonia: insights from large and short time-scale analyses.

Journal: Microbiology spectrum
Published: October 27, 2025

A Novel GUCY2D Frameshift Deletion Identified in a Patient with Leber Congenital Amaurosis 1: A Case Report.

A Novel GUCY2D Frameshift Deletion Identified in a Patient with Leber Congenital Amaurosis 1: A Case Report.

Journal: Case reports in ophthalmology
Published: July 31, 2025

Retinal editome profiling in mice reveals RNA editing in key developmental genes associated with retinitis pigmentosa.

Retinal editome profiling in mice reveals RNA editing in key developmental genes associated with retinitis pigmentosa.

Journal: PeerJ
Published: March 27, 2025

Association of alterations in transcriptomics and intestinal immune responses with Bifidobacterium longum BAA2573 in improving dextran sulfate sodium-induced colitis.

Association of alterations in transcriptomics and intestinal immune responses with Bifidobacterium longum BAA2573 in improving dextran sulfate sodium-induced colitis.

Journal: BMC gastroenterology
Published: March 11, 2025

Bulk and single-cell RNA-seq analyses reveal canonical RNA editing associated with microglia homeostasis and its role in sepsis-associated encephalopathy.

Bulk and single-cell RNA-seq analyses reveal canonical RNA editing associated with microglia homeostasis and its role in sepsis-associated encephalopathy.

Journal: Neuroscience
Published: May 28, 2024

Clinical characteristics analysis of 24 cases of pediatric MOG antibody-associated diseases.

Clinical characteristics analysis of 24 cases of pediatric MOG antibody-associated diseases.

Journal: Multiple sclerosis and related disorders
Published: February 24, 2024

A Chromosomal-Level Genome of Dermatophagoides farinae, a Common Allergenic Mite Species.

A Chromosomal-Level Genome of Dermatophagoides farinae, a Common Allergenic Mite Species.

Journal: International journal of genomics
Published: October 28, 2023

A female patient carrying a novel DMD mutation with non-random X-chromosome inactivation from a DMD family.

A female patient carrying a novel DMD mutation with non-random X-chromosome inactivation from a DMD family.

Journal: BMC medical genomics
Published: October 23, 2023

Functional analysis of a novel de novo SCN2A variant in a patient with seizures refractory to oxcarbazepine.

Functional analysis of a novel de novo SCN2A variant in a patient with seizures refractory to oxcarbazepine.

Journal: Frontiers in molecular neuroscience
Published: February 06, 2023

Germline intergenic duplications at Xq26.1 underlie Bazex-Dupré-Christol basal cell carcinoma susceptibility syndrome.

Germline intergenic duplications at Xq26.1 underlie Bazex-Dupré-Christol basal cell carcinoma susceptibility syndrome.

Journal: The British journal of dermatology
Published: March 01, 2022

Pathogenic mutations in two Chinese patients exhibiting severe early-onset obesity.

Pathogenic mutations in two Chinese patients exhibiting severe early-onset obesity.

Journal: Science China. Life sciences
Published: December 10, 2018
Showing 1-12 of 12

Last Updated: 09/26/2026