Xinzhuang Yang

Peking Union Medical College Hospital, Chinese Academy Of Medical Sciences & Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 15 publications

HLA genotyping and clinical characteristics of early-onset and late-onset anti-LGI1 encephalitis: a single-center cohort study in China.

HLA genotyping and clinical characteristics of early-onset and late-onset anti-LGI1 encephalitis: a single-center cohort study in China.

Journal: Frontiers in immunology

Published: December 02, 2025

HLA Class I Haplotype in Glutamic Acid Decarboxylase Antibody-Associated Neurological Disease.

HLA Class I Haplotype in Glutamic Acid Decarboxylase Antibody-Associated Neurological Disease.

Journal: European journal of neurology

Published: July 21, 2025

Applying Genetic Risk Score to Improve Risk Assessment of New-Onset Lupus Nephritis in Systemic Lupus Erythematosus: A Large-Scale Prospective Cohort Study.

Applying Genetic Risk Score to Improve Risk Assessment of New-Onset Lupus Nephritis in Systemic Lupus Erythematosus: A Large-Scale Prospective Cohort Study.

Journal: MedComm

Published: June 09, 2025

Association of Rare Variants in Pulmonary Arterial Hypertension-Related Genes With a Distinct Vasculopathy Phenotype and Worse Outcomes in Patients With Systemic Lupus Erythematosus-Associated Pulmonary Arterial Hypertension.

Association of Rare Variants in Pulmonary Arterial Hypertension-Related Genes With a Distinct Vasculopathy Phenotype and Worse Outcomes in Patients With Systemic Lupus Erythematosus-Associated Pulmonary Arterial Hypertension.

Journal: Chest

Published: April 22, 2025

Rare TRAF5 coding variants in systemic lupus erythematosus patients aggravate pulmonary hypertension via endothelial dysfunction.

Rare TRAF5 coding variants in systemic lupus erythematosus patients aggravate pulmonary hypertension via endothelial dysfunction.

Journal: Innovation (Cambridge (Mass.))

Published: January 28, 2025

RNF213 in moyamoya disease: Genotype-phenotype association and the underlying mechanism.

RNF213 in moyamoya disease: Genotype-phenotype association and the underlying mechanism.

Journal: Chinese medical journal

Published: June 14, 2023

A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy.

A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy.

Journal: BMC medical genomics

Published: January 30, 2023

Association Study Identified HLA-DQA1 as a Novel Genetic Risk of Systemic Lupus Erythematosus-Associated Pulmonary Arterial Hypertension.

Association Study Identified HLA-DQA1 as a Novel Genetic Risk of Systemic Lupus Erythematosus-Associated Pulmonary Arterial Hypertension.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: January 09, 2023

Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.

Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.

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

Published: October 04, 2020

Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis.

Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis.

Journal: Frontiers in bioengineering and biotechnology

Published: August 19, 2019

Identification of novel FBN1 variations implicated in congenital scoliosis.

Identification of novel FBN1 variations implicated in congenital scoliosis.

Journal: Journal of human genetics

Published: July 30, 2019

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.

Journal: Human mutation

Published: March 04, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026