Xiaomin A. Yu

Hangzhou, China

Last Updated: 09/26/2026

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Found 70 publications

Genetically defined systemic autoinflammatory diseases in pediatric patients with Behçet's disease.

Genetically defined systemic autoinflammatory diseases in pediatric patients with Behçet's disease.

Journal: Frontiers in immunology
Published: June 01, 2026

Reply.

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Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: May 02, 2026

TLR1 deficiency associates with immune dysregulation and colitis.

TLR1 deficiency associates with immune dysregulation and colitis.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 28, 2026

Endosomal signaling disorders: a new category for immune dysregulation.

Endosomal signaling disorders: a new category for immune dysregulation.

Journal: Trends in molecular medicine
Published: January 30, 2026

A Multicenter Integrative Cohort Characterizing the Genetic, Clinical, and Transcriptomic Features of ACP5 Deficiency.

A Multicenter Integrative Cohort Characterizing the Genetic, Clinical, and Transcriptomic Features of ACP5 Deficiency.

Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: January 25, 2026

Drop-Shaped Optical Microfiber Enabled Biomechanical Sensor.

Drop-Shaped Optical Microfiber Enabled Biomechanical Sensor.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: January 16, 2026

Author Correction: Loss-of-function mutations in PLD4 lead to systemic lupus erythematosus.

Author Correction: Loss-of-function mutations in PLD4 lead to systemic lupus erythematosus.

Journal: Nature
Published: October 10, 2025

Landscape of Somatic Mutations in a Large Cohort of Chinese Patients With Immune Dysregulations.

Landscape of Somatic Mutations in a Large Cohort of Chinese Patients With Immune Dysregulations.

Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: September 18, 2025

IRAK2 deficiency causes immune dysregulation through defective Myddosome assembly and enhanced interferon responses.

IRAK2 deficiency causes immune dysregulation through defective Myddosome assembly and enhanced interferon responses.

Journal: Nature communications
Published: September 05, 2025

OGFRL1 Deficiency Causes Chronic Recurrent Multifocal Osteomyelitis Via Pathologic Osteoclastogenesis, With Therapeutic Response to Tumor Necrosis Factor Inhibitor.

OGFRL1 Deficiency Causes Chronic Recurrent Multifocal Osteomyelitis Via Pathologic Osteoclastogenesis, With Therapeutic Response to Tumor Necrosis Factor Inhibitor.

Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: July 05, 2025

Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution.

Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution.

Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025

Multicenter international cohort study of haploinsufficiency of A20 reveals novel genetic architecture and phenotypic evolution.

Multicenter international cohort study of haploinsufficiency of A20 reveals novel genetic architecture and phenotypic evolution.

Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025
Showing 1-12 of 70

Last Updated: 09/26/2026