Stuart G. Tangye

St Vincent's Clinical School
Sydney, NSW 2052, Australia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 202 publications

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: medRxiv : the preprint server for health sciences

Published: August 01, 2026

Interfering with innate immunity: type I IFNs and avian influenza susceptibility.

Interfering with innate immunity: type I IFNs and avian influenza susceptibility.

Journal: EBioMedicine

Published: July 17, 2026

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Journal: bioRxiv : the preprint server for biology

Published: April 03, 2026

Human CD21loT-bet+ B cells: Not as easy as "ABC"!

Human CD21loT-bet+ B cells: Not as easy as "ABC"!

Journal: Journal of human immunity

Published: February 09, 2026

Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: Single-center cohort analysis.

Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: Single-center cohort analysis.

Journal: The Journal of allergy and clinical immunology

Published: January 25, 2026

The spectrum of tonsillar involvement in chronic lymphocytic leukemia (CLL).

The spectrum of tonsillar involvement in chronic lymphocytic leukemia (CLL).

Journal: Leukemia & lymphoma

Published: January 20, 2026

Deleterious germline CARD11 gain-of-function variants alter human B-cell and CD4+ T-cell differentiation and function.

Deleterious germline CARD11 gain-of-function variants alter human B-cell and CD4+ T-cell differentiation and function.

Journal: Clinical and experimental immunology

Published: December 24, 2025

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Journal: The Journal of experimental medicine

Published: October 27, 2025

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: The Journal of experimental medicine

Published: October 01, 2025

A novel heterozygous pathogenic AIRE variant causing autoimmunity but not infectious susceptibility.

A novel heterozygous pathogenic AIRE variant causing autoimmunity but not infectious susceptibility.

Journal: Journal of human immunity

Published: July 11, 2025

NK cell dysfunction and interferon-γ production underlie autoinflammation in mevalonate kinase deficiency.

NK cell dysfunction and interferon-γ production underlie autoinflammation in mevalonate kinase deficiency.

Journal: Immunity

Published: June 26, 2025

Human LY9 governs CD4+ T cell IFN-γ immunity to Mycobacterium tuberculosis.

Human LY9 governs CD4+ T cell IFN-γ immunity to Mycobacterium tuberculosis.

Journal: Science immunology

Published: May 30, 2025

Showing 1-12 of 202

Last Updated: 09/26/2026