Isabelle Meyts

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 230 publications

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

Entering the era of somatic variant sequencing in immune dysregulation: comment on the article by Fu et al.

Entering the era of somatic variant sequencing in immune dysregulation: comment on the article by Fu et al.

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

Published: April 03, 2026

Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling, 2026: International consensus statement on behalf of the European Society for Immunodeficiencies/European Society for Blood and Marrow Transplantation-Inborn Errors Working Party and ERN-RITA.

Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling, 2026: International consensus statement on behalf of the European Society for Immunodeficiencies/European Society for Blood and Marrow Transplantation-Inborn Errors Working Party and ERN-RITA.

Journal: The Journal of allergy and clinical immunology

Published: March 09, 2026

Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling (2026). An international consensus statement on behalf of the ESID/EBMT-IEWP and ERN-RITA.

Guidance on JAK inhibitor treatment for inborn errors of JAK-STAT signaling (2026). An international consensus statement on behalf of the ESID/EBMT-IEWP and ERN-RITA.

Journal: The Journal of allergy and clinical immunology

Published: March 09, 2026

Two novel kindreds with autosomal recessive STAT2 deficiency.

Two novel kindreds with autosomal recessive STAT2 deficiency.

Journal: Journal of human immunity

Published: March 04, 2026

Adenosine deaminase type 2 deficiency: From rare to common.

Adenosine deaminase type 2 deficiency: From rare to common.

Journal: Journal of human immunity

Published: January 27, 2026

Correction to: An international survey of allogeneic hematopoietic cell transplantation for X-linked agammaglobulinemia.

Correction to: An international survey of allogeneic hematopoietic cell transplantation for X-linked agammaglobulinemia.

Journal: Journal of clinical immunology

Published: January 21, 2026

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Journal: Clinical immunology (Orlando, Fla.)

Published: January 16, 2026

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: The Journal of experimental medicine

Published: January 09, 2026

Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function.

Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function.

Journal: The Journal of clinical investigation

Published: January 02, 2026

The seven enigmas of SARS-CoV-2: from the past to the future.

The seven enigmas of SARS-CoV-2: from the past to the future.

Journal: Journal of human immunity

Published: December 05, 2025

Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylation.

Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylation.

Journal: Molecular genetics and metabolism

Published: November 10, 2025

Showing 1-12 of 230

Last Updated: 09/26/2026