Tom Le Voyer

Paris, 75015, France

Last Updated: 09/26/2026

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Found 62 publications

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 31, 2026

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

Journal: medRxiv : the preprint server for health sciences

Published: April 10, 2026

Intronic branchpoint-to-acceptor variants underlying inborn errors of immunity.

Intronic branchpoint-to-acceptor variants underlying inborn errors of immunity.

Journal: Journal of human immunity

Published: December 15, 2025

A WAS promoter variant underlying Wiskott-Aldrich syndrome in two kindreds.

A WAS promoter variant underlying Wiskott-Aldrich syndrome in two kindreds.

Journal: Journal of human immunity

Published: December 03, 2025

BIRC3 (Encoding Cellular Inhibitor of Apoptosis Protein 2) Variants Result in Dysregulated Receptor-Interacting Protein Kinase 1 Signaling Leading to Increased Epithelial Cell Death and Are Associated With Monogenic Crohn's Disease.

BIRC3 (Encoding Cellular Inhibitor of Apoptosis Protein 2) Variants Result in Dysregulated Receptor-Interacting Protein Kinase 1 Signaling Leading to Increased Epithelial Cell Death and Are Associated With Monogenic Crohn's Disease.

Journal: Gastroenterology

Published: October 24, 2025

Two different forms of inherited human TCRα chain deficiency.

Two different forms of inherited human TCRα chain deficiency.

Journal: Journal of human immunity

Published: October 17, 2025

Good? A very long COVID-19.

Good? A very long COVID-19.

Journal: Journal of human immunity

Published: August 22, 2025

Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2).

Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2).

Journal: The Journal of experimental medicine

Published: July 01, 2025

Human inborn errors of the alternative NF-κB pathway.

Human inborn errors of the alternative NF-κB pathway.

Journal: Journal of human immunity

Published: May 20, 2025

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

Journal: Nature immunology

Published: December 16, 2024

Affinity-matured B cell responses neutralizing type-I interferons underlie severe viral infections.

Affinity-matured B cell responses neutralizing type-I interferons underlie severe viral infections.

Journal: Cell

Published: October 31, 2024

A sensitive assay for measuring whole-blood responses to type I IFNs.

A sensitive assay for measuring whole-blood responses to type I IFNs.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 23, 2024

Showing 1-12 of 62

Last Updated: 09/26/2026