Yoann Seeleuthner

7PUBLICATIONS

282CO-AUTHORS

Gene and molecular therapyMedical infection agents (incl. prions)Infant and child healthImmunogenetics (incl. genetic immunology)Medical virology

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Publications (7)

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|May 29, 2026

STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy.

|Nov 22, 2024

Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C).

Evangelos Bellos, Dilys Santillo, Pierre Vantourout

|Apr 18, 2024

Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.

Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila

|Nov 03, 2022

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.

Masato Ogishi, Rui Yang, Rémy Rodriguez

|Sep 12, 2022

Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency.

Masato Ogishi, Andrés Augusto Arias, Rui Yang

|Apr 20, 2022

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes.

Paul Bastard, Kuang-Chih Hsiao, Qian Zhang

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Frequent Collaborators

7 joint publications

Jean-Laurent Casanova

Emmanuelle Jouanguy

Laurent Abel

Jacinta Bustamante

Stephanie Boisson-Dupuis

Shen-Ying Zhang

Peng Zhang

Vivien Béziat

Maya Chrabieh

Qian Zhang

Frequent Collaborators

7 joint publications

Jean-Laurent Casanova

5 joint publications

Emmanuelle Jouanguy

5 joint publications

Laurent Abel

4 joint publications

Jacinta Bustamante