Sven Kracker

6PUBLICATIONS
67CO-AUTHORS
Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)AutoimmunityImmunogenetics (incl. genetic immunology)Pharmacogenomics
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Publications (6)

|May 08, 2026
Ribosomal RNA processing impairments in a B cell immunodeficient patient with WDR75 variants.

|Jan 30, 2026
A heterozygous USB1 variant linked to immunodeficiency.

Alice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou

|Aug 30, 2024
RAC2 gain-of-function variants causing inborn error of immunity drive NLRP3 inflammasome activation.

Anne Doye, Paul Chaintreuil, Chantal Lagresle-Peyrou

|Jul 31, 2023
A Case Report of Folliculin-Interacting Protein 1 Deficiency.

Nidia Moreno-Corona, Alice Valagussa, Romane Thouenon

|Mar 14, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.

Romane Thouenon, Loïc Chentout, Nidia Moreno-Corona

|Oct 29, 2020
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies.

Nieves Diaz, Maria Juarez, Caterina Cancrini

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Frequent Collaborators

3 joint publications

Chantal Lagresle-Peyrou

3 joint publications

Alain Fischer

3 joint publications

Nidia Moreno-Corona

3 joint publications

Marina Cavazzana