Decoding GTF3A deficiency as a novel inborn error of immunity - expanding the horizons of severe combined immune deficiencies

Exploring the Immune Horizon: Systemic Inflammatory Diseases in the Era of SARS-CoV-2 and Beyond

‘Immunodeficiency-causing IKAROS mutations in the bright sunlight’, A comprehensive study characterizing the genetic and immunological heterogeneity in IKAROS-mediated immune diseases.

From bed to bench: Insights from novel pathogenic RC3H1 and ZC3H12A variants in patients with autoimmune disease and immune dysregulation syndromes.

Harnessing transcriptome and proteome wide analyses and engineered reporter assays to unravel the immunopathogenesis of 'multisystem inflammatory syndrome in children' (MIS-C).

Role of hypoxia in dendritic cell biology and pathogenesis of asthma

The role of the C3H1 zinc finger protein Roquin1 in inflammation, from a genetic survey in hyperinflammatory disorders to therapeutic applicability.

CONDITIONAL: COvid-19: iNterplay between genetic preDisposITION and immunologicAl Landscape