Suranjith L. Seneviratne

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

Desirée Schubert, Claudia Bode, Rupert Kenefeck et al. · Nature Medicine · 2014 · 805 citations · Full text

Immunogenetics, Autoimmune Disease, Immunodeficiencies +12

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood et al. · The American Journal of Human Genetics · 2016 · 463 citations · Full text

Whole-genome Sequencing, Allelic Variant, Genetic Disorder +11

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects

Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich et al. · Journal of Allergy and Clinical Immunology · 2018 · 423 citations · Full text

Clinical Immunology, Allergy, Lymphocyte Development +12

Longitudinal Analysis of CD8⁺T Cells Specific for Structural and Nonstructural Hepatitis B Virus Proteins in Patients with Chronic Hepatitis B: Implications for Immunotherapy

George Webster, Stephanie Reignat, David J. Brown et al. · Journal of Virology · 2004 · 383 citations · Full text

The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency

Laura Gámez‐Díaz, Dietrich August, Polina Stepensky et al. · Journal of Allergy and Clinical Immunology · 2016 · 285 citations · Full text

Protein Function, Protein Expression, Genetic Disorder +10