Associated Papers
Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency.
Abolhassani H et al.
Journal of Human Immunity, 2025
Genomic crossroads between non-Hodgkin's lymphoma and common variable immunodeficiency.
Guevara-Hoyer K et al.
Frontiers in Immunology, 2022
35990641 (PubMed )
Supplement: DataSheet_2.xlsx › Supp_Table_1
Monogenic mutations associated with IgA deficiency.
Abolhassani H et al.
Expert Review of Clinical Immunology, 2016
Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
van Schouwenburg PA et al.
Clinical Immunology (orlando, Fla.), 2015
26122175 (PubMed )
Supplement: NIHMS64345-supplement-Supplementary_tables.xlsx › Table_S1
Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.
Freiberger T et al.
Human Immunology, 2012
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Salzer U et al.
Blood, 2009
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.
Pan-Hammarström Q et al.
Nature Genetics, 2007
Select a paper to view details