Associated Papers
The evolutionary impact of childhood cancer on the human gene pool.
Stoltze UK et al.
Nature Communications, 2024
38424437 (PubMed )
Supplement: 41467_2024_45975_MOESM4_ESM.xlsx › Supplementary_Data_11
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes.
Byrjalsen A et al.
Plos Genetics, 2020
33332384 (PubMed )
Supplement: pgen.1009231.s001.xlsx › VUS
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
de Valles-Ibáñez G et al.
Frontiers in Immunology, 2018
29867916 (PubMed )
Supplement: data_sheet_1.PDF
Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.
Sathkumara HD et al.
International Journal of Immunogenetics, 2015
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
Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.
Janzi M et al.
Genes and Immunity, 2012
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.
Mohammadi J et al.
Journal of Clinical Immunology, 2009
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