Associated Papers
Reply to Bousdar et al.: Common inherited loss-of-function mutations in the innate sensor NOD2 contribute to exceptional immune response to cancer immunotherapy.
Barnet MB et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
Contrasting outcomes of inherited NOD2 loss-of-function variants on immunotherapy response in cancer.
Bousdar N et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.
Horowitz JE et al.
Scientific Reports, 2021
33692434 (PubMed )
Supplement: 41598_2021_84938_MOESM2_ESM.xlsx › Table_S4
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.
Vidmar L et al.
Scientific Reports, 2019
31235738 (PubMed )
Supplement: 41598_2019_45598_MOESM2_ESM.xlsx › Sheet1
Single nucleotide polymorphisms in pathogen recognition receptor genes are associated with susceptibility to meningococcal meningitis in a pediatric cohort.
van Well GT et al.
Plos One, 2013
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