Associated Papers
Germline Variants in the Immune Response-Related Genes: Possible Modifying Effect on Age-Dependent BRCA1 Penetrance in Breast Cancer Patient.
Kuligina ES et al.
Cancers, 2025
41374957 (PubMed )
Supplement: cancers-17-03756-s001.zip › Table_S4a.xlsx › Table_S4a
Common origin and somatic mutation patterns of composite lymphomas and leukemias.
Berg V et al.
Leukemia, 2025
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J et al.
The Journal of Experimental Medicine, 2021
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).
Bisgin A et al.
Scientific Reports, 2021
33859323 (PubMed )
Supplement: 41598_2021_87898_MOESM2_ESM.pdf
Somatic mutations in the DNA repairome in prostate cancers in African Americans and Caucasians.
Yadav S et al.
Oncogene, 2020
32300177 (PubMed )
Supplement: 41388_2020_1280_MOESM3_ESM.xlsx › Main_Sheet_
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
27490946 (PubMed )
Supplement: pone.0159609.s002.xlsx › Results_Discovery_phase_I
IκBKβ and NFκB1, NSAID use and risk of colorectal cancer in the Colon Cancer Family Registry.
Seufert BL et al.
Carcinogenesis, 2013
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors.
Wong ML et al.
Molecular Psychiatry, 2012
Functional nonsynonymous single nucleotide polymorphisms from the TGF-beta protein interaction network.
Savas S et al.
Physiological Genomics, 2007
Genetic variation and the mitogen-activated protein kinase (MAPK) signaling pathway.
Cho S et al.
Omics : a Journal of Integrative Biology, 2006
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