Sort   by:  
 Page size 
UnknownFANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Not available
S-EPMC4550823 | biostudies-literature
UnknownEtiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation.
Not available
S-EPMC6041155 | biostudies-literature
UnknownAlternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report.
Not available
S-EPMC6591742 | biostudies-literature
UnknownLarge-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer.
Not available
S-EPMC12657754 | biostudies-literature
UnknownNo evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
Not available
S-EPMC4938802 | biostudies-literature
UnknownSNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival.
Not available
S-EPMC4741978 | biostudies-literature
UnknownCommon variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC2893806 | biostudies-literature
UnknownAssociation of ESR1 gene tagging SNPs with breast cancer risk.
Not available
S-EPMC2722230 | biostudies-literature
UnknownAssociation of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Not available
S-EPMC5340257 | biostudies-literature
UnknownLow penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.
Not available
S-EPMC3140824 | biostudies-literature
Sort   by:  
 Page size