Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

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http://www.wikidata.org/entity/Q28652308

Q28652308

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Multigene testing of moderate-risk genes: be mindful of the missense Ciliogenesis and the DNA damage response: a stressful relationship DNA repair genes implicated in triple negative familial non-BRCA1/2 breast cancer predisposition.ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry.Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.Gene-panel sequencing and the prediction of breast-cancer risk.Identification, genetic testing, and management of hereditary melanoma.Association of the nibrin gene (NBN) variants with breast cancer.No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.DNA Methylation Heterogeneity Patterns in Breast Cancer Cell Lines Genomic Disparities in Breast Cancer Among Latinas.Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment.Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway.Blind prediction of deleterious amino acid variations with SNPs&GO.Personalised Medicine: Genome Maintenance Lessons Learned from Studies in Yeast as a Model Organism.Missense variant pathogenicity predictors generalize well across a range of function-specific prediction challenges.Hereditary breast and ovarian cancer: new genes in confined pathways.Outcomes of retesting BRCA negative patients using multigene panels.Inherited Cancer in the Age of Next-Generation Sequencing.Next-Generation Sequencing Reveals a Nonsense Mutation (p.Arg364Ter) in MRE11A Gene in an Indian Patient with Familial Breast Cancer.Germline breast cancer susceptibility gene mutations and breast cancer outcomes.Functional Interaction Between and DNA Repair in Yeast May Uncover a Role of , and Somatic Variants in Cancer Development

P2860

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P2860

Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

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