Associated Papers
Multiple Myeloma Risk and Outcomes Are Associated with Pathogenic Germline Variants in DNA Repair Genes.
Thibaud S et al.
Blood Cancer Discovery, 2024
Association of XRCC2 with breast cancer, a multi-omics analysis at genomic, transcriptomic, and epigenomic level.
Gilani N et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2024
Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers.
Golmard L et al.
European Journal of Human Genetics : Ejhg, 2017
A Review of Whole-Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery.
Chandler MR et al.
Human Mutation, 2016
Functional Analysis of Missense Variants in the Putative Breast Cancer Susceptibility Gene XRCC2.
Hilbers FS et al.
Human Mutation, 2016
Multigene testing of moderate-risk genes: be mindful of the missense.
Young EL et al.
Journal of Medical Genetics, 2016
26787654 (PubMed )
Supplement: jmedgenet-2015-103398-s2.pdf
Rare mutations in XRCC2 increase the risk of breast cancer.
Park DJ et al.
American Journal of Human Genetics, 2012
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