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Your search keyword '"Peysselon M."' showing total 14 results

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14 results on '"Peysselon M."'

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1. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

2. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

3. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

4. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

5. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

6. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

7. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

8. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

9. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

10. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

11. Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes.

13. BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management.

14. A novel POLD1 pathogenic variant identified in two families with a cancer spectrum mimicking Lynch syndrome.

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