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1. Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing data

2. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

3. Age-And tumor subtype-specific breast cancer risk estimates for CHEK2∗1100delC Carriers

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

5. Next-generation sequencing-based genome diagnostics across clinical genetics centers: Implementation choices and their effects

6. Genomic profiling of CHEK2*1100delC-mutated breast carcinomas

7. Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes

8. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

9. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

10. MicroRNA related polymorphisms and breast cancer risk

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

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

13. Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated

14. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

15. Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

16. CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women

17. Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

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