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1. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

2. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

3. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

4. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1

5. Prediction of breast cancer risk based on profiling with common genetic variants

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

7. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

8. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

9. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

10. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

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

12. 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

13. Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 (CIMBA)

14. Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies

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