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249 results on '"Caldés, Trinidad"'

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1. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

2. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

3. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

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

5. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

6. Genome-wide association study of germline variants and breast cancer-specific mortality

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

8. Publisher Correction: Shared heritability and functional enrichment across six solid cancers

9. Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing

10. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

11. Shared heritability and functional enrichment across six solid cancers

13. The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

14. Association analysis identifies 65 new breast cancer risk loci

15. BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study

16. Prognostic Value of BRAF, PI3K, PTEN, EGFR Copy Number, Amphiregulin and Epiregulin Status in Patients with KRAS Codon 12 Wild-Type Metastatic Colorectal Cancer Receiving First-Line Chemotherapy with Anti-EGFR Therapy

19. Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers

22. Variation in the Risk of Colorectal Cancer for Lynch Syndrome: A retrospective family cohort study

24. Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their origin

27. Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer

28. Evidence for a link between TNFRSF11A and risk of breast cancer

30. International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation

31. Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriers

32. Comprehensive annotation of splice junctions supports pervasive alternative splicing at the BRCA1 locus: a report from the ENIGMA consortium

33. Association of MUTYH and MSH6 germline mutations in colorectal cancer patients

34. About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants

38. Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 (FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles

40. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

41. Characterization of the cancer spectrum in men with germline BRCA1 and BRCA2 pathogenic variants

42. Alcohol consumption, cigarette smoking, and risk of breast cancer for BRCA1 and BRCA2 mutation carriers: results from The BRCA1 and BRCA2 Cohort Consortium

46. Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

47. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)

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