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

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

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

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

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

12. Association analysis identifies 65 new breast cancer risk loci

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

15. 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

17. 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

20. 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

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

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

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

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

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

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

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

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

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

43. Exploring the link between MORF4L1 and risk of breast cancer

44. Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).

45. Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer.

46. Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report.

47. RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibility.

48. Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.

49. Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes.

50. BRCA2 gene mutations and coagulation-associated biomarkers.

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