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111 results on '"Pharoah, Paul D.P."'

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1. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

2. Elucidating the Risk of Colorectal Cancer for Variants in Hereditary Colorectal Cancer Genes

3. The impact of coding germline variants on contralateral breast cancer risk and survival

4. No Association Between Polygenic Risk Scores for Cancer and Development of Radiation Therapy Toxicity

5. Segregation analysis of 17,425 population-based breast cancer families: Evidence for genetic susceptibility and risk prediction

6. Incorporating progesterone receptor expression into the PREDICT breast prognostic model

7. Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects

9. Refined cut-off for TP53 immunohistochemistry improves prediction of TP53 mutation status in ovarian mucinous tumors: implications for outcome analyses

10. A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases

11. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

12. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women

13. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

15. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

16. Evaluating the ovarian cancer gonadotropin hypothesis: A candidate gene study

17. A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity

19. Gene–environment interactions involving functional variants: Results from the Breast Cancer Association Consortium

20. Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival.

23. Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

24. Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

25. Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

26. Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

27. Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

28. A tumor DNA complex aberration index is an independent predictor of survival in breast and ovarian cancer

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

30. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

31. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

32. Consortium analysis of gene and gene–folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

34. A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium

35. Polygenes, risk prediction, and targeted prevention of breast cancer

36. Breast cancer risks for BRCA 1/2 carriers

37. Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls

39. The role of genetic breast cancer susceptibility variants as prognostic factors

40. 11q13 Is a Susceptibility Locus for Hormone Receptor Positive Breast Cancer

41. Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study

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

43. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium

44. Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk

45. Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer

46. Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study

48. Association of ESR1 gene tagging SNPs with breast cancer risk

49. Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer

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