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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

2. Disentangling the relationships of body mass index and circulating sex hormone concentrations in mammographic density using Mendelian randomization

4. Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel

5. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

10. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

12. Risks of second primary cancers among 584,965 female and male breast cancer survivors in England: a 25-year retrospective cohort study

14. Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

15. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

18. Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families

20. Improving reporting standards for polygenic scores in risk prediction studies

21. Personalized early detection and prevention of breast cancer: ENVISION consensus statement

22. Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement

23. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

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

26. BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry

27. Cancer incidence and competing mortality risk following 15 presenting symptoms in primary care: a population-based cohort study using electronic healthcare records

28. Breast cancer risk assessment for prescription of Menopausal Hormone Therapy in women who have a family history of breast cancer

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

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

33. Shared heritability and functional enrichment across six solid cancers.

35. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

36. Overlap of high-risk individuals predicted by family history, and genetic and non-genetic breast cancer risk prediction models: implications for risk stratification

37. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

38. Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study.

39. Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families

40. Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction

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

44. Implementing Multifactorial Risk Assessment with Polygenic Risk Scores for Personalized Breast Cancer Screening in the Population Setting: Challenges and Opportunities.

45. Immune Cell Associations with Cancer Risk

46. Age- and Tumor Subtype–Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

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

48. Genetics, primary care records and lifestyle factors for short-term dynamic risk prediction of colorectal cancer: prospective study of asymptomatic and symptomatic UK Biobank participants

49. Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey

50. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

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