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

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

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

4. A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

5. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival

6. Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification

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

8. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

9. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

10. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

11. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

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

13. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

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

15. Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults

16. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis

17. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

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

19. Rare germline copy number variants (CNVs) and breast cancer risk

20. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

21. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

22. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.

23. Genetic insights into biological mechanisms governing human ovarian ageing

24. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

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

26. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association ConsortiumBreast Cancer Risk Factors and Survival By Tumor Subtype

27. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.

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

29. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

30. Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

32. Mosaic Chromosomal Alterations Are Associated With Increased Lung Cancer Risk: Insight From the INTEGRAL-ILCCO Cohort Analysis

33. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

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

36. The PANcreatic Disease ReseArch (PANDoRA) consortium: Ten years’ experience of association studies to understand the genetic architecture of pancreatic cancer

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

38. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

39. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

40. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

41. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.

42. Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility.

43. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

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

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

50. Two truncating variants in FANCC and breast cancer risk.

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