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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

7. Bronze age Northern Eurasian genetics in the context of development of metallurgy and Siberian ancestry

9. Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies

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

11. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

13. Nuclei instance segmentation from histopathology images using Bayesian dropout based deep learning

14. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

15. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases

17. A FinnGen pilot clinical recall study for Alzheimer’s disease

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

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

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

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

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

23. A FinnGen pilot clinical recall study for Alzheimer’s disease

24. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

25. 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

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

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

28. Palaeogenomics of Upper Palaeolithic to Neolithic European hunter-gatherers

29. FinnGen provides genetic insights from a well-phenotyped isolated population

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

31. 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

32. Histone demethylase GASC1 - a potential prognostic and predictive marker in invasive breast cancer

33. SULT1A1 rs9282861 polymorphism-a potential modifier of efficacy of the systemic adjuvant therapy in breast cancer?

34. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

35. Twist and snai1 expression in pharyngeal squamous cell carcinoma stroma is related to cancer progression

36. Transcription factors zeb1, twist and snai1 in breast carcinoma

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

38. 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?

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

40. Nuclear expression of Snail1 in borderline and malignant epithelial ovarian tumours is associated with tumour progression

41. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

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

44. High Numbers of CD163+ Tumor-Associated Macrophages Predict Poor Prognosis in HER2+ Breast Cancer

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

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

47. Expression profiles of small non-coding RNAs in breast cancer tumors characterize clinicopathological features and show prognostic and predictive potential

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

49. Area-based breast percentage density estimation in mammograms using weight-adaptive multitask learning

50. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

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