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

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

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

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

7. A Multi-View Deep Evidential Learning Approach for Mammogram Density Classification

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

35. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

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

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

42. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

43. Author Correction: Palaeogenomics of Upper Palaeolithic to Neolithic European hunter-gatherers

44. Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

45. 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

46. The debatable presence of PIWI‐interacting RNAs in invasive breast cancer

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

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