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60 results on '"Mervi Aavikko"'

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1. Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure

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

3. Sex-specific familial aggregation of cancers in Finland

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

5. Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

6. Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

7. Contribution of allelic imbalance to colorectal cancer

8. Comprehensive evaluation of coding region point mutations in microsatellite‐unstable colorectal cancer

9. Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity

10. Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12.

11. Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcoma.

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

13. Supplementary Table 5 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

14. Supplementary Table 3 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

15. Supplementary Table 7 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

16. Supplementary Table 1 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

17. Supplementary Figures 1-19, supplementary methods and extended literature evaluation of the candidate genes from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

18. Supplementary Table 6 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

19. Supplementary Table 4 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

20. Supplementary Table 2 from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

21. Data from Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

22. New insights into the genetic etiology of Alzheimer's disease and related dementias

23. Next-generation sequencing in a large pedigree segregating visceral artery aneurysms suggests potential role of COL4A1/COL4A2 in disease etiology

24. FinnGen: Unique genetic insights from combining isolated population and national health register data

25. Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease-Associated Colorectal Cancer

26. WNT2 activation through proximal germline deletion predisposes to small intestinal neuroendocrine tumors and intestinal adenocarcinomas

27. Germline mutations in young non-smoking women with lung adenocarcinoma

28. Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

29. Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing

30. Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

31. Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers

32. Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

33. Comprehensive evaluation of coding region point mutations in microsatellite-unstable colorectal cancer

34. Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

35. Contribution of allelic imbalance to colorectal cancer

36. Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

37. Candidate susceptibility variants for esophageal squamous cell carcinoma

38. Accumulation of genomic alterations in 2p16, 9q33.1 and 19p13 in lung tumours of asbestos-exposed patients

39. MED12 , the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

40. Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma

41. Abstract LB-382: Identification of predisposing genes for small bowel adenocarcinoma by exome sequencing

42. DNA copy number loss and allelic imbalance at 2p16 in lung cancer associated with asbestos exposure

43. 3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity

44. Whole-Genome Sequencing Identifies STAT4 as a Putative Susceptibility Gene in Classic Kaposi Sarcoma

45. Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity

46. Clinical characterization, genetic mapping and whole-genome sequence analysis of a novel autosomal recessive intellectual disability syndrome

47. Primary mediastinal large B-cell lymphoma segregating in a family: exome sequencing identifies MLL as a candidate predisposition gene

48. Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcoma

49. Abstract 4435: Genome-scale DNA methylation changes delineate uterine leiomyoma subgroups

50. Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

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