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1. Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition

2. Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility

3. Hereditary predisposition to breast cancer:evaluating the role of rare candidate alleles discovered by whole-exome sequencing

4. Optical genome mapping as an alternative to FISH-based cytogenetic assessment in chronic lymphocytic leukemia

5. ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways:lessons from breast cancer patients

6. Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility

7. Uudet long-read-teknologiat:kohti tarkennettua genomitietoa perinnöllisistä sairauksista ja syövistä

8. ATM c.7570G>C is a high-risk allele for breast cancer

9. A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

10. Genetic variants associated with sudden cardiac death in victims with single vessel coronary artery disease and left ventricular hypertrophy with or without fibrosis

11. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

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

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

14. Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims

15. Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer

16. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

17. Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition

18. Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders

19. BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells

20. Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly

21. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

22. Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer

23. The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

24. Machine learning identifies interacting genetic variants contributing to breast cancer risk:a case study in Finnish cases and controls

25. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

26. The BRCA2 c.68‐7T > A variant is not pathogenic:a model for clinical calibration of spliceogenicity

27. Hereditary predisposition to breast cancer:evaluating the role of rare copy number variant, protein-truncating and missense candidate alleles

28. DNA damage response gene mutations and inherited susceptibility to breast cancer

29. FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population

30. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

31. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes

32. ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer

33. Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer

34. BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer

35. Hereditary predisposition to breast cancer:evaluating the role of rare candidate alleles discovered by whole-exome sequencing

36. Hereditary predisposition to breast cancer:evaluating the role of rare copy number variant, protein-truncating and missense candidate alleles

37. DNA damage response gene mutations and inherited susceptibility to breast cancer

38. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes

39. Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer

40. BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer

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