Search

Your search keyword '"Priit Palta"' showing total 98 results

Search Constraints

Start Over You searched for: Author "Priit Palta" Remove constraint Author: "Priit Palta"
98 results on '"Priit Palta"'

Search Results

1. High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

2. Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations

3. Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation

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

5. Genetic causal relationship between immune diseases and migraine: a Mendelian randomization study

6. Targeted gene expression profiling for accurate endometrial receptivity testing

7. Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

8. Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

9. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

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

11. The role of polygenic risk and susceptibility genes in breast cancer over the course of life

12. Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples.

13. Sleep apnoea is a risk factor for severe COVID-19

14. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

15. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

16. Computational framework for targeted high-coverage sequencing based NIPT.

17. Haplotype phasing and inheritance of copy number variants in nuclear families.

18. Distribution and medical impact of loss-of-function variants in the Finnish founder population.

19. A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling.

20. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

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

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

24. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

25. BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples

27. Targeted gene expression profiling for accurate endometrial receptivity testing

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

29. Global Biobank Meta-analysis Initiative: powering genetic discovery across human diseases

30. Primary age-related tauopathy in a Finnish population-based study of the oldest old (Vantaa 85+)

31. Association and genetic overlap between clinical chemistry tests and migraine

32. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

33. GWAS meta-analysis and gene expression data link reproductive tract development, immune response and cellular proliferation/apoptosis with cervical cancer and clarify overlap with other cervical phenotypes

34. Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting

35. Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

36. Genetic variant in SPDL1 reveals novel mechanism linking pulmonary fibrosis risk and cancer protection

37. Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

38. Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

39. Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

40. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

41. High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

42. Polygenic Hyperlipidemias and Coronary Artery Disease Risk

43. Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers

44. An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

45. An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

46. NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies

47. Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

48. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

49. Polygenic Hyperlipidemias and Coronary Artery Disease Risk

50. Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers

Catalog

Books, media, physical & digital resources