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32 results on '"Perttu Salo"'

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1. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

2. The genomics of heart failure: design and rationale of the HERMES consortium

3. Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

4. High-sensitivity cardiac troponin I and NT-proBNP as predictors of incident dementia and Alzheimer’s disease: the FINRISK Study

5. Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

6. A multivariate linear model for investigating the association between gene-module co-expression and a continuous covariate

7. Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases

8. A distinctive DNA methylation pattern in insufficient sleep

9. Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome

10. Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications

11. Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population

12. Evaluation of HLA-DRB1 imputation using a Finnish dataset

13. On the Combination of Omics Data for Prediction of Binary Outcomes

14. Thyroid cancer and co-occurring RET mutations in Hirschsprung disease

15. Apolipoproteins and HDL cholesterol do not associate with the risk of future dementia and Alzheimer's disease: the National Finnish population study (FINRISK)

16. Evaluation of O2PLS in Omics data integration

17. The Detection of Metabolite-Mediated Gene Module Co-Expression Using Multivariate Linear Models

18. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

19. Patient Overcrowding in Hospital Wards as a Predictor of Diagnosis-Specific Mental Disorders Among Staff

20. Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population

21. Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

22. A RISK LOCUS FOR NON-ST-ELEVATION MYOCARDIAL INFARCTION ON CHROMOSOME 1P13.3 IS ALSO ASSOCIATED WITH PERIPHERAL ARTERY DISEASE IN PATIENTS WITH ACUTE CORONARY SYNDROME

23. A metabolic view on menopause and ageing

24. Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture

25. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

26. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

27. Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure

28. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

29. Comparison of solution-based exome capture methods for next generation sequencing

30. Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

31. Identification of seven loci affecting mean telomere length and their association with disease

32. Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

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