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24 results on '"Kurra, Venla"'

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1. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

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

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

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

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

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

7. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

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

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

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

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

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

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

16. Leveraging Northern European population history : novel low-frequency variants for polycystic ovary syndrome

17. Moderate hyperuricaemia ameliorated kidney damage in a low‐renin model of experimental renal insufficiency.

18. Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome.

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

20. Effects of oxonic acid-induced hyperuricemia on mesenteric artery tone and cardiac load in experimental renal insufficiency

23. Hyperuricemia, Oxidative Stress, and Carotid Artery Tone in Experimental Renal Insufficiency.

24. Broadening the Phenotype Spectrum of MECP2 Variants in Men.

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