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337 results on '"Kaunisto, Mari A."'

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

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

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

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

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

6. Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

8. Transforming science communication through storytelling.

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

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

12. HMG-CoA reductase is a potential therapeutic target for migraine:a mendelian randomization study

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

14. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

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

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

19. A second update on mapping the human genetic architecture of COVID-19

24. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

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

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

30. Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

32. Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

33. sj-pdf-2-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

34. sj-pdf-7-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

35. sj-pdf-1-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

36. sj-pdf-3-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

37. sj-pdf-5-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

38. sj-pdf-6-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

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

40. sj-pdf-1-cep-10.1177_03331024211045651 - Supplemental material for Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

41. Migreenin geneettinen tausta on monitekijäinen

42. Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults

43. Mapping the human genetic architecture of COVID-19

44. Consistently replicating locus linked to migraine on 10q22-q23

45. Cerebral small vessel disease genomics and its implications across the lifespan

46. Cerebral small vessel disease genomics and its implications across the lifespan

47. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

49. Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults

50. A susceptibility locus for migraine with aura, on chromosome 4q24

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