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

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

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

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

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

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

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

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

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

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

27. NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

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

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

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

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

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

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

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

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

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

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

39. Migreenin geneettinen tausta on monitekijäinen

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

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

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

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

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

46. Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons

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

49. Analysis of shared heritability in common disorders of the brain

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