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

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

4. Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer

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

6. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

7. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

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

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

12. Mapping the human genetic architecture of COVID-19

14. SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

15. Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

16. Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.

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

18. Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases

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

20. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

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

22. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

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

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

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

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

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

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

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

37. Genetic analyses identify widespread sex-differential participation bias

38. Fish with slow life‐history cope better with chronic manganese exposure than fish with fast life‐history.

40. Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer

42. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

43. Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan

46. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

47. New genetic loci link adipose and insulin biology to body fat distribution

48. Genetic studies of body mass index yield new insights for obesity biology

49. PAPR Constrained Power Allocation for Iterative Frequency Domain Multiuser SIMO Detector

50. Convergence Constrained Multiuser Transmitter-Receiver Optimization in Single Carrier FDMA

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