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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

2. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

3. Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

4. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

5. Genetic diversity fuels gene discovery for tobacco and alcohol use

6. Common Genetic Variation and Age of Onset of Anorexia Nervosa.

7. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.

8. HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases

9. Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

10. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

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

14. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

15. Rare coding variants in ten genes confer substantial risk for schizophrenia.

16. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.

17. Resource profile and user guide of the Polygenic Index Repository

18. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

20. Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders

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

22. Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

25. Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation

26. Comorbidities confound metabolomics studies of human disease

27. Genome-wide association study identifies 48 common genetic variants associated with handedness

28. Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies

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

30. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

31. A saturated map of common genetic variants associated with human height

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

34. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

35. Genetic assessment of efficacy and safety profiles of coagulation cascade proteins identifies Factors II and XI as actionable anticoagulant targets

37. Mendelian randomization prioritizes abdominal adiposity as an independent causal factor for liver fat accumulation and cardiometabolic diseases

39. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

40. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

43. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

44. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

45. Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

46. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

47. Identifying the Common Genetic Basis of Antidepressant Response

48. Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records.

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

50. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

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