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1. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

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

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. Markers of imminent myocardial infarction

5. Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank

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

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

8. Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

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

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

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

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

14. A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

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

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

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

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

20. The genetic architecture of sporadic and multiple consecutive miscarriage.

21. Personalized early detection and prevention of breast cancer: ENVISION consensus statement

22. Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement

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

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

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

26. A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

27. Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

28. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

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

30. The PROPHET project paves the way for personalized prevention in the future healthcare

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

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

34. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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

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

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

40. Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review

41. Identifying the Common Genetic Basis of Antidepressant Response

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

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

45. Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

46. Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

47. Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants

48. Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

49. Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

50. Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts

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