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

2. Genome-wide characterization of circulating metabolic biomarkers

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

5. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

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

7. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

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

9. Genetic insights into resting heart rate and its role in cardiovascular disease

11. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

12. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.

13. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

14. Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

15. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

16. Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

17. Association of structural variation with cardiometabolic traits in Finns

18. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

19. Large-scale association analyses identify host factors influencing human gut microbiome composition

20. Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations

21. Identification of type 2 diabetes loci in 433,540 East Asian individuals

22. Complement genes contribute sex-biased vulnerability in diverse disorders.

23. Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.

24. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

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

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

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

29. ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition—implications for COVID-19

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

31. Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.

32. New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

33. Exome sequencing of Finnish isolates enhances rare-variant association power

34. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

35. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

36. Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease

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

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

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

40. The HUNT study: A population-based cohort for genetic research

41. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

42. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

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

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

45. Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

46. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

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

48. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

50. The power of genetic diversity in genome-wide association studies of lipids

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