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3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

9. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

12. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

13. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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

15. New insights into the genetic etiology of Alzheimer’s disease and related dementias

16. Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping

24. Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

25. "Prion-like" seeding and propagation of oligomeric protein assemblies in neurodegenerative disorders.

26. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

30. α-Synuclein strains target distinct brain regions and cell types

33. Mosaic loss of chromosome Y in leukocytes matters

38. Consensus guidelines for lumbar puncture in patients with neurological diseases

41. Altered amyloid-β structure markedly reduces gliosis in the brain of mice harboring the Uppsala APP deletion.

42. Validation of a web-based self-administered test for cognitive assessment in a Swedish geriatric setting.

45. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

47. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

48. Genetic Associations between Modifiable Risk Factors and Alzheimer Disease

49. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

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