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1. Defining the role of common variation in the genomic and biological architecture of adult human height

2. Causal effect of plasminogen activator inhibitor type 1 on coronary heart disease

3. Biological interpretation of genome-wide association studies using predicted gene functions

4. Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension

5. 237 Ischaemic stroke in systemic lupus erythematosus, -distribution of subtypes and a risk genotype in the stat4 gene

6. Genetically Determined Height and Coronary Artery Disease

7. The Lin28/let-7 axis regulates glucose metabolism

8. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

9. Genome-wide association study identifies eight loci associated with blood pressure

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

11. Biological interpretation of genome-wide association studies using predicted gene functions

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

13. Genetically determined height and coronary artery disease

14. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

15. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

16. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

17. Genome sequence, comparative analysis and population genetics of the domestic horse (Equus caballus)

18. Genome-wide association study identifies eight loci associated with blood pressure

19. The role of adiposity in cardiometabolic traits: a mendelian randomization analysis

20. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.

21. Genetic Loci for Retinal Arteriolar Microcirculation

28. Estrogen receptor alpha gene polymorphism and endometrial cancer risk--a case-control study.

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

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

31. A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

32. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women

33. Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

34. Unraveling the Genetics of Shared Clinical and Serological Manifestations in Patients With Systemic Inflammatory Autoimmune Diseases.

35. Multimodal Single-Cell Sequencing of B Cells in Primary Sjögren's Syndrome.

36. Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia.

37. Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies.

38. Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia.

39. Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases.

40. Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus.

41. Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia.

42. DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren's Syndrome.

43. Variants in BANK1 are associated with lupus nephritis of European ancestry.

44. Contributions of de novo variants to systemic lupus erythematosus.

45. Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing.

46. Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.

47. Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced Angioedema.

48. Association of aberrant ASNS imprinting with asparaginase sensitivity and chromosomal abnormality in childhood BCP-ALL.

49. Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling.

50. Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia.

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