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545 results on '"Kuusisto, J"'

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1. Evaluation of the efficacy and safety of three dosing regimens of agalsidase alfa enzyme replacement therapy in adults with Fabry disease

3. Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

4. Novel biomarkers associated with incident heart failure in 10 106 Finnish men

8. A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

10. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x)

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

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

35. Radionuclide image in chronic heart failure oral abstract session

36. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 26, 2018)

37. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017)

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

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

40. A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression

41. A partial loss-of-function variant in AKT2 is associated with reduced insulin-mediated glucose uptake in multiple insulin-sensitive tissues: A genotype-based callback positron emission tomography study

42. Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

43. Structural immaturity of human iPSC-derived cardiomyocytes:in silico investigation of effects on function and disease modeling

46. Genetic risk scores in the prediction of plasma glucose, impaired insulin secretion, insulin resistance and incident type 2 diabetes in the METSIM study

47. Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

48. Radionuclide image in chronic heart failure oral abstract session

49. Genetically Determined Height and Coronary Artery Disease

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