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1. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

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

3. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

4. A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

5. Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

6. The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

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

8. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

9. Identification of risk loci for primary aldosteronism in genome-wide association studies

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

12. Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

13. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

14. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

15. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

16. Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer”

17. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.

18. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.

19. Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients

20. Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

21. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

22. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

23. α- and β-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy

24. alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy.

25. Dissecting the genetic heterogeneity of gastric cancer

26. Associations of autozygosity with a broad range of human phenotypes

28. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

29. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

30. Association of colorectal cancer with genetic and epigenetic variation in PEAR1-A population-based cohort study

33. Supplement to: Genetic drivers of kidney defects in the DiGeorge syndrome.

34. Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy

35. Genome-wide association study identifies 74 loci associated with educational attainment

36. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

37. Association of colorectal cancer with genetic and epigenetic variation in PEAR1—A population-based cohort study

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

39. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

40. Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide

41. Risk of nephrolithiasis in primary hyperparathyroidism is associated with two polymorphisms of the calcium-sensing receptor gene

42. Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

44. Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components

45. GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy

46. Genome-wide association study identifies new locus associated with OCD

47. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

50. Directional dominance on stature and cognition in diverse human populations

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