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1. Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus.

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

3. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

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

6. Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

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

8. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

9. Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies

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

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

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

20. Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal

24. Hearing loss

25. Contributors

26. IBS clinical management in Italy: The AIGO survey

28. Multi-risk Assessment as a Tool for Decision-Making

29. Urbanisation and Climate Change in Africa: Setting the Scene

30. Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

33. Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA‐A*03:01 allele

38. 50 shades of lockdown: sex workers' hidden world during COVID pandemic.

41. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

43. Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

44. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

45. 19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference

46. Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment

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

50. Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment

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