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295 results on '"Gasparini, Paolo"'

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

2. Additional file 1 of Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population

3. Are taste variations associated with the liking of sweetened and unsweetened coffee?

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

5. Narrow-sense heritability estimation of complex traits using identity-by-descent information

6. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

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

8. Rare and low-frequency coding variants alter human adult height

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

10. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

11. Additional file 2: of Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

13. Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss

14. Trans-ethnic meta-analysis of white blood cell phenotypes

15. MOESM2 of Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations

16. MOESM1 of Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations

17. Uncertainty In The Shale Gas Debate: Views From The Science–Policymaking Interface

18. A pochi secondi dal sisma

22. Sordità

24. The spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis

25. CONNEXINS

30. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families

31. Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3

33. 'Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder'

41. Cystinuria

42. Genetica delle sordita’ non sindromiche

43. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

47. 'Suppression of CDAII expression in a homozygote'

48. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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