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3. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

7. Analysis of shared heritability in common disorders of the brain

8. Analysis of shared heritability in common disorders of the brain

9. Homozygous microdeletion of exon 5 in znf277 in a girl with specific language impairment

10. Lack of replication of previous autism spectrum disorder GWAS hits in European populations

11. Lack of replication of previous autism spectrum disorder GWAS hits in European populations

15. Reply to pembrey et al: 'Znf277 microdeletions, specific language impairment and the meiotic mismatch methylation (3m) hypothesis'

16. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

17. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

18. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

19. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

20. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

21. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

22. A genome-wide scan for common alleles affecting risk for autism

23. A genome-wide scan for common alleles affecting risk for autism

24. Functional impact of global rare copy number variation in autism spectrum disorders

25. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

26. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

29. Individual common variants exert weak effects on the risk for autism spectrum disorders

30. A genome-wide scan for common alleles affecting risk for autism

32. Short communication DNA variants in the human RAB3A gene are not associated with autism.

33. Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients

34. ELMOD3 ‐ SH2D6 gene fusion as a possible co‐star actor in autism spectrum disorder scenario

35. An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder

36. The role of rare compound heterozygous events in autism spectrum disorder

37. Analysis of shared heritability in common disorders of the brain

38. Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment

39. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

40. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

41. Analysis of X chromosome inactivation in autism spectrum disorders

42. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample

43. Individual common variants exert weak effects on the risk for autism spectrum disorderspi

44. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

45. A genome-wide scan for common alleles affecting risk for autism

46. Linkage and candidate gene studies of autism spectrum disorders in European populations

47. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

48. Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment

49. Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations

50. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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