Search

Your search keyword '"Moreno-De-Luca, D"' showing total 73 results

Search Constraints

Start Over You searched for: Author "Moreno-De-Luca, D" Remove constraint Author: "Moreno-De-Luca, D"
73 results on '"Moreno-De-Luca, D"'

Search Results

1. A genome-wide association study of autism using the Simons simplex collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

2. Loss of δ-catenin function in severe autism

3. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

4. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

5. Common genetic variants, acting additively, are a major source of risk for autism

8. Contributors

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

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

11. Tyrosine hydroxylase and DOPA decarboxylase gene variants in personality traits

12. Common genetic variants, acting additively, are a major source of risk for autism

14. Tyrosine hydroxylase and DOPA decarboxylase gene variants in personality traits

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

16. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

17. Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

18. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

19. Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior

21. Leveraging neuroscience education to address stigma related to opioid use disorder in the community: a pilot study.

22. Leveraging neuroscience education to address stigma related to opioid use disorder (OUD) in the community: A pilot study.

23. Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing.

24. All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders.

27. Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study.

28. Mosaic trisomy 20 and mitigation in capital crimes sentencing: A review and case report.

29. Dr Nurnberger and Colleagues Reply.

32. What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics.

34. Autism genetics: opportunities and challenges for clinical translation.

35. Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication.

37. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.

38. Loss of δ-catenin function in severe autism.

39. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.

40. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

41. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.

42. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

43. Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

44. Common genetic variants, acting additively, are a major source of risk for autism.

45. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

46. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.

47. Copy number variants: a new molecular frontier in clinical psychiatry.

48. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

49. Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.

50. Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.

Catalog

Books, media, physical & digital resources