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1. Intervention Services for Autistic Adults:An ASDEU Study of Autistic Adults, Carers, and Professionals' Experiences

2. Mental Health in times of COVID-19: Policy Brief

3. Efficacy of focused social and communication intervention practices for young children with autism spectrum disorder: A meta-analysis

4. Exposure to Xenobiotics and Gene-Environment Interactions in Autism Spectrum Disorder: A Systematic Review

5. Real-World Experiences in Autistic Adult Diagnostic Services and Post-diagnostic Support and Alignment with Services Guidelines: Results from the ASDEU Study

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

7. Definition of a putative pathological region in PARK2 associated with autism spectrum disorder through in silico analysis of its functional structure

8. Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning

9. Network Propagation-Based Semi-supervised Identification of Genes Associated with Autism Spectrum Disorder

10. Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives

11. FunVar: A systematic pipeline to unravel the convergence patterns of genetic variants in ASD, a paradigmatic complex disease

12. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

13. A role for gene-environment interactions in Autism Spectrum Disorder is suggested by variants in genes regulating exposure to environmental factors

14. Identifying disease genes using machine learning and gene functional similarities, assessed through Gene Ontology

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

16. Attitudes of the autism community to early autism research

17. Variants in the Inflammatory IL6 and MPO Genes Modulate Stroke Susceptibility Through Main Effects and Gene—Gene Interactions

18. Association of a Genetic Variant in the ALOX5AP with Higher Risk of Ischemic Stroke: A Case-Control, Meta-Analysis and Functional Study

19. A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

20. Use of early intervention for young children with autism spectrum disorder across Europe

21. Mitochondrial dysfunction in autism spectrum disorders: a population-based study

22. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels

23. Brief Report: High Frequency of Biochemical Markers for Mitochondrial Dysfunction in Autism: No Association with the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene

24. Autoantibody repertoires to brain tissue in autism nuclear families

25. [Untitled]

26. Evidence for epistatic gene interactions between growth factor genes in stroke outcome

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

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

29. The Autism Simplex Collection : an international, expertly phenotyped autism sample for genetic and phenotypic analyses

30. Protein interaction networks reveal novel autism risk genes within GWAS statistical noise

31. NCAM and schizophrenia: genetic studies

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

33. Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders

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

35. Compensatory T-Cell Regulation in Unaffected Relatives of SLE Patients, and Opposite IL-2/CD25-Mediated Effects Suggested by Coreferentiality Modeling

36. TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approaches

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

38. Variants within the nitric oxide synthase 1 gene are associated with stroke susceptibility

39. Replication of the CELSR1 association with ischemic stroke in a Portuguese case-control cohort

40. Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism

41. Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after stroke

42. Kalirin: a novel genetic risk factor for ischemic stroke

43. Pharmacogenetics of risperidone therapy in autism: association analysis of eight candidate genes with drug efficacy and adverse drug reactions

44. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies

45. A genome-wide linkage and association scan reveals novel loci for autism

46. Association of the alpha4 integrin subunit gene (ITGA4) with autism

47. Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFβ gene variants

48. A remarkable depletion of both naïve CD4+ and CD8+ with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain

49. Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients

50. Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions

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