172 results on '"Chaste, Pauline"'
Search Results
2. Auditory illusions and Post-traumatic stress disorder: Sound test in a case-control study
3. The Bulle: Support and Prevention of Psychological Decompensation of Health Care Workers During the Trauma of the COVID-19 Epidemic
4. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
5. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
6. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
7. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.
8. Common genetic variants, acting additively, are a major source of risk for autism.
9. Preliminary Psychometric Properties of the Autism Mental Status Examination (AMSE) in a Tertiary Care Center for Autism Spectrum Disorder Diagnosis
10. Feelings of regret and disappointment in adults with high-functioning autism
11. Episodic memory and self-awareness in Asperger Syndrome: Analysis of memory narratives
12. Architecture of the Genetic Risk for Autism
13. From Autism to Autism Spectrum Disorders
14. Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation
15. The role of causal and intentional judgments in moral reasoning in individuals with high functioning autism
16. Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders
17. Analysis of X chromosome inactivation in autism spectrum disorders
18. Genetic and Functional ascertainment of the Melatonin Pathway in Patients with Attention Deficit and Hyperactivity Disorders
19. High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
20. Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
21. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
22. Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders
23. An investigation of ribosomal protein L10 gene in autism spectrum disorders
24. Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
25. Link between Neurodevelopmental Disorders and Suicidal Risk in Children
26. Parental involvement and adjustment during the diagnostic evaluation of autism spectrum disorder at two diagnostic centers
27. Telepsychiatry for Children and Adolescents: A Review of the PROMETTED Project
28. Risque d’autisme : une architecture complexe
29. The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability
30. Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders
31. Microdeletions of ELP4 are associated with language impairment, autism spectrum disorder and epilepsy
32. Microdeletions ofELP4Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation
33. [Alterations in synapsis formation and function in autism disorders]
34. On the Neuroimaging of Autism in the Context of Human Brain Diversity
35. Individuals with Autism Spectrum Disorders Do Not Use Social Stereotypes in Irony Comprehension
36. Autism risk factors: genes, environment, and gene-environment interactions
37. The Role of Causal and Intentional Judgments in Moral Reasoning in Individuals with High Functioning Autism
38. Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
39. Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
40. Memory for Self-Performed Actions in Individuals with Asperger Syndrome
41. Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
42. Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population
43. Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
44. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
45. Reduced 3-O -methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele
46. Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
47. Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders
48. Predictors of Treatment Response in Pediatric Obsessive-Compulsive Disorder
49. An investigation of ribosomal protein L10 gene in autism spectrum disorders
50. Identification d’une voie synaptique associée à l’autisme
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