1,201 results on '"Bourgeron, Thomas"'
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2. Le projet gnomAD montre l’importance de ne pas avoir qu’un seul génome humain de référence !
3. Effectiveness of a positive psychology and mindfulness-based app on mental health for parents of children with a neurodevelopmental disorder: study protocol of a pragmatic international randomized controlled trial
4. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
5. Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry.
6. From Symptomatology to Functioning - Applying the ICF to Autism Measures to Facilitate Neurodiversity-Affirmative Data Harmonization
7. Phenotypic effects of genetic variants associated with autism
8. Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications
9. The neuroanatomical substrates of autism and ADHD and their link to putative genomic underpinnings
10. Fine-grained topographic organization within somatosensory cortex during resting-state and emotional face-matching task and its association with ASD traits
11. Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure
12. Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism
13. Differences in Intrinsic Gray Matter Connectivity and Their Genomic Underpinnings in Autism Spectrum Disorder
14. Autism Is Associated With Interindividual Variations of Gray and White Matter Morphology
15. Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome
16. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome
17. Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.
18. Consensus recommendations on Epilepsy in Phelan-McDermid syndrome
19. Cortico-Cerebellar neurodynamics during social interaction in Autism Spectrum Disorders
20. Genetic correlates of phenotypic heterogeneity in autism
21. European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry
22. Qualitative differences in the spatiotemporal brain states supporting configural face processing emerge in adolescence in autism
23. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.
24. Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery
25. Phelan-McDermid syndrome: a classification system after 30 years of experience
26. Differences in Intrinsic Gray Matter Connectivity and Their Genomic Underpinnings in Autism Spectrum Disorder
27. Temporal Profiles of Social Attention Are Different Across Development in Autistic and Neurotypical People
28. Atypical Brain Asymmetry in Autism—A Candidate for Clinically Meaningful Stratification
29. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
30. Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability
31. Improving heritability estimation by a variable selection approach in sparse high dimensional linear mixed models
32. A foundational atlas of autism protein interactions reveals molecular convergence
33. Detecting Central Auditory Processing Disorders in Awake Mice
34. European Autism GEnomics Registry (EAGER): Protocol for a multicentre cohort study and registry
35. LEARNING BIOLOGY FROM COMMON AND RARE VARIANT ASSOCIATIONS TO AUTISM
36. F59. DISSECTING THE CONTRIBUTIONS OF RARE AND COMMON GENETIC VARIATION TO NEURODEVELOPMENTAL OUTCOMES
37. A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder
38. Real-time analysis of the behaviour of groups of mice via a depth-sensing camera and machine learning
39. The functional database of the ARCHI project: Potential and perspectives
40. Altered Connectivity Between Cerebellum, Visual, and Sensory-Motor Networks in Autism Spectrum Disorder: Results from the EU-AIMS Longitudinal European Autism Project
41. La causalité dans les sciences biologiques et médicales
42. Chapitre 8 – L’autisme : quelles corrélations, quelles causes et quelles interventions ?
43. Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders
44. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
45. Bridge-building between communities: Imagining the future of biomedical autism research
46. Improving heritability estimation by a variable selection approach in sparse high dimensional linear mixed models
47. Behavioural Phenotypes and Neural Circuit Dysfunctions in Mouse Models of Autism Spectrum Disorder
48. Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics
49. Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
50. Individual common variants exert weak effects on the risk for autism spectrum disorders
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