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207 results on '"Génétique humaine et Fonctions cognitives - Human Genetics and Cognitive Functions"'

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1. From clinic to the 'foul and exciting field of life': A psychiatric point of view on clinical physiology

2. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

3. Associations of the Intellectual Disability Gene MYT1L with Helix–Loop–Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval

4. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions

5. Inpatient target discharge weight for early-onset anorexia nervosa: Restoring premorbid BMI percentile to improve height prognosis

6. Impact of the gut microbiome on nicotine’s motivational effects and glial cells in the ventral tegmental area in male mice

7. The Link Between Autism and Sex-Related Neuroanatomy, and Associated Cognition and Gene Expression

8. The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation

9. The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disorders

10. Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas

11. Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome

12. Phenotypic effects of genetic variants associated with autism

13. Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders

14. A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

15. Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

16. Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome

17. Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism

18. Consensus recommendations on Epilepsy in Phelan-McDermid syndrome

19. Characterization of Incomplete Hippocampal Inversions in a large dataset of young healthy subjects

20. Common genetic variants influence human subcortical brain structures

21. Neuropsychiatry

22. Chapeau UK Biobank! A revolution for integrated research on humans and large-scale data sharing

23. Neurobiological Correlates of Change in Adaptive Behavior in Autism

24. Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder

25. Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways

26. Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure

27. Processing of social and monetary rewards in autism spectrum disorders

28. Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry

29. Excessive self-grooming of $Shank3$ mutant mice is associated with gene dysregulation and imbalance between the striosome and matrix compartments in the striatum

30. A 16p11.2 deletion mouse model displays quantitatively and qualitatively different behaviours in sociability and social novelty over short- and long-term observation

31. Humanized Chimeric Mouse Models to Study Human Neural Development and Pathogenesis of Brain Diseases

32. Structural and functional brain alterations revealed by neuroimaging in CNV carriers

33. Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares

34. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

35. 10q26 deletion syndrome: a French cohort study

36. Resting state EEG power spectrum and functional connectivity in autism: a cross-sectional analysis

37. Sub-diagnostic effects of genetic variants associated with autism

38. Brain charts for the human lifespan

39. Dark control: The default mode network as a reinforcement learning agent

40. Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

41. Do not Dispose of Historic Fluid Collections: Evaluating Research Potential and Range of Use

42. Deep learning-based system for real-time behavior recognition and closed-loop control of behavioral mazes using depth sensing

43. The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions

44. Stratifying the autistic phenotype using electrophysiological indices of social perception

45. Early Systemic Inflammation Induces Neurodevelopmental Disorders: Results from Artemis, a French Multicenter Study of Juvenile Rheumatisms and Systemic Autoimmune and Auto-Inflammatory Disorders and Meta-Analysis

46. Machine learning for neurodevelopmental disorders

47. Phelan-McDermid syndrome: a classification system after 30 years of experience

48. Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series

49. The meaning of significant mean group differences for biomarker discovery

50. Cell-type- and region-specific modulation of cocaine seeking by micro-RNA-1 in striatal projection neurons

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