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1. Adaptation to a changing environment: what me Normal?

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

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

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

6. A second update on mapping the human genetic architecture of COVID-19

7. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

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

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

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

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

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

14. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

15. Genomic architecture of human neuroanatomical diversity

17. Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

18. LifeTime and improving European healthcare through cell-based interceptive medicine

20. Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine (Nature, (2020), 587, 7834, (377-386), 10.1038/s41586-020-2715-9)

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

22. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

23. Abnormal melatonin synthesis in autism spectrum disorders

24. Dissecting the phenotypic heterogeneity in sensory features in autism spectrum disorder: a factor mixture modelling approach

25. Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

26. LifeTime and improving European healthcare through cell-based interceptive medicine

27. Dissecting the phenotypic heterogeneity in sensory features in autism spectrum disorder: a factor mixture modelling approach

34. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

36. Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

39. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

42. Identification of genetic interactions involved in dyslexia pathogenesis

43. Lack of replication of previous autism spectrum disorder GWAS hits in European populations

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

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

46. Lack of replication of previous autism spectrum disorder GWAS hits in European populations

48. Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition

49. Linkage and association of the glutamate receptor 6 gene with autism

50. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

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