47 results on '"Jacquemont, Sebastien"'
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2. Subcortical Brain Alterations Across Copy Number Variants Converge With Those in Severe Mental Illnesses
3. Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disorders
4. Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers
5. Exploring the common genetic architecture of autism spectrum disorder using a novel multi-polygenic risk score approach
6. 70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA
7. 37. PREDICTING COGNITIVE AND ADAPTIVE OUTCOMES IN INDIVIDUALS WITH AUTISM USING GENOMIC VARIANTS AND EARLY DEVELOPMENTAL MILESTONES.
8. T55. DESCRIBING THE BROAD SPECTRUM OF CNVS EFFECT SIZES ON COGNITIVE ABILITY ACROSS BRAIN AND NON-BRAIN TISSUE
9. F66. FROM GENE TO COGNITION: MAPPING THE EFFECTS OF GENOMIC DELETIONS AND DUPLICATIONS ON COGNITIVE ABILITY
10. 69. GENOME-WIDE ASSOCIATION OF COPY NUMBER VARIANTS ACROSS SIX MAJOR PSYCHIATRIC DISORDERS REVEALS GENOTYPE-PHENOTYPE RELATIONSHIPS OF RARE VARIANTS
11. 66. PREFERENTIAL EFFECTS ON COGNITIVE ABILITY OF DELETIONS VERSUS DUPLICATIONS ACROSS BIOLOGICAL FUNCTIONS.
12. Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank
13. W66. COPY NUMBER VARIANTS AND THE TANGENTIAL GROWTH OF THE CEREBRAL CORTEX
14. 453. Diffusion Tensor Imaging White Matter Abnormalities Associated With Copy Number Variants: A Normative Modeling Approach
15. Genesis, modelling and methodological remedies to autism heterogeneity
16. Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry
17. 34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS
18. Interactive Effects of Common and Rare Genetic Variants on Psychopathology in the UK Biobank
19. P414. Effect Sizes Map on General Intelligence of Coding Genes Deleted or Duplicated
20. P163. Fiber Density vs. Dispersion in 16p11.2 Deletion: A Multi-Site Study of Advanced Diffusion MRI Measures
21. Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank
22. Structural and functional brain alterations revealed by neuroimaging in CNV carriers
23. White Matter Diffusion MRI Findings in Carriers of 16p11.2 Copy Number Variants
24. The General Impact of Haploinsufficiency on Brain Connectivity Underlies the Pleiotropic Effect of Neuropsychiatric CNVS
25. ENIGMA-CNV and Other Initiatives to Understand the Impact of Rare Copy Number Variants on Brain Structure and Other Measures
26. Omnigenic Impact of Copy Number Variants on Cognition and Psychopathology in the Philadelphia Neurodevelopmental Cohort
27. Functional Connectivity Analyses Suggest Shared Molecular Mechanisms Across 12 Neuropsychiatric Mutations, Autism and Schizophrenia
28. Estimating the Effect Size of CNVs on Risk for Major Psychopathology, the CAMP Project
29. Measuring and Estimating the Effect Size of Rare Non-Recurrent Deletions and Duplications on General Intelligence
30. Insufficient Evidence for “Autism-Specific” Genes
31. 40 MAPPING THE EFFECT-SIZE OF GENE DOSAGE ON GENERAL INTELLIGENCE ACROSS THE GENOME
32. 5 DIFFERENCES IN THE GENETIC BACKGROUND CONTRIBUTE TO RISK AND RESILIENCE TO AUTISM
33. 251. Measuring and Estimating the Effects of Rare Variants, Genome-Wide, on Cognition
34. 250. Gene Dosage Effects on Neurobehavioral Phenotypes and Development: Relevance to Idiopathic Neuropsychiatric Disorders
35. 188. ENIGMA-CNV: Unraveling the Effects of Rare Copy Number Variants on Brain Structure
36. 191. Mirror Effects of 4 Neurodevelopmental CNVs on Functional Connectivity and Implication for Idiopathic Autism
37. Rare Copy-Number variations and neuropsychiatric development disorders
38. SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant
39. SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant
40. Transmission Disequilibrium of Small CNVs in Simplex Autism
41. Phenotypic and molecular characterization of a novel case of dyssegmental dysplasia, Silverman-Handmaker type
42. Preimplantation genetic diagnosis (PGD) for HLA typing: bases for setting up an open international collaboration when PGD is not available
43. Lifespan changes in working memory in fragile X premutation males
44. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
45. Age-dependent cognitive changes in carriers of the fragile X syndrome
46. Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1
47. Inherited ring chromosome 8 without loss of subtelomeric sequences
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