266 results on '"Van Den Bree, Marianne B. M."'
Search Results
2. Author Correction: Using rare genetic mutations to revisit structural brain asymmetry
3. Using rare genetic mutations to revisit structural brain asymmetry
4. Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders
5. In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome
6. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
7. Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
8. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions
9. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
10. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study
11. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome
12. Detecting microstructural deviations in individuals with deep diffusion MRI tractometry
13. Effects of eight neuropsychiatric copy number variants on human brain structure
14. Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study
15. The psychiatric phenotypes of 1q21 distal deletion and duplication
16. Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication
17. Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders
18. Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology
19. Using rare genetic mutations to revisit structural brain asymmetry
20. Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk
21. Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD
22. Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication
23. DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts
24. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
25. Psychopathology in mothers of children with pathogenic Copy Number Variants.
26. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions
27. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome
28. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study
29. The Moderating Effects of Pubertal Timing on the Longitudinal Associations between Parent-Child Relationship Quality and Adolescent Substance Use
30. Examining Differences in Psychological Adjustment Problems among Children Conceived by Assisted Reproductive Technologies
31. Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study
32. The Developmental Relationship Between Depressive Symptoms in Adolescence and Harmful Drinking in Emerging Adulthood: The Role of Peers and Parents
33. Psychopathology in adults with copy number variants
34. Association of the CHRNA5-A3-B4 Gene Cluster With Heaviness of Smoking : A Meta-Analysis
35. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities
36. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome
37. Psychopathology among young homeless people: Longitudinal mental health outcomes for different subgroups
38. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
39. Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms.
40. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome
41. Mental health problems in young people with experiences of homelessness and the relationship with health service use: a follow-up study
42. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children
43. Sexual orientation and alcohol problem use among UK adolescents: an indirect link through depressed mood
44. Psychopathology and cognition in children with 22q11.2 deletion syndrome
45. Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder
46. Parent–Child Relations, Conduct Problems and Cigarette Use in Adolescence: Examining the Role of Genetic and Environmental Factors on Patterns of Behavior
47. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort
48. Combining research approaches to advance our understanding of drug addiction
49. Psychopathology in Young People Experiencing Homelessness: A Systematic Review
50. A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use
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