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23 results on '"Joober, R."'

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1. Dopamine-system genes, childhood abuse, and clinical manifestations in women with Bulimia-Spectrum Disorders.

2. Interaction of the BcII glucocorticoid receptor polymorphism and childhood abuse in Bulimia Nervosa (BN): relationship to BN and to associated trait manifestations.

3. Contributions of the glucocorticoid receptor polymorphism (Bcl1) and childhood abuse to risk of bulimia nervosa.

4. The brain-derived neurotrophic factor Val66Met polymorphism is associated with reduced functional magnetic resonance imaging activity in the hippocampus and increased use of caudate nucleus-dependent strategies in a human virtual navigation task.

5. Association of trait-defined, eating-disorder sub-phenotypes with (biallelic and triallelic) 5HTTLPR variations.

6. Development and persistence of posttraumatic stress disorder and the 5-HTTLPR polymorphism.

7. COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.

8. Serotonin-system polymorphisms (5-HTTLPR and -1438G/A) and responses of patients with bulimic syndromes to multimodal treatments.

9. Relevance of the 5-HTTLPR polymorphism and childhood abuse to increased psychiatric comorbidity in women with bulimia-spectrum disorders.

10. Acute and long-term associations between ApoE genetic polymorphism, cortisol levels, and declarative memory performance in older adults.

11. Dissocial behavior, the 5HTTLPR polymorphism, and maltreatment in women with bulimic syndromes.

12. No association between the DRD3 Ser9Gly polymorphism and schizophrenia.

13. Sleep and COMT polymorphism in ADHD children: preliminary actigraphic data.

14. Association of the promoter polymorphism -1438G/A of the 5-HT2A receptor gene with behavioral impulsiveness and serotonin function in women with bulimia nervosa.

15. CAA insertion polymorphism in the 3'UTR of Nogo gene on 2p14 is not associated with schizophrenia.

16. The 5HTTLPR polymorphism, psychopathologic symptoms, and platelet [3H-] paroxetine binding in bulimic syndromes.

17. Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD.

18. Dopamine beta-hydroxylase (DBH) gene and schizophrenia phenotypic variability: a genetic association study.

19. Catechol-O-methyltransferase Val-108/158-Met gene variants associated with performance on the Wisconsin Card Sorting Test.

21. Evidence for a role of phospholipase C-gamma1 in the pathogenesis of bipolar disorder.

22. T102C polymorphism in the 5HT2A gene and schizophrenia: relation to phenotype and drug response variability

23. Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder

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