38 results on '"Franke, B"'
Search Results
2. ADHD-associated dopamine transporter, latrophilin and neurofibromin share a dopamine-related locomotor signature in Drosophila
3. Influence of DAT1 and COMT variants on neural activation during response inhibition in adolescents with attention-deficit/hyperactivity disorder and healthy controls
4. Influence of DAT1 and COMT variants on neural activation during response inhibition in adolescents with attention-deficit/hyperactivity disorder and healthy controls
5. A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides
6. A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschlʼs gyrus
7. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility
8. Attention deficit hyperactivity disorder (ADHD) and executive functioning in affected and unaffected adolescents and their parents: challenging the endophenotype construct
9. Cognitive flexibility depends on white matter microstructure of the basal ganglia
10. Common variant at 16p11.2 conferring risk of psychosis
11. Schizophrenia risk gene ZNF804A does not influence macroscopic brain structure: an MRI study in 892 volunteers
12. The genetics of attention deficit/hyperactivity disorder in adults, a review
13. BDNF Val66Met genotype modulates the effect of childhood adversity on subgenual anterior cingulate cortex volume in healthy subjects
14. Cost-of-illness analysis of Candidemia in patients on the intensive care unit: P734
15. Development of treatment costs of patients undergoing remission induction chemotherapy: A historical comparison before and after introduction of posaconazole prophylaxis: P044
16. Aetiology of hypospadias: a systematic review of genes and environment
17. Amygdala to hippocampal volume ratio is associated with negative memory bias in healthy subjects
18. CDH13 is associated with working memory performance in attention deficit/hyperactivity disorder
19. Depressive symptom clusters are differentially associated with atherosclerotic disease
20. A theoretical molecular network for dyslexia: integrating available genetic findings
21. Copy number variations of chromosome 16p13.1 region associated with schizophrenia
22. Interaction between dopamine D2 receptor genotype and parental rule-setting in adolescent alcohol use: evidence for a gene-parenting interaction
23. An international multicenter association study of the serotonin transporter gene in persistent ADHD
24. Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity
25. Parsing the role of dopamine in human reward and its cognitive consequences using genetic imaging
26. ASSOCIATION OF LOW-AFFINITY FC GAMMA RECEPTOR 3B (FCGR3B) COPY NUMBER VARIATION WITH RHEUMATOID ARTHRITIS IN CAUCASIAN SUBJECTS: C12
27. Gene expression profiling in rheumatoid arthritis: current concepts and future directions
28. The tumour necrosis factor receptor superfamily member 1b 676T>G polymorphism in relation to response to infliximab and adalimumab treatment and disease severity in rheumatoid arthritis
29. Familiality of major depressive disorder and gender differences in comorbidity
30. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16
31. Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: familial evidence for a distinct disorder
32. Motor coordination problems in children and adolescents with ADHD rated by parents and teachers: effects of age and gender
33. Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth
34. The association between HTR2C polymorphisms and obesity in psychiatric patients using antipsychotics: a cross-sectional study
35. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes
36. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
37. Genetic variation analysis of MLP, TFAP2A, and CSK in patients with neural tube defects
38. A case of euglycaemic diabetic ketoacidosis in pregnancy
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