185 results on '"Bettecken, T."'
Search Results
2. Next Generation Sequencing in der diagnostischen Praxis: Von der Variante zum Befund
3. TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
4. Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways
5. The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders
6. IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations
7. Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
8. Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders
9. Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients
10. More CLEC16A gene variants associated with multiple sclerosis
11. Pharmacogenetics of antidepressant treatment outcome – Results from a genome-wide multilocus analysis including clinical predictors
12. Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism
13. A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy
14. Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation
15. Reduced amplification efficiency of KIAA0027/MLC1 alleles: implications for the molecular diagnosis of megalencephalic leukoencephalopathy with subcortical cysts
16. Genetik der Muskeldystrophien
17. MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene
18. The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects: Results in ~25,000 subjects
19. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
20. Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis
21. Multiplexing of primer extension products for mass spectrometry
22. Identification of risk loci with shared effects on five major psychiatric disorders:a genome-wide analysis
23. A mega-analysis of genome-wide association studies for major depressive disorder
24. Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges
25. More CLEC16A gene variants associated with multiple sclerosis
26. Segregation einer 220-kb-Insertion in die Bande Xp21.1 in einer Familie mit Duchennescher Muskeldystrophie
27. Systematic mutation analysis of KIAA0767 and KIAA I646 in chromosome 22q-linked periodic catatonia
28. Linkage analysis in myopia
29. Campomelic dysplasia without sex reversal in a Turkish patient is due to mutation Ala119Val within the SOX9 gene
30. Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders
31. Searching for biomarkers in a historic sample of Amyotrophic Lateral Sclerosis – The Munich Historic Brain Bank Project
32. A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy
33. More CLEC16A gene variants associated with multiple sclerosis
34. TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
35. A genome-wide association study points to multiple loci predicting antidepressant treatment outcome in depression
36. The Munich PTSD Biomarker Study (MPBS)
37. The neuronal transporter gene SLC6A15 confers risk to major depression
38. Characterisation of DNA methylation marks in stress exposed hippocampal astrocytes
39. Polymorphisms within the 4-aminobutyrate aminotransferase gene are associated with long-latency somatosensory potentials in families vulnerable for affective disorders
40. Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways
41. Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
42. The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders
43. No Association of Sequence Variants in the Neuropeptide Y2 Receptor (NPY2R) Gene with Early Onset Obesity in Germans
44. A genome-wide association study in patients with panic and anxiety disorders
45. Susceptibility gene hunting for recurrent unipolar depression using 400k genome-wide genotype data
46. Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients
47. Polymorphisms in the Leptin Gene are Associated with Resistance to Antidepressant Treatment and Lower Cognitive Performance in Depression
48. Whole genome analysis reveals new potential drug targets as predictors of antidepressant treatment response
49. Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
50. Sequence fossils, triplet expansion, and reconstruction of earliest codons
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