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1. Cerebral small vessel disease genomics and its implications across the lifespan

2. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

3. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

4. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

5. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

6. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

7. Age at first birth in women is genetically associated with increased risk of schizophrenia

8. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

9. Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

10. Novel genetic loci associated with hippocampal volume

11. Genetic variants in RBFOX3 are associated with sleep latency

12. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

13. Common genetic variants influence human subcortical brain structures

14. Genome-wide studies of verbal declarative memory in nondemented older people: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

15. MicroRNA related polymorphisms and breast cancer risk

16. The challenges of genome-wide interaction studies: Lessons to learn from the analysis of HDL blood levels

17. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

18. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

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