Publications of Bertram Müller-Myhsok
All genres
Journal Article (387)
2017
Journal Article
211 (2), pp. 70 - 76 (2017)
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. BRITISH JOURNAL OF PSYCHIATRY
Journal Article
16 (11), pp. 898 - 907 (2017)
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. LANCET NEUROLOGY
Journal Article
8, 1511 (2017)
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS
Journal Article
8 (7), 183 (2017)
Genetic Contribution to Alcohol Dependence: Investigation of Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. GENES
Journal Article
58 (9), pp. 998 - 1007 (2017)
Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
Journal Article
58 (9), pp. 1011 - 1013 (2017)
Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017). JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
Journal Article
7, e1155 (2017)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. TRANSLATIONAL PSYCHIATRY
Journal Article
7, 1273 (2017)
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. TRANSLATIONAL PSYCHIATRY
Journal Article
82 (5), pp. 312 - 321 (2017)
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. BIOLOGICAL PSYCHIATRY 2016
Journal Article
19 (12), pp. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE
Journal Article
53 (10), pp. 6608 - 6619 (2016)
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. MOLECULAR NEUROBIOLOGY
Journal Article
24 (10), pp. 1488 - 1495 (2016)
Genetic variants in RBFOX3 are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS
Journal Article
12 (10), e1006343 (2016)
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLOS GENETICS
Journal Article
76 (17), pp. 5103 - 5114 (2016)
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. CANCER RESEARCH
Journal Article
48 (8), pp. 856 - + (2016)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. NATURE GENETICS
Journal Article
2 (6), e1501678 (2016)
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. SCIENCE ADVANCES
Journal Article
36 (7), pp. 648 - 657 (2016)
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. SI
Journal Article
46 (2), pp. 151 - 169 (2016)
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. BEHAVIOR GENETICS
Journal Article
19 (12), pp. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE 2015
Journal Article
39 (8), pp. 601 - 608 (2015)
Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array. GENETIC EPIDEMIOLOGY