Publikationen von Bertram Müller-Myhsok
Alle Typen
Zeitschriftenartikel (387)
121.
Zeitschriftenartikel
211 (2), S. 70 - 76 (2017)
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. BRITISH JOURNAL OF PSYCHIATRY 122.
Zeitschriftenartikel
16 (11), S. 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 123.
Zeitschriftenartikel
8, 1511 (2017)
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS 124.
Zeitschriftenartikel
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 125.
Zeitschriftenartikel
58 (9), S. 998 - 1007 (2017)
Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 126.
Zeitschriftenartikel
58 (9), S. 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 127.
Zeitschriftenartikel
7, e1155 (2017)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. TRANSLATIONAL PSYCHIATRY 128.
Zeitschriftenartikel
7, 1273 (2017)
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. TRANSLATIONAL PSYCHIATRY 129.
Zeitschriftenartikel
82 (5), S. 312 - 321 (2017)
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. BIOLOGICAL PSYCHIATRY 130.
Zeitschriftenartikel
19 (12), S. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE 131.
Zeitschriftenartikel
53 (10), S. 6608 - 6619 (2016)
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. MOLECULAR NEUROBIOLOGY 132.
Zeitschriftenartikel
24 (10), S. 1488 - 1495 (2016)
Genetic variants in RBFOX3 are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS 133.
Zeitschriftenartikel
12 (10), e1006343 (2016)
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLOS GENETICS 134.
Zeitschriftenartikel
76 (17), S. 5103 - 5114 (2016)
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. CANCER RESEARCH 135.
Zeitschriftenartikel
48 (8), S. 856 - + (2016)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. NATURE GENETICS 136.
Zeitschriftenartikel
2 (6), e1501678 (2016)
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. SCIENCE ADVANCES 137.
Zeitschriftenartikel
36 (7), S. 648 - 657 (2016)
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. SI 138.
Zeitschriftenartikel
46 (2), S. 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 139.
Zeitschriftenartikel
19 (12), S. 1569 - 1582 (2016)
Novel genetic loci underlying human intracranial volume identified through genome-wide association. NATURE NEUROSCIENCE 140.
Zeitschriftenartikel
39 (8), S. 601 - 608 (2015)
Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array. GENETIC EPIDEMIOLOGY