Publikationen von B. Müller-Myhsok
Alle Typen
Zeitschriftenartikel (387)
201.
Zeitschriftenartikel
44 (7), S. 777 - 782 (2012)
Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nature Genetics 202.
Zeitschriftenartikel
7 (5), e34909 (2012)
Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia. PLoS ONE 203.
Zeitschriftenartikel
37 (6), S. 1455 - 1464 (2012)
Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients. Neuropsychopharmacology 204.
Zeitschriftenartikel
159B (3), S. 263 - 273 (2012)
Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 205.
Zeitschriftenartikel
37 (4), S. 565 - 575 (2012)
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology 206.
Zeitschriftenartikel
20 (3), S. 321 - 325 (2012)
Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis. European Journal of Human Genetics 207.
Zeitschriftenartikel
44 (3), S. 328 - 333 (2012)
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nature Genetics 208.
Zeitschriftenartikel
44 (3), S. 312 - 318 (2012)
Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nature Genetics 209.
Zeitschriftenartikel
37 (3), S. 797 - 807 (2012)
Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology 210.
Zeitschriftenartikel
20 (2), S. 224 - 229 (2012)
Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics 211.
Zeitschriftenartikel
73 (4), S. 220 - 236 (2012)
GLIDE: GPU-Based Linear Regression for Detection of Epistasis. Human Heredity 212.
Zeitschriftenartikel
585 (23), S. 3789 - 3797 (2011)
Risk conferring genes in multiple sclerosis. FEBS Letters 213.
Zeitschriftenartikel
12 (Suppl. 11), A3 (2011)
Efficient branch-and-bound techniques for two-locus association mapping. BMC Bioinformatics 214.
Zeitschriftenartikel
21 (5), S. 257 - 260 (2011)
Evidence for associations between MDGA2 polymorphisms and harm avoidance - replication and extension of a genome-wide association finding. Psychiatric Genetics 215.
Zeitschriftenartikel
124 (4), S. 317 - 328 (2011)
Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica 216.
Zeitschriftenartikel
43 (10), S. 977 - 983 (2011)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nature Genetics 217.
Zeitschriftenartikel
17 (9), S. 1917 - 1924 (2011)
Pregnane X Receptor (PXR/NR1I2) Gene Haplotypes Modulate Susceptibility to Inflammatory Bowel Disease. Inflammatory Bowel Diseases 218.
Zeitschriftenartikel
44 (6), S. 295 - 295 (2011)
BDNF and NTRK2 polymorphisms and antidepressant treatment outcome. Pharmacopsychiatry 219.
Zeitschriftenartikel
44 (6), S. 300 - 300 (2011)
The non-synonymous P2RX7 SNP rs2230912 is associated with affective disorders: Results from an association study in major depression and from a meta-analysis. Pharmacopsychiatry 220.
Zeitschriftenartikel
68 (9), S. 901 - 910 (2011)
Using Polymorphisms in FKBP5 to Define Biologically Distinct Subtypes of Posttraumatic Stress Disorder Evidence From Endocrine and Gene Expression Studies. Archives of General Psychiatry