Publications Bertram Müller-Myhsok
Journal Article (17)
1.
Journal Article
8 (11), e79145 (2013)
Rare Variants in PLXNA4 and Parkinson's Disease. PLOS ONE 2.
Journal Article
45 (9), pp. 984 - 994 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. NATURE GENETICS 3.
Journal Article
43 (9), pp. 1965 - 1971 (2013)
Estimating the heritability of reporting stressful life events captured by common genetic variants. PSYCHOLOGICAL MEDICINE 4.
Journal Article
45 (8), pp. 912 - U255 (2013)
Genome-wide meta-analysis identifies new susceptibility loci for migraine. NATURE GENETICS 5.
Journal Article
23 (7), pp. 653 - 662 (2013)
Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. EUROPEAN NEUROPSYCHOPHARMACOLOGY 6.
Journal Article
8 (6), e64947 (2013)
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach. PLOS ONE 7.
Journal Article
54 (6), pp. 686 - 694 (2013)
Predictors of developmental dyslexia in European orthographies with varying complexity. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 8.
Journal Article
43 (6), pp. 1207 - 1217 (2013)
Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders. PSYCHOLOGICAL MEDICINE 9.
Journal Article
8 (5), e63859 (2013)
Children with ADHD Symptoms Have a Higher Risk for Reading, Spelling and Math Difficulties in the GINIplus and LISAplus Cohort Studies. PLOS ONE 10.
Journal Article
110 (20), pp. 8302 - 8307 (2013)
Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 11.
Journal Article
74 (3-4), pp. 129 - 141 (2013)
Using Affected Sib-Pairs to Uncover Rare Disease Variants. HUMAN HEREDITY 12.
Journal Article
21 (4), pp. 367 - 372 (2013)
Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. EUROPEAN JOURNAL OF HUMAN GENETICS 13.
Journal Article
45 (4), pp. 392 - 398 (2013)
Genome-wide association studies identify four ER negative-specific breast cancer risk loci. NATURE GENETICS 14.
Journal Article
21 (4), pp. 410 - 414 (2013)
Dilution of candidates: the case of iron-related genes in restless legs syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 15.
Journal Article
3, e229 (2013)
A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. TRANSLATIONAL PSYCHIATRY 16.
Journal Article
18 (1), pp. 122 - 132 (2013)
A K-ATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila. MOLECULAR PSYCHIATRY 17.
Journal Article
52 (1), pp. 91 - 95 (2013)
Cost-effective GPU-Grid for Genome-wide Epistasis Calculations. METHODS OF INFORMATION IN MEDICINE Meeting Abstract (1)
18.
Meeting Abstract
14(Suppl.1), P18. European Headache and Migraine Trust International Congress, London, UK, September 20, 2012 - September 23, 2012. (2013)
Migraine without aura: genome-wide association analysis identifies several novel susceptibility. In JOURNAL OF HEADACHE AND PAIN,