Publikationen von D. Czamara
Alle Typen
Zeitschriftenartikel (131)
101.
Zeitschriftenartikel
19 (4), S. 452 - 461 (2014)
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. MOLECULAR PSYCHIATRY 102.
Zeitschriftenartikel
24 (4), S. 592 - 603 (2014)
Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon. GENOME RESEARCH 103.
Zeitschriftenartikel
8 (11), e79145 (2013)
Rare Variants in PLXNA4 and Parkinson's Disease. PLOS ONE 104.
Zeitschriftenartikel
8 (11), e77773 (2013)
Intestinal DMBT1 Expression Is Modulated by Crohn's Disease- Associated IL23R Variants and by a DMBT1 Variant Which Influences Binding of the Transcription Factors CREB1 and ATF-2. PLOS ONE 105.
Zeitschriftenartikel
45 (9), S. 984 - 994 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. NATURE GENETICS 106.
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8 (6), e64947 (2013)
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach. PLOS ONE 107.
Zeitschriftenartikel
43 (6), S. 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 108.
Zeitschriftenartikel
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 109.
Zeitschriftenartikel
21 (4), S. 410 - 414 (2013)
Dilution of candidates: the case of iron-related genes in restless legs syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 110.
Zeitschriftenartikel
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 111.
Zeitschriftenartikel
45 (2), S. 145 - 154 (2013)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics 112.
Zeitschriftenartikel
8 (1), e54338 (2013)
IRGM Variants and Susceptibility to Inflammatory Bowel Disease in the German Population. PLoS ONE 113.
Zeitschriftenartikel
2, e136 (2012)
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry 114.
Zeitschriftenartikel
37 (4), S. 565 - 575 (2012)
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology 115.
Zeitschriftenartikel
7 (3), e34349 (2012)
Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. PLoS ONE 116.
Zeitschriftenartikel
7 (3), e33682 (2012)
PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background. PLoS ONE 117.
Zeitschriftenartikel
37 (3), S. 797 - 807 (2012)
Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology 118.
Zeitschriftenartikel
6 (12), e29309 (2011)
The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease. PLoS ONE 119.
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 120.
Zeitschriftenartikel
124 (4), S. 317 - 328 (2011)
Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica