Publikationen von Darina Czamara
Alle Typen
Zeitschriftenartikel (121)
2016
Zeitschriftenartikel
7, 10023 (2016)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. NATURE COMMUNICATIONS 2015
Zeitschriftenartikel
4 (11), S. 1700 - 1704 (2015)
Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma. CANCER MEDICINE
Zeitschriftenartikel
86 (5), S. 1189 - 1202 (2015)
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. NEURON
Zeitschriftenartikel
168 (4), S. 274 - 283 (2015)
ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Zeitschriftenartikel
10 (5), UNSP e0128465 (2015)
Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice. PLOS ONE
Zeitschriftenartikel
13, 86 (2015)
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. BMC MEDICINE
Zeitschriftenartikel
5, e538 (2015)
RNA expression profiling in depressed patients suggests retinoid-related orphan receptor alpha as a biomarker for antidepressant response. Translational psychiatry
Zeitschriftenartikel
279, S. 46 - 49 (2015)
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. JOURNAL OF NEUROIMMUNOLOGY
Zeitschriftenartikel
18 (2), S. 199 - 209 (2015)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. NATURE NEUROSCIENCE 2014
Zeitschriftenartikel
22 (5), S. 675 - 680 (2014)
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS
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
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 2013
Zeitschriftenartikel
8 (11), e79145 (2013)
Rare Variants in PLXNA4 and Parkinson's Disease. PLOS ONE
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
Zeitschriftenartikel
45 (9), S. 984 - 994 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. NATURE GENETICS
Zeitschriftenartikel
8 (6), e64947 (2013)
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach. PLOS ONE
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
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
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
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