Publikationen von Darina Czamara
Alle Typen
Zeitschriftenartikel (129)
101.
Zeitschriftenartikel
8 (11), e79145 (2013)
Rare Variants in PLXNA4 and Parkinson's Disease. PLOS ONE 102.
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 103.
Zeitschriftenartikel
45 (9), S. 984 - 994 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. NATURE GENETICS 104.
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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 105.
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 106.
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 107.
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 108.
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 109.
Zeitschriftenartikel
45 (2), S. 145 - 154 (2013)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics 110.
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8 (1), e54338 (2013)
IRGM Variants and Susceptibility to Inflammatory Bowel Disease in the German Population. PLoS ONE 111.
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2, e136 (2012)
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry 112.
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37 (4), S. 565 - 575 (2012)
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology 113.
Zeitschriftenartikel
7 (3), e34349 (2012)
Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. PLoS ONE 114.
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 115.
Zeitschriftenartikel
37 (3), S. 797 - 807 (2012)
Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology 116.
Zeitschriftenartikel
6 (12), e29309 (2011)
The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease. PLoS ONE 117.
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 118.
Zeitschriftenartikel
124 (4), S. 317 - 328 (2011)
Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica 119.
Zeitschriftenartikel
17 (9), S. 1917 - 1924 (2011)
Pregnane X Receptor (PXR/NR1I2) Gene Haplotypes Modulate Susceptibility to Inflammatory Bowel Disease. Inflammatory Bowel Diseases 120.
Zeitschriftenartikel
44 (6), S. 295 - 295 (2011)
BDNF and NTRK2 polymorphisms and antidepressant treatment outcome. Pharmacopsychiatry