Publikationen von D. Czamara
Alle Typen
Zeitschriftenartikel (118)
2012
Zeitschriftenartikel
37 (4), S. 565 - 575 (2012)
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology
Zeitschriftenartikel
7 (3), e34349 (2012)
Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. PLoS ONE
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
Zeitschriftenartikel
37 (3), S. 797 - 807 (2012)
Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology 2011
Zeitschriftenartikel
6 (12), e29309 (2011)
The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease. PLoS ONE
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
Zeitschriftenartikel
124 (4), S. 317 - 328 (2011)
Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica
Zeitschriftenartikel
17 (9), S. 1917 - 1924 (2011)
Pregnane X Receptor (PXR/NR1I2) Gene Haplotypes Modulate Susceptibility to Inflammatory Bowel Disease. Inflammatory Bowel Diseases
Zeitschriftenartikel
44 (6), S. 295 - 295 (2011)
BDNF and NTRK2 polymorphisms and antidepressant treatment outcome. Pharmacopsychiatry
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
Zeitschriftenartikel
48 (7), S. 462 - 466 (2011)
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. Journal of Medical Genetics
Zeitschriftenartikel
7 (7), e1002171 (2011)
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1. PLoS Genetics
Zeitschriftenartikel
17 (6), S. 1439 - 1440 (2011)
Functional SFTPD Gene Variants Are Not Associated with Susceptibility to Inflammatory Bowel Disease in the German Population. Inflammatory Bowel Diseases
Zeitschriftenartikel
69 (9 Suppl.1), S. 152 S - 152 S (2011)
BDNF and NTRK2 Polymorphisms and Antidepressant Treatment Response. Biological Psychiatry
Zeitschriftenartikel
6 (4), e19319 (2011)
CEACAM6 Gene Variants in Inflammatory Bowel Disease. PLoS ONE
Zeitschriftenartikel
19 (4), S. 465 - 471 (2011)
EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units. European Journal of Human Genetics
Zeitschriftenartikel
41 (1), S. 110 - 119 (2011)
Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia. Behavior Genetics 2010
Zeitschriftenartikel
5 (12), e14466 (2010)
The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. PLoS ONE Buchkapitel (1)
2020
Buchkapitel
Statistical genetic concepts in psychiatric genomics. In: PERSONALIZED PSYCHIATRY, S. 103 - 116. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD, 125 LONDON WALL, LONDON EC2Y 5AS, ENGLAND (2020)
Konferenzbeitrag (13)
2018
Konferenzbeitrag
44 (Suppl. 1), 16.4, S. S26 - S27 (2018)
EFFECT OF GENOTYPE AND EARLY ADVERSITY ENVIRONMENT ON DNA METHYLATION. 6th Biennial Conference of the Schizophrenia-International-Research-Society (SIRS), Florence, ITALY, 04. April 2018 - 08. April 2018. SCHIZOPHRENIA BULLETIN