Publications of D. Czamara

Becker, J.; Czamara, D.; Hoffmann, P.; Landerl, K.; Blomert, L.; Brandeis, D.; Vaessen, A.; Maurer, U.; Moll, K.; Ludwig, K. U. et al.; Müller-Myhsok, B.; Nöthen, M. M.; Schulte-Körne, G.; Schumacher, J.: Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry 2, e136 (2012)

Menke, A.; Sämann, P.; Kloiber, S.; Czamara, D.; Lucae, S.; Hennings, J.; Heck, A.; Kohli, M. A.; Czisch, M.; Müller-Myhsok, B. et al.; Holsboer, F.; Binder, E. B.: Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology 37 (4), pp. 565 - 575 (2012)

Glas, J.; Seiderer, J.; Wagner, J.; Olszak, T.; Fries, C.; Tillack, C.; Friedrich, M.; Beigel, F.; Stallhofer, J.; Steib, C. et al.; Wetzke, M.; Göke, B.; Ochsenkühn, T.; Diegelmann, J.; Czamara, D.; Brand, S.: Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. PLoS ONE 7 (3), e34349 (2012)

Glas, J.; Wagner, J.; Seiderer, J.; Olszak, T.; Wetzke, M.; Beigel, F.; Tillack, C.; Stallhofer, J.; Friedrich, M.; Steib, C. et al.; Göke, B.; Ochsenkühn, T.; Karbalai, N.; Diegelmann, J.; Czamara, D.; Brand, S.: PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background. PLoS ONE 7 (3), e33682 (2012)

Menke, A.; Domschke, K.; Czamara, D.; Klengel, T.; Hennings, J.; Lucae, S.; Baune, B. T.; Arolt, V.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology 37 (3), pp. 797 - 807 (2012)

Glas, J.; Seiderer, J.; Bayrle, C.; Wetzke, M.; Fries, C.; Tillack, C.; Olszak, T.; Beigel, F.; Steib, C.; Friedrich, M. et al.; Diegelmann, J.; Czamara, D.; Brand, S.: The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease. PLoS ONE 6 (12), e29309 (2011)

Heck, A.; Pfister, H.; Czamara, D.; Müller-Myhsok, B.; Pütz, B.; Lucae, S.; Hennings, J.; Ising, M.: Evidence for associations between MDGA2 polymorphisms and harm avoidance - replication and extension of a genome-wide association finding. Psychiatric Genetics 21 (5), pp. 257 - 260 (2011)

Klengel, T.; Heck, A.; Pfister, H.; Brückl, T.; Hennings, J. M.; Menke, A.; Czamara, D.; Müller-Myhsok, B.; Ising, M.: Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica 124 (4), pp. 317 - 328 (2011)

Glas, J.; Seiderer, J.; Fischer, D.; Tengler, B.; Pfennig, S.; Wetzke, M.; Beigel, F.; Olszak, T.; Weidinger, M.; Göke, B. et al.; Ochsenkühn, T.; Folwaczny, M.; Müller-Myhsok, B.; Diegelmann, J.; Czamara, D.; Brand, S.: Pregnane X Receptor (PXR/NR1I2) Gene Haplotypes Modulate Susceptibility to Inflammatory Bowel Disease. Inflammatory Bowel Diseases 17 (9), pp. 1917 - 1924 (2011)

Hennings, J. M.; Kohli, M. A.; Czamara, D.; Wolf, C.; Domschke, K.; Arolt, V.; Baune, T.; Horstmann, S.; Brückl, T.; Klengel, T. et al.; Menke, A.; Müller-Myhsok, B.; Ising, M.; Uhr, M.; Lucae, S.: BDNF and NTRK2 polymorphisms and antidepressant treatment outcome. Pharmacopsychiatry 44 (6), p. 295 - 295 (2011)

Lucae, S.; Czamara, D.; Uhr, M.; Ising, M.; Holsboer, F.; Müller-Myhsok, B.: 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 44 (6), p. 300 - 300 (2011)

Schormair, B.; Plag, J.; Kaffe, M.; Gross, N.; Czamara, D.; Samtleben, W.; Lichtner, P.; Ströhle, A.; Stefanidis, I.; Vainas, A. et al.; Dardiotis, E.; Sakkas, G. K.; Gieger, C.; Müller-Myhsok, B.; Meitinger, T.; Heemann, U.; Hadjigeorgiou, G. M.; Oexle, K.; Winkelmann, J.: MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. Journal of Medical Genetics 48 (7), pp. 462 - 466 (2011)

Winkelmann, J.; Czamara, D.; Schormair, B.; Knauf, F.; Schulte, E. C.; Trenkwalder, C.; Dauvilliers, Y.; Polo, O.; Högl, B.; Berger, K. et al.; Fuhs, A.; Gross, N.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Xiong, L.; Montplaisir, J.; Rouleau, G. A.; Fietze, I.; Vavrova, J.; Kemlink, D.; Sonka, K.; Nevsimalova, S.; Lin, S. C.; Wszolek, Z.; Vilarino-Guell, C.; Farrer, M. J.; Gschliesser, V.; Frauscher, B.; Falkenstetter, T.; Poewe, W.; Allen, R. P.; Earley, C. J.; Ondo, W. G.; Le, W. D.; Spieler, D.; Kaffe, M.; Zimprich, A.; Kettunen, J.; Perola, M.; Silander, K.; Cournu-Rebeix, I.; Francavilla, M.; Fontenille, C.; Fontaine, B.; Vodicka, P.; Prokisch, H.; Lichtner, P.; Peppard, P.; Faraco, J.; Mignot, E.; Gieger, C.; Illig, T.; Wichmann, H. E.; Müller-Myhsok, B.; Meitinger, T.: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1. PLoS Genetics 7 (7), e1002171 (2011)

Glas, J.; Seiderer, J.; Tillack, C.; Paschos, E.; Wetzke, M.; Diegelmann, J.; Czamara, D.; Brand, S.: Functional SFTPD Gene Variants Are Not Associated with Susceptibility to Inflammatory Bowel Disease in the German Population. Inflammatory Bowel Diseases 17 (6), pp. 1439 - 1440 (2011)

Hennings, J. M.; Kohli, M. A.; Czamara, D.; Heck, A.; Domschke, K.; Arolt, V.; Baune, B.; Horstmann, S.; Brueckl, T.; Klengel, T. et al.; Menke, A.; Müller-Myhsok, B.; Ising, M.; Uhr, M.; Holsboer, F.; Lucae, S.: BDNF and NTRK2 Polymorphisms and Antidepressant Treatment Response. Biological Psychiatry 69 (9 Suppl.1), p. 152 S - 152 S (2011)

Glas, J.; Seiderer, J.; Fries, C.; Tillack, C.; Pfennig, S.; Weidinger, M.; Beigel, F.; Olszak, T.; Lass, U.; Göke, B. et al.; Ochsenkühn, T.; Wolf, C.; Lohse, P.; Müller-Myhsok, B.; Diegelmann, J.; Czamara, D.; Brand, S.: CEACAM6 Gene Variants in Inflammatory Bowel Disease. PLoS ONE 6 (4), e19319 (2011)

Kam-Thong, T.; Czamara, D.; Tsuda, K.; Borgwardt, K.; Lewis, C. M.; Erhardt-Lehmann, A.; Hemmer, B.; Rieckmann, P.; Daake, M.; Weber, F. et al.; Wolf, C.; Ziegler, A.; Pütz, B.; Holsboer, F.; Schölkopf, B.; Müller-Myhsok, B.: EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units. European Journal of Human Genetics 19 (4), pp. 465 - 471 (2011)

Czamara, D.; Bruder, J.; Becker, J.; Bartling, J.; Hoffmann, P.; Ludwig, K. U.; Müller-Myhsok, B.; Schulte-Körne, G.: Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia. Behavior Genetics 41 (1), pp. 110 - 119 (2011)

Glas, J.; Seiderer, J.; Tillack, C.; Pfennig, S.; Beigel, F.; Jürgens, M.; Olszak, T.; Laubender, R. P.; Weidinger, M.; Müller-Myhsok, B. et al.; Göke, B.; Ochsenkühn, T.; Lohse, P.; Diegelmann, J.; Czamara, D.; Brand, S.: The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. PLoS ONE 5 (12), e14466 (2010)

Czamara, D.; Mehta, D.: Statistical genetic concepts in psychiatric genomics. In: PERSONALIZED PSYCHIATRY, pp. 103 - 116. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD, 125 LONDON WALL, LONDON EC2Y 5AS, ENGLAND (2020)