Doctoral thesis

THORSTEN MANFRED KRANZ (2012):
Potential candidate genes for neuropsychiatric disorders: MLC1, C15orf53 and OXTR

MICHELLE KAIQI LIN (2011):
Genetics of common psychiatric disorders: A Mendelian perspective based on genetic analyses of lage pedigrees

DARJA HENSELER (2010):
Untersuchung potentieller Kandidatengene für Periodische Katatonie und Schizophrenie:
Strukturelle und funktionelle Promoteranalyse von Mlc1, Mutationsanalyse von BUB1B und Assoziationsstudien zu CHRNA7, DAOA und BRD1

HAUKUR PALMASON (2009):
The effects of catechol-O-methyltransferase (COMT) and psychosocial risk factors on symptom severity and co-morbid Conduct Disorder in Attention-Deficit/Hyperactivity Disorder“
(J. Neural Transm. 117(2): 259-67, 2010).

MARION TEGETHOFF (2009):
„Fetal origins of pediatric disease: Fetoplacental plasticity and intrauterine programming by stress and glucocorticoids“ 

DIRK MOSER (2008):
„Linking genetic variation and epigenetic modification: Functional promoter analysis of SCL12A6 and NR3C1, two candidate genes involved in the pathogenesis of mood disorders“
(Neuropsychopharmacology 34: 458-467, 2009; World J. Biol. Psychiatr. 8: 262-268, 2007).

SAVIRA EKAWARDHANI (2008):
„Dissection of schizophrenia susceptibility loci at chromosomes 14q14-15.1 and 22q13.33“
(Schizophr. Res. 75: 1-3, 2005)