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  1. No Access

    Article

    Further evidence for a modulation of Novelty Seeking by DRD4 exon III, 5-HTTLPR, and COMT val/met variants

    A Strobel, K P Lesch, S Jatzke, F Paetzold, B Brocke in Molecular Psychiatry (2003)

  2. No Access

    Article

    No association between dopamine D4 receptor gene exon III and –521C/T polymorphism and Novelty Seeking

    A Strobel, K P Lesch, K Hohenberger, S Jatzke, H O Gutzeit… in Molecular Psychiatry (2002)

  3. No Access

    Article

    A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree

    Schizophrenia is a common and etiologically heterogeneous disorder. Although inheritance of schizophrenic syndromes is complex with genetic and environmental factors contributing to the clinical phenotype, per...

    J Meyer, A Huberth, G Ortega, Y V Syagailo, S Jatzke, R Mössner… in Molecular Psychiatry (2001)

  4. No Access

    Article

    Mosaicism for a serotonin transporter gene promoter-associated deletion: decreased recombination in depression

    Transcriptional activity of the human serotonin transporter gene (5HTT) is modulated by complex interaction of multiple genomic and cellular factors. Variability of a polymorphic repetitive element (5HTTLPR) is ...

    K. P. Lesch, S. Jatzke, J. Meyer, G. Stöber, O. Okladnova… in Journal of Neural Transmission (1999)

  5. No Access

    Article

    Insertion/deletion variant (−141C Ins/Del) in the 5′ regulatory region of the dopamine D2 receptor gene: lack of association with schizophrenia and bipolar affective disorder

    A possible dysregulation of dopaminergic neurotransmission has been implicated in the aetiology of schizophrenic psychoses, in particular of paranoid-hallucinatory states, and of the manic episodes of bipolar...

    G. Stöber, S. Jatzke, A. Heils, G. Jungkunz, M. Knapp… in Journal of Neural Transmission (1998)