Authors: Meyer, J Huberth, A Ortega, G Syagailo, YV Jatzke, S Mossner, R Strom, TM Ulzheimer-Teuber, I Stober, G Schmitt, A Lesch, KP

Citation: J. Meyer et al., A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree, MOL PSYCHI, 6(3), 2001, pp. 302-306

Authors: Stober, G Meyer, J Nanda, I Wienker, TF Saar, K Jatzke, S Schmid, M Lesch, KP Beckmann, H

Citation: G. Stober et al., hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodiccatatonia, a familial subtype of schizophrenia, EUR ARCH PS, 250(4), 2000, pp. 163-168

Authors: Stober, G Meyer, J Nanda, I Wienker, TF Saar, K Knapp, M Jatzke, S Schmid, M Lesch, KP Beckmann, H

Citation: G. Stober et al., Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13, AM J MED G, 96(3), 2000, pp. 392-397

Authors: Stober, G Saar, K Ruschendorf, F Meyer, J Nurnberg, G Jatzke, S Franzek, E Reis, A Lesch, KP Wienker, TF Beckmann, H

Citation: G. Stober et al., Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15, AM J HU GEN, 67(5), 2000, pp. 1201-1207

Authors: Lesch, KP Jatzke, S Meyer, J Stober, G Okladnova, O Mossner, R Riederer, P

Citation: Kp. Lesch et al., Mosaicism for a serotonin transporter gene promoter-associated deletion: decreased recombination in depression, J NEURAL TR, 106(11-12), 1999, pp. 1223-1230

Authors: Stober, G Jatzke, S Meyer, J Okladnova, O Knapp, N Beckmann, H Lesch, KP

Citation: G. Stober et al., Short CAG repeats within the hSKCa3 gene associated with schizophrenia: results of a family-based study, NEUROREPORT, 9(16), 1998, pp. 3595-3599