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Familiality and molecular genetics of attention networks in ADHD.
Konrad, K., Dempfle, A., Friedel, S., Heiser, P., Holtkamp, K., Walitza, S., Sauer, S., Warnke, A., Remschmidt, H., Gilsbach, S., Schäfer, H., Hinney, A., Hebebrand, J. and Herpertz-Dahlmann, B.
American Journal of Medical Genetics B 153B (1): 148-158. 5 January 2010

Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus-Merzbacher-like leukodystrophy.
Ruf, N., Martelli, M., Weschke, B. and Uhlenberg, B.
American Journal of Medical Genetics B 144 (3): 365-366. 5 April 2007

Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.
Lorenz, S., Heils, A., Kasper, J.M. and Sander, T.
American Journal of Medical Genetics B 144B (1): 10-13. 5 January 2007

Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder.
Lohoff, F.W., Sander, T., Ferraro, T.N., Dahl, J.P., Gallinat, J. and Berrettini, W.H.
American Journal of Medical Genetics B 139 (1): 51-53. 5 November 2005

Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.
Izzi, C., Barbon, A., Toliat, M.R., Heils, A., Becker, C., Nuernberg, P., Sander, T. and Barlati, S.
American Journal of Medical Genetics B 123B (1): 59-63. 15 November 2003