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Article

Familiality and molecular genetics of attention networks in ADHD.
Konrad, K., Dempfle, A., Friedel, S., Heiser, P., Holtkamp, K., Walitza, S., Sauer, S. ORCID logoORCID: https://orcid.org/0000-0002-4794-3693, 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

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