Andreas Ziegler

Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3.

A. Ziegler, K. Grzeschik, W. Lisch, 2000, American journal of ophthalmology.

Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents

K. Grzeschik, J. Hebebrand, A. Hinney, 2000, Acta Diabetologica.

Serum leptin levels increase rapidly after initiation of clozapine therapy

J. Hebebrand, H. Remschmidt, W. Blum, 1998, Molecular Psychiatry.

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population

A. Ziegler, M. Koch, K. Stegmann, 1998, European Journal of Pediatrics.

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).

A. Ziegler, M. Koch, N. Kohlschmidt, 1999, American journal of medical genetics.