B. Vetter

Sex ratio in populations of Silene otites in relation to vegetation cover, population size and fungal infection

S. Klotz, L. Soldaat, B. Vetter, 1997 .

Phenylketonuria and hyperphenylalaninemia in eastern Germany: A characteristic molecular profile and 15 novel mutations

A. Kulozik, C. Wolf, J. Hennermann, 2000, Human mutation.

Hereditary Thrombophilia in Cerebral Venous Thrombosis

S. Ziemer, A. Kulozik, S. Castell, 2000, Cerebrovascular Diseases.

Association of Factor V Leiden Mutation with Delayed Graft Function, Acute Rejection Episodes and Long-term Graft Dysfunction in Kidney Transplant Recipients

T. Slowinski, A. Kulozik, H. Neumayer, 2002, Thrombosis and Haemostasis.

Increased rate of factor V Leiden mutation in patients with cerebral venous thrombosis

S. Ziemer, A. Kulozik, J. Valdueza, 1998, Journal of Neurology.

Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis.

A. Kulozik, J. Valdueza, S. Mehraein, 1998, Stroke.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening

S. Grünert, B. Vetter, E. Lausch, 2015, BMC Medical Genetics.