S. Krey

Genetic heterogeneity of severe von Willebrand disease type III in the German population

Reinhard Schneppenheim, S. Krey, Frauke Bergmann et al. · Human Genetics · 1994 · 96 citations

German Population, Mendelian Disorder, Disease Etiology +13

Autosomal dominant ‘sector’ retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin

Holger Kranich, Sigrid Bartkowski, Michael J. Denton et al. · Human Molecular Genetics · 1993 · 86 citations

Ocular Disease, Genetics, Genetic Epidemiology +24

Results of a Screening for von Willebrand Disease Type 2N in Patients with Suspected Haemophilia A or von Willebrand Disease Type 1

Reinhard Schneppenheim, Ulrich Budde, S. Krey et al. · Thrombosis and Haemostasis · 1996 · 85 citations

Prevalence of factor V Leiden in children with thrombo-embolism

I. Aschka, V. Aumann, Frauke Bergmann et al. · European Journal of Pediatrics · 1996 · 84 citations

Pulmonary Embolism, Thrombosis, Venous Thrombosis +9

Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.

Reinhard Schneppenheim, Jacqueline Brassard, S. Krey et al. · Proceedings of the National Academy of Sciences · 1996 · 82 citations