Benigna von Brederlow

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Hanno J. Bolz, Benigna von Brederlow, Alfredo Ramı́rez et al. · Nature Genetics · 2001 · 497 citations

Life Sciences, Genetics, Molecular Genetics +6

Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex

Benigna von Brederlow, Andreas Fregin, Simone Rost et al. · Thrombosis and Haemostasis · 2000 · 105 citations

Medicine, Genetics, Molecular Genetics +17

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

Benigna von Brederlow, Angelika F. Hahn, Wilma J. Koopman et al. · Human Molecular Genetics · 1995 · 85 citations

Life Sciences, Genetics, Molecular Genetics +16

Identification and in vitro expression of novelCDH23 mutations of patients with Usher syndrome type 1D

Benigna von Brederlow, Hanno J. Bolz, Andreas Janecke et al. · Human Mutation · 2002 · 45 citations

Life Sciences, Genetics, Molecular Genetics +10

Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family

Hanno J. Bolz, Alfredo Ramı́rez, Benigna von Brederlow et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 2001 · 31 citations

Life Sciences, Biochemistry, Molecular Biology +7