Bertold Schrank

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton et al. · Science · 1992 · 718 citations

Life Sciences, Genetics, Molecular Genetics +17

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

Bertold Schrank, Rudolf Götz, Janice Ure et al. · Proceedings of the National Academy of Sciences · 1997 · 658 citations

Life Sciences, Genetics, Molecular Genetics +17

A genetic mapping system in Caenorhabditis elegans based on polymorphic sequence-tagged sites.

B. D. Williams, Bertold Schrank, Chau Huynh et al. · Genetics · 1992 · 500 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome

Woranontee Weraarpachai, Hana Antonická, Florin Sasarman et al. · Nature Genetics · 2009 · 309 citations

Life Sciences, Genetics, Molecular Biology +5

High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study

Michael Graf, D. Ecker, R. Horowski et al. · Journal of Neural Transmission · 2004 · 191 citations

Life Sciences, Neurology, Neuroscience +13