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 · 716 citations

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, Jenny M. Gunnersen et al. · Proceedings of the National Academy of Sciences · 1997 · 657 citations

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

B. D. Williams, Bertold Schrank, Chau Huynh et al. · Genetics · 1992 · 498 citations · Full text

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 · 304 citations

Late-onset Leigh Syndrome, Mitochondrial Function, Genetic Disorder +8

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 · 188 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Placebo-controlled Double-blind Study +7