Beatrice Schuster

Mutation of the RAD51C gene in a Fanconi anemia–like disorder

Fiona Vaz, Helmut Hanenberg, Beatrice Schuster et al. · Nature Genetics · 2010 · 402 citations

Genetic Disorder, Genetics, Molecular Biology +4

Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker et al. · The American Journal of Human Genetics · 2013 · 303 citations · Full text

Genome Instability, Genetic Disorder, Genetics +6

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

Chantal Stoepker, Karolina Hain, Beatrice Schuster et al. · Nature Genetics · 2011 · 295 citations

Genetic Disorder, Natural Sciences, Genetics +9

A Histone-Fold Complex and FANCM Form a Conserved DNA-Remodeling Complex to Maintain Genome Stability

Zhijiang Yan, Mathieu Delannoy, Ling Chen et al. · Molecular Cell · 2010 · 230 citations · Full text

Chromatin, Fancm Form, Chromatin Structure +14

Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges

Kerstin Knies, Beatrice Schuster, Najim Ameziane et al. · PLoS ONE · 2012 · 39 citations · Full text

Bioinformatics, Fanconi Anemia, Long-read Sequencing +15