Kathrin Bengesser

Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)

Ludwine M. Messiaen, J. Vogt, Kathrin Bengesser et al. · Human Mutation · 2010 · 115 citations · Full text

Neuro-oncology, Nf1 Deletions, Segmental Neurofibromatosis Type-1 +13

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

J. Vogt, Kathrin Bengesser, Kathleen Claes et al. · Genome biology · 2014 · 85 citations · Full text

A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Kathrin Bengesser, D.N. Cooper, Katharina Steinmann et al. · Human Mutation · 2010 · 40 citations · Full text

Internal tumor burden in neurofibromatosis Type I patients with large <i>NF1</i> deletions

Lan Kluwe, Rosa Nguyen, J. Vogt et al. · Genes Chromosomes and Cancer · 2012 · 33 citations

Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3<i>NF1</i>deletions

Antje M. Zickler, Stephanie Hampp, Ludwine Messiaen et al. · Human Mutation · 2011 · 30 citations