J. Vogt

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

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

Angelika C. Roehl, J. Vogt, Antje N. Zickler et al. · Human Mutation · 2010 · 37 citations · Full text

Genetics, Genomic Mechanism, Molecular Genetics +20

Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutation

J. Vogt, Juergen Kohlhase · Human Mutation · 2011 · 36 citations · Full text

Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis

Julien Broséus, Sébastien Hergalant, J. Vogt et al. · Nature Communications · 2023 · 34 citations · Full text

Engineering, Genetics, Immunology +21