Winfried Hofmann

The identification of pathogenic variants in <i>BRCA1/2</i> negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of <i>FANCM</i> pathogenic variants

Stephanie Schubert, Jana Lisa van Luttikhuizen, Bernd Auber et al. · International Journal of Cancer · 2018 · 86 citations · Full text

Breast Oncology, Genetics, Genetic Epidemiology +16

Telomere shortening and chromosomal instability in myelodysplastic syndromes

Kathrin Lange, Lisa Holm, Kirsten Vang Nielsen et al. · Genes Chromosomes and Cancer · 2009 · 80 citations

Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair

Ilona Kalasová, Richard Hailstone, Janin Bublitz et al. · Nucleic Acids Research · 2020 · 45 citations · Full text

Dna Damage, Genetics, Molecular Biology +18

Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia

Maximilian Schieck, Jana Lentes, Kathrin Thomay et al. · Annals of Hematology · 2020 · 40 citations · Full text

A ‘telomere-associated secretory phenotype’ cooperates with BCR-ABL to drive malignant proliferation of leukemic cells

Melanie Braig, Nora Pällmann, Michael Preukschas et al. · Leukemia · 2014 · 36 citations

Hematological Malignancy, Cancer Research, Leukemic Cells +10