Stephanie Schneider

Adults with Philadelphia chromosome–like acute lymphoblastic leukemia frequently have <i>IGH-CRLF2</i> and <i>JAK2</i> mutations, persistence of minimal residual disease and poor prognosis

Tobias Herold, Stephanie Schneider, Klaus H. Metzeler et al. · Haematologica · 2016 · 164 citations · Full text

Life Sciences, Genetics, Hematology +17

GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia

Philipp A. Greif, Annika Dufour, Nikola P. Konstandin et al. · Blood · 2012 · 147 citations

Life Sciences, Genetics, Molecular Genetics +16

A 29-gene and cytogenetic score for the prediction of resistance to induction treatment in acute myeloid leukemia

Tobias Herold, Vindi Jurinović, Aarif M.N. Batcha et al. · Haematologica · 2017 · 140 citations · Full text

Medicine, Biostatistics, Oncology +17

Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis

Tobias Herold, Klaus H. Metzeler, Sebastian Vosberg et al. · Blood · 2014 · 105 citations

Life Sciences, Genetics, Molecular Genetics +15

An Advanced Preclinical Mouse Model for Acute Myeloid Leukemia Using Patients' Cells of Various Genetic Subgroups and In Vivo Bioluminescence Imaging

Binje Vick, Maja Rothenberg, Nadine Sandhöfer et al. · PLoS ONE · 2015 · 96 citations · Full text

Medicine, Cell Biology, Oncology +14