Friederike Schneider

Acute Myeloid Leukemia With Biallelic <i>CEBPA</i> Gene Mutations and Normal Karyotype Represents a Distinct Genetic Entity Associated With a Favorable Clinical Outcome

Annika Dufour, Friederike Schneider, Klaus H. Metzeler et al. · Journal of Clinical Oncology · 2009 · 292 citations · Full text

Expression of the embryonic stem cell marker SOX2 in early-stage breast carcinoma

Claudia Lengerke, Tanja Fehm, Ralf Kurth et al. · BMC Cancer · 2011 · 190 citations · Full text

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

RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes

Philipp A. Greif, Nikola P. Konstandin, Klaus H. Metzeler et al. · Haematologica · 2012 · 98 citations · Full text

Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML (NK-AML)

Friederike Schneider, Eva Hoster, Stephanie Schneider et al. · Annals of Hematology · 2011 · 80 citations

Age-dependent Frequencies, Genetic Disorder, Medicine +7