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Oncotarget|September 4, 2016
On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancerJudith Penkert, Tim Ripperger, Maximilian Schieck, et al.
European Journal of Medical Genetics|January 9, 2016
Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndromeTim Ripperger, Brigitte Schlegelberger
European Journal of Human Genetics : EJHG|December 19, 2008
Breast cancer susceptibility: current knowledge and implications for genetic counsellingTim Ripperger, Dorothea Gadzicki, Alfons Meindl, et al.
European Journal of Medical Genetics|March 5, 2018
12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literatureFrederik Heldt, Hannah Wallaschek, Tim Ripperger, et al.
Cancers|July 27, 2022
Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic MalignanciesAlisa Förster, Melanie Decker, Brigitte Schlegelberger, et al.
Biotechniques|October 11, 2012
Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGHGeorgi Manukjan, Marcel Tauscher, Tim Ripperger, et al.
Genes & Cancer|April 25, 2017
GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer familiesStephanie Schubert, Tim Ripperger, Melanie Rood, et al.
Stem Cell Research|April 22, 2016
GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemiaGeorgi Manukjan, Tim Ripperger, Letizia Venturini, et al.
Experimental Hematology|June 15, 2015
Expression of the ETS transcription factor GABPα is positively correlated to the BCR-ABL1/ABL1 ratio in CML patients and affects imatinib sensitivity in vitroGeorgi Manukjan, Tim Ripperger, Laura Santer, et al.
Breast Cancer Research : BCR|August 9, 2018
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredityJudith Penkert, Gunnar Schmidt, Winfried Hofmann, et al.
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