| Breast cancer susceptibility: current knowledge and implications for genetic counselling T Ripperger, D Gadzicki, A Meindl, B Schlegelberger European Journal of Human Genetics 17 (6), 722-731, 2009 | 309 | 2009 |
| Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology T Ripperger, SS Bielack, A Borkhardt, IB Brecht, B Burkhardt, ... American journal of medical genetics Part A 173 (4), 1017-1037, 2017 | 251 | 2017 |
| Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms B Tesi, J Davidsson, M Voss, E Rahikkala, TD Holmes, SCC Chiang, ... Blood 129 (16), 2266-2279, 2017 | 171 | 2017 |
| Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome T Ripperger, B Schlegelberger European journal of medical genetics 59 (3), 133-142, 2016 | 76 | 2016 |
| The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants A Rio-Machin, T Vulliamy, N Hug, A Walne, K Tawana, S Cardoso, ... Nature communications 11 (1), 1-12, 2020 | 69 | 2020 |
| Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants V Pastor, S Hirabayashi, A Karow, J Wehrle, EJ Kozyra, R Nienhold, ... Leukemia 31 (3), 759-762, 2017 | 67 | 2017 |
| Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519 C Rudolph, D Steinemann, N Von Neuhoff, D Gadzicki, T Ripperger, ... Cancer genetics and cytogenetics 153 (2), 144-150, 2004 | 67 | 2004 |
| Constitutional mismatch repair deficiency and childhood leukemia/lymphoma–report on a novel biallelic MSH6 mutation T Ripperger, C Beger, N Rahner, KW Sykora, CL Bockmeyer, U Lehmann, ... Haematologica 95 (5), 841, 2010 | 62 | 2010 |
| A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency K Wimmer, A Beilken, R Nustede, T Ripperger, B Lamottke, B Ure, ... Familial cancer 16 (1), 67-71, 2017 | 56 | 2017 |
| On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancer J Penkert, T Ripperger, M Schieck, B Schlegelberger, D Steinemann, ... Oncotarget 7 (41), 67626, 2016 | 51 | 2016 |
| Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy M Suerink, T Ripperger, L Messiaen, FH Menko, F Bourdeaut, C Colas, ... Journal of medical genetics 56 (2), 53-62, 2019 | 45 | 2019 |
| A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation? T Ripperger, D Steinemann, G Gohring, J Finke, CM Niemeyer, B Strahm, ... Leukemia 23 (7), 1364-1367, 2009 | 45 | 2009 |
| MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies T Ripperger, W Hofmann, JC Koch, K Shirneshan, D Haase, G Wulf, ... haematologica 103 (2), e55-e58, 2018 | 40 | 2018 |
| Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas. T Ripperger, N Neuhoff, K Kamphues, M Emura, U Lehmann, M Tauscher, ... | 37 | 2007 |
| The genetic message of a sudden, unexpected death due to thoracic aortic dissection T Ripperger, HD Tröger, J Schmidtke Forensic science international 187 (1), 1-5, 2009 | 35 | 2009 |
| A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes R Gallon, B Mühlegger, SS Wenzel, H Sheth, C Hayes, S Aretz, K Dahan, ... Human mutation 40 (5), 649-655, 2019 | 28 | 2019 |
| Constitutional trisomy 8p11. 21‐q11. 21 mosaicism: a germline alteration predisposing to myeloid leukaemia T Ripperger, M Tauscher, I Praulich, B Pabst, A Teigler‐Schlegel, A Yeoh, ... British journal of haematology 155 (2), 209-217, 2011 | 28 | 2011 |
| The RUNX1 Database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy CC Homan, SL King-Smith, DM Lawrence, P Arts, J Feng, J Andrews, ... Haematologica, 2020 | 25 | 2020 |
| A child with Li–Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies B Schlegelberger, H Kreipe, U Lehmann, D Steinemann, T Ripperger, ... Pediatric blood & cancer 62 (8), 1481-1484, 2015 | 23 | 2015 |
| High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers M González-Acosta, F Marín, B Puliafito, N Bonifaci, A Fernández, ... Journal of medical genetics 57 (4), 269-273, 2020 | 19 | 2020 |
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