Tim Ripperger
Tim Ripperger
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Zitiert von
Zitiert von
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
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
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
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
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
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
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
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
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
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
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
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
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
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, ...
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
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
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
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
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
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
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