| The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms JD Khoury, E Solary, O Abla, Y Akkari, R Alaggio, JF Apperley, R Bejar, ... leukemia 36 (7), 1703-1719, 2022 | 2826 | 2022 |
| The landscape of genomic alterations across childhood cancers SN Gröbner, BC Worst, J Weischenfeldt, I Buchhalter, K Kleinheinz, ... Nature 555 (7696), 321-327, 2018 | 1492 | 2018 |
| Germline KRAS mutations cause Noonan syndrome S Schubbert, M Zenker, SL Rowe, S Böll, C Klein, G Bollag, ... Nature genetics 38 (3), 331-336, 2006 | 889 | 2006 |
| Comprehensive analysis of hypermutation in human cancer BB Campbell, N Light, D Fabrizio, M Zatzman, F Fuligni, R de Borja, ... Cell 171 (5), 1042-1056. e10, 2017 | 769 | 2017 |
| Detectable clonal mosaicism and its relationship to aging and cancer KB Jacobs, M Yeager, W Zhou, S Wacholder, Z Wang, ... Nature genetics 44 (6), 651-658, 2012 | 686 | 2012 |
| Medulloblastoma PA Northcott, GW Robinson, CP Kratz, DJ Mabbott, SL Pomeroy, ... Nature reviews Disease primers 5 (1), 11, 2019 | 606 | 2019 |
| BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas S Pfister, WG Janzarik, M Remke, A Ernst, W Werft, N Becker, G Toedt, ... The Journal of clinical investigation 118 (5), 1739-1749, 2008 | 594 | 2008 |
| Cancer screening recommendations for individuals with Li-Fraumeni syndrome CP Kratz, MI Achatz, L Brugieres, T Frebourg, JE Garber, MLC Greer, ... Clinical Cancer Research 23 (11), e38-e45, 2017 | 506 | 2017 |
| Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘care for CMMRD’(C4CMMRD) K Wimmer, CP Kratz, HFA Vasen, O Caron, C Colas, N Entz-Werle, ... Journal of medical genetics 51 (6), 355-365, 2014 | 480 | 2014 |
| Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. F Brioude, JM Kalish, A Mussa, AC Foster, J Bliek, GB Ferrero, ... Nat Rev Endocrinol 14 (4), 229-249, 2018 | 441 | 2018 |
| A Syndrome with Congenital Neutropenia and Mutations in G6PC3 K Boztug, G Appaswamy, A Ashikov, AA Schäffer, U Salzer, J Diestelhorst, ... New England Journal of Medicine 360 (1), 32-43, 2009 | 400 | 2009 |
| Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort SM Waszak, PA Northcott, I Buchhalter, GW Robinson, C Sutter, ... The Lancet Oncology 19 (6), 785-798, 2018 | 396 | 2018 |
| A restricted spectrum of NRAS mutations causes Noonan syndrome IC Cirstea, K Kutsche, R Dvorsky, L Gremer, C Carta, D Horn, AE Roberts, ... Nature genetics 42 (1), 27-29, 2010 | 369 | 2010 |
| 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 | 325 | 2017 |
| The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease CP Kratz, CM Niemeyer, RP Castleberry, M Cetin, E Bergsträsser, ... Blood 106 (6), 2183-2185, 2005 | 312 | 2005 |
| IKZF1plus Defines a New Minimal Residual Disease–Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia M Stanulla, E Dagdan, M Zaliova, A Möricke, C Palmi, G Cazzaniga, ... Journal of Clinical Oncology 36 (12), 1240-1249, 2018 | 297 | 2018 |
| Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options U Fischer, M Forster, A Rinaldi, T Risch, S Sungalee, HJ Warnatz, ... Nature genetics 47 (9), 1020-1029, 2015 | 274 | 2015 |
| Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes CP Kratz, S Rapisuwon, H Reed, H Hasle, PS Rosenberg American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2011 | 252 | 2011 |
| Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes CP Kratz, L Franke, H Peters, N Kohlschmidt, B Kazmierczak, U Finckh, ... British journal of cancer 112 (8), 1392-1397, 2015 | 246 | 2015 |
| Clinical management and tumor surveillance recommendations of inherited mismatch repair deficiency in childhood U Tabori, JR Hansford, MI Achatz, CP Kratz, SE Plon, T Frebourg, ... Clinical Cancer Research 23 (11), e32-e37, 2017 | 241 | 2017 |
