متابعة
Christian Kratz
Christian Kratz
انتساب غير معروف
بريد إلكتروني تم التحقق منه على mh-hannover.de
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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
16752022
The landscape of genomic alterations across childhood cancers
SN Gröbner, BC Worst, J Weischenfeldt, I Buchhalter, K Kleinheinz, ...
Nature 555 (7696), 321-327, 2018
12742018
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
8502006
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
6912017
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
6642012
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
5652008
Medulloblastoma
PA Northcott, GW Robinson, CP Kratz, DJ Mabbott, SL Pomeroy, ...
Nature reviews Disease primers 5 (1), 11, 2019
5132019
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
4562017
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
4322014
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
3892009
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
3792018
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
3512018
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
3512010
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
2972017
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
2952005
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
2482018
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
2392015
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
2322011
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
M Zenker, K Lehmann, AL Schulz, H Barth, D Hansmann, R Koenig, ...
Journal of medical genetics 44 (2), 131-135, 2007
2262007
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
2142015
يتعذر على النظام إجراء العملية في الوقت الحالي. عاود المحاولة لاحقًا.
مقالات 1–20