His primary scientific interests are in Cancer, Germline mutation, Genetics, Noonan syndrome and Pathology. Cancer is a subfield of Internal medicine that Christian P. Kratz investigates. His biological study spans a wide range of topics, including Medulloblastoma and Li–Fraumeni syndrome.
The Germline mutation study combines topics in areas such as Immunology, Malignancy, Pediatrics and Lynch syndrome. His Noonan syndrome research is multidisciplinary, incorporating elements of KRAS, Costello syndrome, PTPN11 and Ectodermal dysplasia. The concepts of his Pathology study are interwoven with issues in Congenital Neutropenia, HAX1, Genetic linkage, Leukemia and Candidate gene.
Christian P. Kratz focuses on Internal medicine, Oncology, Cancer, Genetics and Immunology. His Internal medicine study integrates concerns from other disciplines, such as Bone marrow failure and Li–Fraumeni syndrome. As part of the same scientific family, Christian P. Kratz usually focuses on Oncology, concentrating on Genotype and intersecting with Young adult.
The study incorporates disciplines such as Genetic counseling, Epidemiology and Human genetics in addition to Cancer. His Leukemia study in the realm of Immunology connects with subjects such as In patient. His Germline mutation study incorporates themes from Pathology, MSH2, DNA mismatch repair and Microsatellite instability.
His primary areas of investigation include Internal medicine, Cancer, Oncology, Genetic counseling and Germline mutation. His Internal medicine study frequently intersects with other fields, such as Genotype. His studies deal with areas such as Epidemiology, Host genome and Intensive care medicine as well as Cancer.
His Oncology research includes themes of Childhood Cancer Registry, Li–Fraumeni syndrome, Germline and Ovarian Teratoma, Ovary. To a larger extent, Christian P. Kratz studies Genetics with the aim of understanding Genetic counseling. His research in Germline mutation intersects with topics in Hemophagocytic lymphohistiocytosis, Hematopoietic stem cell transplantation, Microsatellite instability and DNA mismatch repair.
Christian P. Kratz mainly focuses on Internal medicine, Oncology, Germline mutation, Genotype and Cancer. His Oncology study combines topics from a wide range of disciplines, such as Germ cell tumors, Stage and Ovarian Teratoma, Ovary. His Germline mutation research integrates issues from Differential diagnosis, Pediatrics, Germline and Medical genetics.
In his study, Microsatellite, DNA mismatch repair, Microsatellite instability and Lynch syndrome is inextricably linked to DNA sequencing, which falls within the broad field of Germline. His work carried out in the field of Genotype brings together such families of science as Hepatoblastoma, Observational study, Retrospective cohort study and Childhood Cancer Registry. Christian P. Kratz has included themes like Phenotype, Telomere biology and Cohort in his Cancer study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The landscape of genomic alterations across childhood cancers
Susanne N. Gröbner;Barbara C. Worst;Joachim Weischenfeldt;Joachim Weischenfeldt;Ivo Buchhalter.
Nature (2018)
Germline KRAS mutations cause Noonan syndrome
Suzanne Schubbert;Martin Zenker;Sara L . Rowe;Silke Böll.
Nature Genetics (2006)
Detectable clonal mosaicism and its relationship to aging and cancer
Kevin B. Jacobs;Kevin B. Jacobs;Meredith Yeager;Meredith Yeager;Weiyin Zhou;Weiyin Zhou;Sholom Wacholder.
Nature Genetics (2012)
Comprehensive Analysis of Hypermutation in Human Cancer
Brittany B. Campbell;Nicholas Light;David Fabrizio;Matthew Zatzman.
Cell (2017)
BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas
Stefan Pfister;Wibke G. Janzarik;Marc Remke;Aurélie Ernst.
Journal of Clinical Investigation (2008)
Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome
Christian P. Kratz;Maria Isabel Achatz;Laurence Brugieres;Thierry Frebourg.
Clinical Cancer Research (2017)
A Syndrome with Congenital Neutropenia and Mutations in G6PC3
Kaan Boztug;Giridharan Appaswamy;Angel Ashikov;Alejandro A. Schäffer.
The New England Journal of Medicine (2009)
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)
Katharina Wimmer;Christian P Kratz;Hans F A Vasen;Olivier Caron.
Journal of Medical Genetics (2014)
A restricted spectrum of NRAS mutations causes Noonan syndrome
Ion C. Cirstea;Kerstin Kutsche;Radovan Dvorsky;Lothar Gremer.
Nature Genetics (2010)
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease
Christian P. Kratz;Charlotte M. Niemeyer;Robert P. Castleberry;Mualla Cetin.
Blood (2005)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Freiburg
Otto-von-Guericke University Magdeburg
German Cancer Research Center
National Institutes of Health
Aarhus University Hospital
National Institutes of Health
University of California, San Francisco
University of Pavia
National Institutes of Health
Hannover Medical School
Northeastern University
Umeå University
École Nationale de la Statistique et de l'Administration Économique
Monash University
Fudan University
University of Glasgow
Nanjing University of Aeronautics and Astronautics
Trinity College Dublin
Centre national de la recherche scientifique, CNRS
Johannes Gutenberg University of Mainz
University of Colorado Boulder
Jaume I University
University of California, Irvine
New York University
European Southern Observatory
University of Hawaii System