Author details

Full Name

Christian P Kratz

Affiliation

ORCID

Career Start Year

1998

Papers

191

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34331184	Unusual phenotypes in patients with a pathogenic germline variant in DICER1.	Fam Cancer	2023
36651980	Molecular complete remission following combination treatment of daratumumab and venetoclax in an adolescent with relapsed mixed phenotype acute leukemia.		2023
36586540	Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency.	Gastroenterology	2023
36647321	Comments on "The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients".		2023
36764384	Genetic susceptibility in children, adolescents, and young adults diagnosed with soft-tissue sarcomas.	Eur J Med Genet	2023
36639636	Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group.	J Exp Clin Cancer Res	2023
36495208	Reply to Evans and Woodward.	J Natl Cancer Inst	2023
37066598	Second-line treatment of pediatric patients with relapsed rhabdomyosarcoma adapted to initial risk stratification: Data of the European Soft Tissue Sarcoma Registry (SoTiSaR).	Pediatr Blood Cancer	2023
37004196	Reply to Li and Colleagues.	J Natl Cancer Inst	2023
37379234	Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome.	Neuro Oncol	2023
36612313	Epidemiology and Characteristics of Gastric Carcinoma in Childhood-An Analysis of Data from Population-Based and Clinical Cancer Registries.	Cancers (Basel)	2023
37351819	Willingness of individuals with Li-Fraumeni syndrome to participate in a cancer prevention trial: a survey study.		2023
34597127	Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia-A Nationwide Register-Based Cohort Study in Germany.	Journal of Clinical Oncology	2022
35974385	Genotype-phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry.	J Hematol Oncol	2022
35768194	Cancer risk and tumour spectrum in 172 patients with a germline <i>SUFU</i> pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.	J Med Genet	2022
35446794	SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome.	Am J Surg Pathol	2022
36290891	Health Behavior and Cancer Prevention among Adults with Li-Fraumeni Syndrome and Relatives in Germany-A Cohort Description.	Current Oncology	2022
36166074	[Li-Fraumeni syndrome].		2022
35804856	Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.	Cancers	2022
35732831	The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/DendriticÂ Neoplasms.	Leukemia	2022
35790048	WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly.	Hum Mutat	2022
36191386	Osteosarcoma and causes of death: A report of 1520 deceased patients from the Cooperative Osteosarcoma Study Group (COSS).	Eur J Cancer	2022
35980168	Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer.	J Natl Cancer Inst	2022
35352025	The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute.	Cell Death Differ	2022
36533693	Cancer incidence and surveillance strategies in individuals with RASopathies.	Am J Med Genet C Semin Med Genet	2022
34921008	A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era.	Cancer Discov	2022
35027859	Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline.	Geburtshilfe und Frauenheilkunde	2022
34709361	Analysis of the Li-Fraumeni Spectrum Based on an International Germline TP53 Variant Data Set: An International Agency for Research on Cancer TP53 Database Analysis.	JAMA Oncol	2021
33860896	Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG).	Fam Cancer	2021
33484663	Predisposition to cancer in children and adolescents.	Lancet Child Adolesc Health	2021
33751320	Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer.	Fam Cancer	2021
33634344	Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features.	Familial Cancer	2021
33532948	Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.	Fam Cancer	2021
33580201	Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li-Fraumeni syndrome.	Leukemia	2021
33576909	Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer.	Fam Cancer	2021
33945292	Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance.	J Clin Oncol	2021
34196171	A novel classification of hematologic conditions in patients with Fanconi anemia.	Haematologica	2021
33714975	Hepatic sinusoidal obstruction syndrome and short-term application of 6-thioguanine in pediatric acute lymphoblastic leukemia.	Leukemia	2021
34134020	Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group.	Eur J Cancer	2021
33651299	Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire.	Familial Cancer	2021
33919815	Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria.	Cancers (Basel)	2021
32971146	Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders.	J Pediatr	2021
33216206	Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis.	Acta Neuropathol	2021
32888134	Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group.	Fam Cancer	2021
34569185	Breast cancer characteristics and surgery among women with Li-Fraumeni syndrome in Germany-A retrospective cohort study.	Cancer Med	2021
34768335	Genetic Variation in <i>ABCC4</i> and <i>CFTR</i> and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia.	J Clin Med	2021
31494577	High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers.	Journal of Medical Genetics	2020
32067684	Extended induction chemotherapy does not improve the outcome for high-risk neuroblastoma patients: results of the randomized open-label GPOH trial NB2004-HR.	Ann Oncol	2020
32005112	Social inequalities in the participation and activity of children and adolescents with leukemia, brain tumors, and sarcomas (SUPATEEN): a protocol for a multicenter longitudinal prospective observational study.	BMC Pediatr	2020
32285995	TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosis.	Pediatric Blood and Cancer	2020