Reinhard Schneppenheim
Publications by Year
Research Areas
Platelet Disorders and Treatments, Blood groups and transfusion, Complement system in diseases, Blood disorders and treatments, Chromatin Remodeling and Cancer
Most-Cited Works
- → Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor(2006)1,132 cited
- → New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs(2016)992 cited
- → Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes(2016)564 cited
- → A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)(2006)524 cited
- → Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)(2006)398 cited
- → Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome(1997)334 cited
- → Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome(2010)333 cited
- → Molecular Analysis of the SGLT2 Gene in Patients with Renal Glucosuria(2003)298 cited
- → Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A(2005)277 cited
- → Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology(2017)273 cited