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Reinhard Schneppenheim

Reinhard Schneppenheim

D-Index & Metrics

Biology and Biochemistry

D-Index
68
Citations
17383
World Ranking
7760
National Ranking
568

Overview

Reinhard Schneppenheim is affiliated with Universität Hamburg in Germany and conducts research primarily within the field of Medicine, with a focus on Hematology. Their work covers several significant subfields including Genetics, Immunology, Surgery, and Pulmonary and Respiratory Medicine.

Their research topics encompass a variety of areas related to blood and coagulation disorders, such as Platelet Disorders and Treatments, Blood groups and transfusion, Complement system in diseases, Blood properties and coagulation, Coagulation, Bradykinin, Polyphosphates, and Angioedema, Heparin-Induced Thrombocytopenia and Thrombosis, and other Blood disorders and treatments.

Schneppenheim has contributed to multiple publications in venues commonly associated with hematology and blood research. Frequent publication venues include:

  • Hämostaseologie
  • Journal of Thrombosis and Haemostasis
  • Blood
  • Research Square (Research Square)
  • Blood Advances

Their recent publications illustrate a focus on complex blood-related diseases and their genetic and clinical risk factors. Selected recent papers are:

  • Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS-IPS, an international and collaborative cross-sectional study (2020), Journal of Thrombosis and Haemostasis
  • Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK) (2020), European Journal of Cancer
  • Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS (2021), Blood Advances
  • Platelet adhesion and aggregate formation controlled by immobilised and soluble VWF (2020), BMC Molecular and Cell Biology
  • von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS (2023), Journal of Thrombosis and Haemostasis

Throughout their research career, Schneppenheim has frequently collaborated with fellow researchers, with notable co-authors including Tobias Obser, Paul Knöbl, Masanori Matsumoto, Bernhard Lämmle, and Ulrich Budde. These collaborations have often intersected in producing work on blood disorders and coagulation.

Best Publications

  • Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

    J E Sadler;U Budde;J C J Eikenboom;E J Favaloro

  • New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs

    Dominik Sturm;Dominik Sturm;Brent A. Orr;Umut H. Toprak;Volker Hovestadt

  • Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

    Udo zur Stadt;Susanne Schmidt;Brigitte Kasper;Karin Beutel

  • A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)

    A Tosetto;F Rodeghiero;G Castaman;A Goodeve

  • 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)

    Anne C. Goodeve;Jeroen Eikenboom;Giancarlo Castaman;Francesco Rodeghiero

  • Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes

    Pascal D. Johann;Pascal D. Johann;Serap Erkek;Marc Zapatka;Kornelius Kerl

  • Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome

    Reinhard Schneppenheim;Michael C. Frühwald;Stefan Gesk;Martin Hasselblatt

  • Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome.

    René Santer;Reinhard Schneppenheim;Anja Dombrowski;Hermann Götze

  • Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.

    Udo Zur Stadt;Karin Beutel;Susanne Kolberg;Reinhard Schneppenheim

  • von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.

    Reinhard Schneppenheim;Ulrich Budde;Florian Oyen;Dorothea Angerhaus

  • Childhood cancer predisposition syndromes : A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

    Tim Ripperger;Stefan S. Bielack;Arndt Borkhardt;Ines B. Brecht;Ines B. Brecht

  • Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression

    Martin Hasselblatt;Stefan Gesk;Florian Oyen;Sabrina Rossi

  • Haemophilia A: from mutation analysis to new therapies

    Jochen Graw;Hans-Hermann Brackmann;Johannes Oldenburg;Reinhard Schneppenheim

  • Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD) : results from the European Study MCMDM-1VWD

    Giancarlo Castaman;Stefan Lethagen;Augusto B. Federici;Alberto Tosetto

  • Recombinant ADAMTS-13: First-in-human pharmacokinetics and safety in congenital thrombotic thrombocytopenic purpura

    Marie Scully;Paul Knöbl;Karim Kentouche;Lawrence Rice

  • Update on von Willebrand factor multimers: focus on high-molecular-weight multimers and their role in hemostasis.

    Marcus Stockschlaeder;Reinhard Schneppenheim;Ulrich Budde

  • Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism.

    U. Nowak‐Göttl;H. G. Koch;I. Aschka;B. Kohlhase

  • Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)

    U Budde;R Schneppenheim;J Eikenboom;A Goodeve

  • Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).

    Sandra L. Haberichter;Sandra L. Haberichter;Sandra L. Haberichter;Giancarlo Castaman;Ulrich Budde;Ian Peake

  • Denosumab: a potential new and innovative treatment option for aneurysmal bone cysts

    Tobias Lange;Christoph Stehling;Birgit Fröhlich;Mark Klingenhöfer

Frequent Co-Authors

Reiner Siebert
Reiner Siebert University of Ulm
Marcel Kool
Marcel Kool German Cancer Research Center
Stefan M. Pfister
Stefan M. Pfister German Cancer Research Center
Johannes Oldenburg
Johannes Oldenburg University of Bonn
David Capper
David Capper Charité - University Medicine Berlin
Francesco Rodeghiero
Francesco Rodeghiero Yamagata University
Werner Paulus
Werner Paulus University of Münster
Norbert Graf
Norbert Graf Saarland University
Lars Holmberg
Lars Holmberg King's College London
Ulrich Schüller
Ulrich Schüller Universität Hamburg

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