Mihály Józsi

Overview

Best Publications

• Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

  Timothy H.J. Goodship;H. Terence Cook;Fadi Fakhouri;Fernando C. Fervenza

  741
  Citations

• Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

  Mihály Józsi;Christoph Licht;Stefanie Strobel;Svante L. H. Zipfel

  414
  Citations

• Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

  Tamara Manuelian;Jens Hellwage;Seppo Meri;Jessica Caprioli

  410
  Citations

• Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

  Peter F Zipfel;Matthew Edey;Stefan Heinen;Mihály Józsi

  401
  Citations

• C3 glomerulopathy — understanding a rare complement-driven renal disease

  Richard J.H. Smith;Gerald B. Appel;Anna M. Blom;H. Terence Cook

  386
  Citations

• Factor H family proteins and human diseases.

  Mihály Józsi;Peter F. Zipfel;Peter F. Zipfel

  317
  Citations

• Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

  Maria Asuncion Abrera-Abeleda;Carla Nishimura;Jenna L.H. Smith;Sanjjev Sethi

  301
  Citations

• Anti–factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome

  Mihály Józsi;Stefanie Strobel;Hans-Martin Dahse;Wei-shih Liu

  285
  Citations

• Complement and diseases: defective alternative pathway control results in kidney and eye diseases.

  Peter F. Zipfel;Stefan Heinen;Mihály Józsi;Christine Skerka

  262
  Citations

• Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

  C. Licht;S. Heinen;M. Józsi;I. Löschmann

  256
  Citations

• The C‐terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein

  M. Oppermann;T. Manuelian;M. Józsi;E. Brandt

  191
  Citations

• Factor H and Atypical Hemolytic Uremic Syndrome: Mutations in the C-Terminus Cause Structural Changes and Defective Recognition Functions

  Mihály Józsi;Stefan Heinen;Andrea Hartmann;Clemens W. Ostrowicz

  158
  Citations

• Factor H-related proteins determine complement-activating surfaces.

  Mihály Józsi;Agustin Tortajada;Barbara Uzonyi;Elena Goicoechea de Jorge;Elena Goicoechea de Jorge

  157
  Citations

• Leptospiral immunoglobulin-like proteins interact with human complement regulators Factor H, FHL-1, FHR-1, and C4BP

  Mónica Marcela Castiblanco-Valencia;Tatiana Rodrigues Fraga;Ludmila Bezerra da Silva;Denize Monaris

  156
  Citations

• Factor h: a complement regulator in health and disease, and a mediator of cellular interactions.

  Anne Kopp;Mario Hebecker;Eliška Svobodová;Mihály Józsi

  151
  Citations

• Monomeric CRP contributes to complement control in fluid phase and on cellular surfaces and increases phagocytosis by recruiting factor H

  M Mihlan;S Stippa;M Józsi;P F Zipfel;P F Zipfel

  150
  Citations

• Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site.

  T. Sakari Jokiranta;Zhu Zhu Cheng;Harald Seeberger;Mihály Jòzsi

  149
  Citations

• Anti-factor B autoantibody in dense deposit disease.

  Stefanie Strobel;Miriam Zimmering;Krisztián Papp;József Prechl

  142
  Citations

• The C-terminus of complement factor H is essential for host cell protection.

  Mihály Józsi;Martin Oppermann;John D. Lambris;Peter F. Zipfel;Peter F. Zipfel

  131
  Citations

• Factor H and Factor H-Related Protein 1 Bind to Human Neutrophils via Complement Receptor 3, Mediate Attachment to Candida albicans, and Enhance Neutrophil Antimicrobial Activity

  Josephine Losse;Peter F. Zipfel;Peter F. Zipfel;Mihály Józsi

  130
  Citations