Hans-Hartmut Peter

Overview

Best Publications

• The EUROclass trial: defining subgroups in common variable immunodeficiency

  Claudia Wehr;Teemu Kivioja;Christian Schmitt;Berne Ferry

  979
  Citations

• Digital ulcers in systemic sclerosis: prevention by treatment with bosentan, an oral endothelin receptor antagonist.

  J. H. Korn;Maureen D Mayes;M. Matucci Cerinic;M. Rainisio

  904
  Citations

• Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

  Bodo Grimbacher;Andreas Hutloff;Michael Schlesier;Erik Glocker

  872
  Citations

• Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease.

  Klaus Warnatz;Axel Denz;Ruth Dräger;Moritz Braun

  859
  Citations

• Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

  U Salzer;H M Chapel;A D B Webster;Q Pan-Hammarström

  779
  Citations

• Human immunoglobulin M memory B cells controlling Streptococcus pneumoniae infections are generated in the spleen.

  Stephanie Kruetzmann;M. Manuela Rosado;Holger Weber;Ulrich Germing

  774
  Citations

• ICOS deficiency is associated with a severe reduction of CXCR5+CD4 germinal center Th cells.

  Lukas Bossaller;Jan Andreas Burger;Ruth Draeger;Bodo Grimbacher

  484
  Citations

• B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans

  Klaus Warnatz;Ulrich Salzer;Marta Rizzi;Beate Fischer

  426
  Citations

• Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells

  Mirzokhid Rakhmanov;Baerbel Keller;Sylvia Gutenberger;Christian Foerster

  379
  Citations

• A randomized trial of adjuvant chemotherapy and immunotherapy in cutaneous melanoma

  U. Veronesi;J. Adamus;C. Aubert;E. Bajetta

  359
  Citations

• A new CD21low B cell population in the peripheral blood of patients with SLE.

  Claudia Wehr;Hermann Eibel;Madhan Masilamani;Harald Illges

  356
  Citations

• Phase I/II trial of autologous stem cell transplantation in systemic sclerosis: procedure related mortality and impact on skin disease.

  M Binks;J. R. Passweg;D. Furst;P. Mcsweeney

  353
  Citations

• Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency.

  Klaus Warnatz;Lukas Bossaller;Ulrich Salzer;Andrea Skrabl-Baumgartner

  341
  Citations

• Autologous stem cell transplantation in the treatment of systemic sclerosis: Report from the EBMT/EULAR Registry

  D. Farge;J.R. Passweg;J.M. van Laar;Z. Marjanovic

  293
  Citations

• A New Type of Perinuclear Anti-Neutrophil Cytoplasmic Antibody (p-ANCA) in Active Ulcerative Colitis but not in Crohn's Disease

  Jörg A. Rump;Jürgen Schölmerich;Volker Gross;Michael Roth

  291
  Citations

• Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.

  Ulrich Salzer;Chiara Bacchelli;Sylvie Buckridge;Qiang Pan-Hammarström

  286
  Citations

• Magnetic resonance imaging (MRI) for detection of active sacroiliitis--a prospective study comparing conventional radiography, scintigraphy, and contrast enhanced MRI.

  U Blum;C Buitrago-Tellez;A Mundinger;T Krause

  277
  Citations

• Autologous haematopoietic stem cell transplants for autoimmune disease - feasibility and transplant-related mortality

  A Tyndall;A Fassas;J Passweg;C Ruiz de Elvira

  269
  Citations

• Expression of Matrix Metalloproteinases and Their Tissue Inhibitors in Human Brain Tumors

  Klaus Lampert;Uwe Machein;Márcia Regina Machein;Walter Conca

  260
  Citations

• Expansion of CD19hiCD21lo/neg B Cells in Common Variable Immunodeficiency (CVID) Patients with Autoimmune Cytopenia

  Klaus Warnatz;Claudia Wehr;Ruth Dräger;Sigune Schmidt

  240
  Citations

• Common variable immunodeficiency: an update.

  Ulrich Salzer;Klaus Warnatz;Hans Hartmut Peter

  231
  Citations

• Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

  U S Salzer;C Bacchelli;S Buckridge;Q Pan-Hammar-Strom

  4
  Citations