Bodo Grimbacher

Bodo Grimbacher publication distribution in Immunology in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Immunology in 2026. The highlighted bar marks where Bodo Grimbacher sits on this spectrum.

Bodo Grimbacher D-index placement in Immunology in 2026

The chart shows the D-index (discipline H-index) distribution of Immunology scientists ranked by Research.com in 2026. The highlighted bar marks where Bodo Grimbacher sits on this spectrum.

Overview

Best Publications

• Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.

  Erik-Oliver Glocker;Daniel Kotlarz;Kaan Boztug;E. Michael Gertz

  1678
  Citations

• STAT3 Mutations in the Hyper-IgE Syndrome

  Steven M. Holland;Frank R. DeLeo;Houda Z. Elloumi;Amy P. Hsu

  1417
  Citations

• Common variable immunodeficiency disorders: division into distinct clinical phenotypes

  Helen Chapel;Mary Lucas;Martin Lee;Janne Bjorkander

  956
  Citations

• Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

  Bodo Grimbacher;Steven M. Holland;John I. Gallin;Frank Greenberg

  945
  Citations

• A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal Infections

  Erik-Oliver Glocker;Andre Hennigs;Mohammad Nabavi;Alejandro A. Schäffer

  909
  Citations

• Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.

  Desireé Schubert;Desireé Schubert;Claudia Bode;Rupert Kenefeck;Tie Zheng Hou

  894
  Citations

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

  Bodo Grimbacher;Andreas Hutloff;Michael Schlesier;Erik Glocker

  872
  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

• Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3

  Cindy S. Ma;Gary Y.J. Chew;Nicholas Simpson;Archana Priyadarshi

  779
  Citations

• Clinical picture and treatment of 2212 patients with common variable immunodeficiency

  Benjamin Gathmann;Nizar Mahlaoui;Laurence Gérard;Eric Oksenhendler

  709
  Citations

• B-cell biology and development

  Kathrin Pieper;Bodo Grimbacher;Hermann Eibel

  694
  Citations

• An antibody-deficiency syndrome due to mutations in the CD19 gene

  Menno C van Zelm;Ismail Reisli;Mirjam van der Burg;Diana Castaño

  622
  Citations

• Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

  Gabriela Lopez-Herrera;Giacomo Tampella;Qiang Pan-Hammarström;Peer Herholz

  591
  Citations

• Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

  Karin R. Engelhardt;Sean McGhee;Sabine Winkler;Atfa Sassi

  590
  Citations

• The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

  Markus G. Seidel;Gerhard Kindle;Benjamin Gathmann;Isabella Quinti

  588
  Citations

• HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

  Christoph Klein;Magda Grudzien;Giridharan Appaswamy;Manuela Germeshausen

  574
  Citations

• Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.

  Julie Toubiana;Satoshi Okada;Satoshi Okada;Julia Hiller;Matias Oleastro

  553
  Citations

• Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy.

  Daniel Kotlarz;Daniel Kotlarz;Rita Beier;Dhaarini Murugan;Dhaarini Murugan;Jana Diestelhorst;Jana Diestelhorst

  527
  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

• Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4

  Bodo Grimbacher;Alejandro A. Schäffer;Steven M. Holland;Joie Davis

  484
  Citations