H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Immunology D-index 78 Citations 25,878 209 World Ranking 714 National Ranking 33
Medicine D-index 86 Citations 29,532 261 World Ranking 7203 National Ranking 335

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Immune system

Bodo Grimbacher focuses on Immunology, Common variable immunodeficiency, Immunodeficiency, Primary immunodeficiency and Hypogammaglobulinemia. His research integrates issues of Mutation and Genetics in his study of Immunology. His Common variable immunodeficiency research is multidisciplinary, relying on both Enteropathy, T cell, Selective IgA deficiency, Autoimmunity and B-cell activating factor.

Within one scientific family, Bodo Grimbacher focuses on topics pertaining to Hematopoietic stem cell transplantation under Immunodeficiency, and may sometimes address concerns connected to Inflammatory bowel disease and Colitis. He interconnects Genotype, Molecular biology, Immune system and Antigen in the investigation of issues within Hypogammaglobulinemia. His biological study spans a wide range of topics, including Dock8 and Hyperimmunoglobulin E syndrome.

His most cited work include:

  • Inflammatory bowel disease and mutations affecting the interleukin-10 receptor. (1005 citations)
  • STAT3 Mutations in the Hyper-IgE Syndrome (894 citations)
  • Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency (627 citations)

What are the main themes of his work throughout his whole career to date?

His primary scientific interests are in Immunology, Common variable immunodeficiency, Primary immunodeficiency, Immunodeficiency and Genetics. His Immunology research integrates issues from Hematopoietic stem cell transplantation and Disease. His Hematopoietic stem cell transplantation study incorporates themes from DOCK8 Deficiency and Inflammatory bowel disease.

His work in Common variable immunodeficiency covers topics such as B cell which are related to areas like Molecular biology. His research in Primary immunodeficiency intersects with topics in T cell, Immune dysregulation, Chronic mucocutaneous candidiasis and Pediatrics. His studies deal with areas such as Missense mutation, Internal medicine and Virology as well as Immunodeficiency.

He most often published in these fields:

  • Immunology (83.23%)
  • Common variable immunodeficiency (44.01%)
  • Primary immunodeficiency (28.74%)

What were the highlights of his more recent work (between 2016-2021)?

  • Immunology (83.23%)
  • Common variable immunodeficiency (44.01%)
  • Primary immunodeficiency (28.74%)

In recent papers he was focusing on the following fields of study:

Bodo Grimbacher mainly focuses on Immunology, Common variable immunodeficiency, Primary immunodeficiency, Immunodeficiency and Immune dysregulation. The various areas that Bodo Grimbacher examines in his Immunology study include Penetrance and Hematopoietic stem cell transplantation. The Common variable immunodeficiency study combines topics in areas such as Hypogammaglobulinemia, Internal medicine, Disease, Cohort and Pediatrics.

His Primary immunodeficiency study combines topics in areas such as Immunophenotyping, Peripheral blood and Receiver operating characteristic. His Immunodeficiency research is multidisciplinary, incorporating elements of Missense mutation, Compound heterozygosity, Progressive multifocal leukoencephalopathy and STAT3, Glycoprotein 130. His study on Immune dysregulation also encompasses disciplines like

  • Germline mutation, Mutation and Antibody most often made with reference to CTLA-4,
  • Phenotype that intertwine with fields like T helper 17 cell, Immunocompetence and Germline.

Between 2016 and 2021, his most popular works were:

  • Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study. (182 citations)
  • Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects (132 citations)
  • Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects (132 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Immune system

His primary areas of study are Immunology, Common variable immunodeficiency, Primary immunodeficiency, Immune dysregulation and Immunodeficiency. He studies Autoimmunity which is a part of Immunology. The concepts of his Common variable immunodeficiency study are interwoven with issues in Guideline, Antibiotics and Disease.

Bodo Grimbacher focuses mostly in the field of Primary immunodeficiency, narrowing it down to matters related to Cohort and, in some cases, Pediatrics, Risk factor, Disease burden and Comorbidity. His work carried out in the field of Immune dysregulation brings together such families of science as CTLA-4, Loss function, Immunosuppression and Hypogammaglobulinemia. His Immunodeficiency study integrates concerns from other disciplines, such as Missense mutation, Interleukin 6, Leukemia inhibitory factor, Oncostatin M and Cytokine receptor.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

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

Erik-Oliver Glocker;Daniel Kotlarz;Kaan Boztug;E. Michael Gertz.
The New England Journal of Medicine (2009)

1335 Citations

STAT3 Mutations in the Hyper-IgE Syndrome

Steven M. Holland;Frank R. DeLeo;Houda Z. Elloumi;Amy P. Hsu.
The New England Journal of Medicine (2007)

1164 Citations

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

Bodo Grimbacher;Steven M. Holland;John I. Gallin;Frank Greenberg.
The New England Journal of Medicine (1999)

820 Citations

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

Bodo Grimbacher;Andreas Hutloff;Michael Schlesier;Erik Glocker.
Nature Immunology (2003)

793 Citations

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

Erik-Oliver Glocker;Andre Hennigs;Mohammad Nabavi;Alejandro A. Schäffer.
The New England Journal of Medicine (2009)

737 Citations

Common variable immunodeficiency disorders: division into distinct clinical phenotypes

Helen Chapel;Mary Lucas;Martin Lee;Janne Bjorkander.
Blood (2008)

731 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.
Nature Genetics (2005)

679 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.
Journal of Experimental Medicine (2008)

663 Citations

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.

Desireé Schubert;Desireé Schubert;Claudia Bode;Rupert Kenefeck;Tie Zheng Hou.
Nature Medicine (2014)

595 Citations

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

Menno C van Zelm;Ismail Reisli;Mirjam van der Burg;Diana Castaño.
The New England Journal of Medicine (2006)

552 Citations

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