What is he best known for?
The fields of study he is best known for:
- Immune system
- Gene
- Cytokine
His primary scientific interests are in Immunology, Immune system, Interleukin 4, Innate immune system and Immunity.
Immunology and Cell biology are frequently intertwined in his study.
His Cell signaling study in the realm of Cell biology connects with subjects such as Chitin.
Interleukin 13 is closely connected to Immunoglobulin E in his research, which is encompassed under the umbrella topic of Immune system.
His Innate immune system study deals with Effector intersecting with Precursor cell, Genetically modified mouse, Lamina propria, Basophilia and In vivo.
His work carried out in the field of Immunity brings together such families of science as RAR-related orphan receptor gamma, T helper cell and Cell fate determination.
His most cited work include:
- Chitin induces accumulation in tissue of innate immune cells associated with allergy (598 citations)
- Chitin induces accumulation in tissue of innate immune cells associated with allergy (598 citations)
- The transcription factor GATA-3 controls cell fate and maintenance of type 2 innate lymphoid cells. (568 citations)
What are the main themes of his work throughout his whole career to date?
David Voehringer mostly deals with Immunology, Immune system, Cell biology, Immunoglobulin E and Interleukin 4.
Inflammation, Nippostrongylus brasiliensis, T cell, Basophil and Effector are the subjects of his Immunology studies.
His Immune system research includes themes of Eosinophil and Cell type.
His Cell biology research is multidisciplinary, incorporating perspectives in Receptor and Cytokine.
David Voehringer has researched Immunoglobulin E in several fields, including Acquired immune system, Germinal center, Secondary infection and Allergic inflammation.
The Interleukin 4 study combines topics in areas such as Adoptive cell transfer and Macrophage polarization.
He most often published in these fields:
- Immunology (69.75%)
- Immune system (39.50%)
- Cell biology (31.09%)
What were the highlights of his more recent work (between 2018-2021)?
- Inflammation (16.81%)
- Immunology (69.75%)
- Cell biology (31.09%)
In recent papers he was focusing on the following fields of study:
Inflammation, Immunology, Cell biology, Immune system and Immunoglobulin E are his primary areas of study.
The concepts of his Inflammation study are interwoven with issues in Eosinophilia, Eosinophil, Lung and Arthritis.
His Immunology study frequently links to adjacent areas such as Chemotaxis.
His work deals with themes such as Innate lymphoid cell and Bone marrow, which intersect with Cell biology.
His Immune system study incorporates themes from Helminths and Hookworm Infections.
His studies deal with areas such as Germinal center and Allergic inflammation as well as Immunoglobulin E.
Between 2018 and 2021, his most popular works were:
- Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition) (345 citations)
- Locally renewing resident synovial macrophages provide a protective barrier for the joint. (108 citations)
- RELMα-expressing macrophages protect against fatal lung damage and reduce parasite burden during helminth infection. (17 citations)
In his most recent research, the most cited papers focused on:
- Immune system
- Gene
- Cytokine
David Voehringer mainly focuses on Cell biology, Inflammation, Innate lymphoid cell, Immunology and Population.
His Cell biology study integrates concerns from other disciplines, such as Gene expression profiling, Arthritis, Ontogeny, Transcription factor and Bone marrow.
His Inflammation research integrates issues from Single-cell analysis, Peripheral blood mononuclear cell, Macrophage, MAPK/ERK pathway and Effector.
His Innate lymphoid cell study is concerned with Immune system in general.
His work on Immune system is being expanded to include thematically relevant topics such as Signal transduction.
The various areas that David Voehringer examines in his Immunology study include Cyclooxygenase, Chemotaxis and p38 mitogen-activated protein kinases.
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