What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
His primary areas of study are Immunology, Germinal center, B cell, Cellular differentiation and Cell biology.
His work is connected to Antigen, Antibody, Autoimmunity, Humoral immunity and Adoptive cell transfer, as a part of Immunology.
His Germinal center study incorporates themes from Plasma cell, Molecular biology, CD40 and Follicular dendritic cells.
His B cell study which covers B-1 cell that intersects with Naive B cell.
His Cellular differentiation study deals with B-cell activating factor intersecting with Rheumatoid arthritis, T cell and Cell signaling.
His Cell biology research incorporates themes from Inhibitor of apoptosis, Programmed cell death, TRAF2 and Autocrine signalling.
His most cited work include:
- Altered immunoglobulin expression and functional silencing of self-reactive B lymphocytes in transgenic mice (1127 citations)
- IAP Antagonists Target cIAP1 to Induce TNFα-Dependent Apoptosis (879 citations)
- Elimination from peripheral lymphoid tissues of self-reactive B lymphocytes recognizing membrane-bound antigens. (617 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Immunology, Cell biology, Germinal center, B cell and Antigen.
His Cell biology research incorporates elements of Receptor, B-cell activating factor, Cellular differentiation and CD40.
His work is dedicated to discovering how CD40, Antigen-presenting cell are connected with Interleukin 21 and other disciplines.
Robert Brink interconnects Plasma cell, Somatic hypermutation, Affinity maturation, Molecular biology and Naive B cell in the investigation of issues within Germinal center.
His studies in B cell integrate themes in fields like C-C chemokine receptor type 7, CXCL13 and B-1 cell.
As a part of the same scientific family, Robert Brink mostly works in the field of Antigen, focusing on Antibody and, on occasion, Virology, Cytoplasm and breakpoint cluster region.
He most often published in these fields:
- Immunology (72.99%)
- Cell biology (67.77%)
- Germinal center (69.67%)
What were the highlights of his more recent work (between 2018-2021)?
- Germinal center (69.67%)
- B cell (57.35%)
- Cell biology (67.77%)
In recent papers he was focusing on the following fields of study:
Robert Brink spends much of his time researching Germinal center, B cell, Cell biology, Antibody and Immunology.
His work deals with themes such as Plasma cell, Somatic hypermutation and Antigen, which intersect with Germinal center.
His research integrates issues of Molecular biology, Protein subunit, Caenorhabditis elegans and Cell cycle in his study of B cell.
The study incorporates disciplines such as Osteoclast, Osteoprotegerin and RANKL in addition to Cell biology.
His study focuses on the intersection of Antibody and fields such as Mutation with connections in the field of Allele, Transgene, Acquired immune system and Virology.
His studies deal with areas such as Gene silencing and MEDLINE as well as Immunology.
Between 2018 and 2021, his most popular works were:
- Lymphoma Driver Mutations in the Pathogenic Evolution of an Iconic Human Autoantibody (21 citations)
- Lymphoma Driver Mutations in the Pathogenic Evolution of an Iconic Human Autoantibody (21 citations)
- Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity. (21 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
Robert Brink mainly focuses on Immune system, Germinal center, Antibody, Mutation and Plasma cell.
His Immune system study integrates concerns from other disciplines, such as TNFAIP3, Cancer research, Transgene and Germline mutation.
His Germinal center study incorporates themes from Somatic hypermutation, Antigen, Memory B cell and Cell biology.
The Antibody study combines topics in areas such as Gene and Virology.
His Mutation research includes elements of Acquired immune system, Immunity, Allele and Phosphorylation.
His research in Plasma cell intersects with topics in Carboxyfluorescein succinimidyl ester, Cytokine, CD8, CXCR3 and FOXP3.
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