D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Immunology D-index 84 Citations 23,654 240 World Ranking 867 National Ranking 486

Overview

What is he best known for?

The fields of study he is best known for:

  • Immune system
  • Cytokine
  • T cell

T cell, Cell biology, Immunology, Cytotoxic T cell and Antigen-presenting cell are his primary areas of study. His work in T cell tackles topics such as Apoptosis which are related to areas like Intracellular. His study in Cell biology is interdisciplinary in nature, drawing from both Receptor, Cytokine and T-cell receptor.

His study connects CD40 and Immunology. His Cytotoxic T cell research is multidisciplinary, incorporating perspectives in Priming and CD8. As a part of the same scientific family, he mostly works in the field of Antigen-presenting cell, focusing on Molecular biology and, on occasion, Dendritic cell, Leukotriene E4, Leukotriene D4 and Leukotriene.

His most cited work include:

  • Co-stimulatory members of the TNFR family: keys to effective T-cell immunity? (760 citations)
  • The role of TNF superfamily members in T-cell function and diseases (594 citations)
  • OX40 promotes Bcl-xL and Bcl-2 expression and is essential for long-term survival of CD4 T cells. (557 citations)

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

The scientist’s investigation covers issues in Immunology, Cell biology, T cell, Cytotoxic T cell and Immune system. His Immunology study frequently draws connections to adjacent fields such as CD40. His Cell biology study incorporates themes from CD28, Receptor and T-cell receptor.

In general T cell study, his work on CD134 and Naive T cell often relates to the realm of Cellular differentiation and Population, thereby connecting several areas of interest. The various areas that Michael Croft examines in his Cytotoxic T cell study include CD8 and Virology. His Antigen-presenting cell research is multidisciplinary, incorporating elements of Molecular biology, Interleukin 12, Priming and Antigen presentation.

He most often published in these fields:

  • Immunology (57.53%)
  • Cell biology (40.15%)
  • T cell (31.66%)

What were the highlights of his more recent work (between 2017-2021)?

  • Cancer research (13.13%)
  • Immunology (57.53%)
  • Inflammation (21.24%)

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

His primary areas of study are Cancer research, Immunology, Inflammation, Tumor necrosis factor alpha and Receptor. His study in Allergen, T cell, Hepatitis B, Innate immune system and Hepatitis B virus is carried out as part of his studies in Immunology. His research links CD40 with T cell.

His work deals with themes such as Bronchoalveolar lavage, Signal transduction, Cytokine and Hepatocyte, which intersect with Inflammation. His Receptor research is multidisciplinary, relying on both Intramolecular force and Cell biology. Michael Croft combines subjects such as Transfection and Conditional gene knockout with his study of Cell biology.

Between 2017 and 2021, his most popular works were:

  • TNF activity and T cells (87 citations)
  • An OX40/OX40L interaction directs successful immunity to hepatitis B virus (18 citations)
  • TNFSF14 (LIGHT) Exhibits Inflammatory Activities in Lung Fibroblasts Complementary to IL-13 and TGF-β. (18 citations)

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

  • Immune system
  • Cytokine
  • Antibody

Michael Croft mostly deals with Tumor necrosis factor alpha, Immunology, Cancer research, Cytotoxic T cell and Receptor. His work deals with themes such as Liver injury and CD40, which intersect with Immunology. His Cancer research study combines topics in areas such as Cancer, Cytokine, Lymphotoxin, Monoclonal and Inflammation.

Michael Croft interconnects Humanized mouse, Tumor necrosis factor receptor 2, Antibody and Cancer immunotherapy in the investigation of issues within Cytotoxic T cell. His Receptor study combines topics from a wide range of disciplines, such as Protein structure, CD137, Binding site and Protein–protein interaction. His specific area of interest is T cell, where Michael Croft studies IL-2 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

Co-stimulatory members of the TNFR family: keys to effective T-cell immunity?

Michael Croft.
Nature Reviews Immunology (2003)

1232 Citations

The role of TNF superfamily members in T-cell function and diseases

Michael Croft.
Nature Reviews Immunology (2009)

1019 Citations

Ox-40 Ligand: A Potent Costimulatory Molecule for Sustaining Primary CD4 T Cell Responses

Irene Gramaglia;Andrew D. Weinberg;Michael Lemon;Michael Croft.
Journal of Immunology (1998)

740 Citations

Naive versus memory CD4 T cell response to antigen. Memory cells are less dependent on accessory cell costimulation and can respond to many antigen-presenting cell types including resting B cells.

M Croft;L M Bradley;S L Swain.
Journal of Immunology (1994)

722 Citations

Generation of polarized antigen-specific CD8 effector populations: reciprocal action of interleukin (IL)-4 and IL-12 in promoting type 2 versus type 1 cytokine profiles.

Michael Croft;Laura Carter;Susan L. Swain;Richard W. Dutton.
Journal of Experimental Medicine (1994)

651 Citations

OX40 promotes Bcl-xL and Bcl-2 expression and is essential for long-term survival of CD4 T cells.

Paul R Rogers;Jianxun Song;Irene Gramaglia;Nigel Killeen.
Immunity (2001)

599 Citations

Control of Immunity by the TNFR-Related Molecule OX40 (CD134)

Michael Croft.
Annual Review of Immunology (2010)

594 Citations

The OX40 costimulatory receptor determines the development of CD4 memory by regulating primary clonal expansion.

Irene Gramaglia;Amha Jember;Susanne D. Pippig;Andrew D. Weinberg.
Journal of Immunology (2000)

556 Citations

The Significance of OX40 and OX40L to T cell Biology and Immune Disease

Michael Croft;Takanori So;Wei Duan;Pejman Soroosh.
Immunological Reviews (2009)

548 Citations

Helper T-cell subsets: phenotype, function and the role of lymphokines in regulating their development.

Susan L. Swain;Linda M. Bradley;Michael Croft;Susan Tonkonogy.
Immunological Reviews (1991)

527 Citations

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