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
Biology and Biochemistry D-index 65 Citations 14,882 180 World Ranking 5897 National Ranking 2798

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Immune system

His main research concerns Major histocompatibility complex, Cell biology, Mucosal associated invariant T cell, T-cell receptor and Immunology. His research in Major histocompatibility complex intersects with topics in Cytotoxic T cell, Monoclonal antibody and T cell. His Cytotoxic T cell research is multidisciplinary, relying on both Beta-2 microglobulin and Virology.

Ted H. Hansen combines subjects such as Tapasin, Gene expression, T lymphocyte and CTL* with his study of Cell biology. The concepts of his Mucosal associated invariant T cell study are interwoven with issues in Cell activation, Natural killer T cell and Antigen presentation. His T-cell receptor research is multidisciplinary, incorporating perspectives in Molecular biology, Interleukin 12, CD8 and Cancer research.

His most cited work include:

  • Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages (1256 citations)
  • Licensing of natural killer cells by host major histocompatibility complex class I molecules (1057 citations)
  • Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells (451 citations)

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

Ted H. Hansen mostly deals with Major histocompatibility complex, MHC class I, Molecular biology, Cell biology and Antigen. Ted H. Hansen has researched Major histocompatibility complex in several fields, including CD8, T-cell receptor, Cytotoxic T cell, Antigen presentation and Peptide. His MHC class I research incorporates themes from DNA vaccination and Recombinant DNA.

His work carried out in the field of Molecular biology brings together such families of science as Ligand, T cell, Mutant, Gene and Antibody. His studies deal with areas such as Endoplasmic-reticulum-associated protein degradation, Tapasin, T lymphocyte and Genetics as well as Cell biology. His Antigen research includes themes of Monoclonal antibody and Immune system.

He most often published in these fields:

  • Major histocompatibility complex (41.81%)
  • MHC class I (31.64%)
  • Molecular biology (30.51%)

What were the highlights of his more recent work (between 2010-2021)?

  • Major histocompatibility complex (41.81%)
  • Antigen (27.12%)
  • Molecular biology (30.51%)

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

Ted H. Hansen spends much of his time researching Major histocompatibility complex, Antigen, Molecular biology, Virology and Antigen presentation. His Major histocompatibility complex study introduces a deeper knowledge of Gene. His studies in Molecular biology integrate themes in fields like Cell, MHC class I, T-cell receptor and Antibody, Monoclonal antibody.

The study incorporates disciplines such as Biophysics and Peptide in addition to MHC class I. As a member of one scientific family, Ted H. Hansen mostly works in the field of T-cell receptor, focusing on CD8 and, on occasion, T cell and Cytotoxic T cell. Antigen presentation is closely attributed to Cell biology in his study.

Between 2010 and 2021, his most popular works were:

  • Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages (1256 citations)
  • Antigen-loaded MR1 tetramers define T cell receptor heterogeneity in mucosal-associated invariant T cells (352 citations)
  • CD161 ++ CD8 + T cells, including the MAIT cell subset, are specifically activated by IL-12+IL-18 in a TCR-independent manner (314 citations)

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

Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages

Emmanuel L Gautier;Tal Shay;Tal Shay;Jennifer Miller;Melanie Greter.
Nature Immunology (2012)

1808 Citations

Licensing of natural killer cells by host major histocompatibility complex class I molecules

Sung Jin Kim;Jennifer Poursine-Laurent;Steven M. Truscott;Lonnie Lybarger.
Nature (2005)

1476 Citations

Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells

Marielle C. Gold;Marielle C. Gold;Stefania Cerri;Susan Smyk-Pearson;Meghan E. Cansler.
PLOS Biology (2010)

621 Citations

CD161 ++ CD8 + T cells, including the MAIT cell subset, are specifically activated by IL-12+IL-18 in a TCR-independent manner

James E. Ussher;Matthew Bilton;Emma Attwod;Jonathan Shadwell.
European Journal of Immunology (2014)

479 Citations

Antigen-loaded MR1 tetramers define T cell receptor heterogeneity in mucosal-associated invariant T cells

Rangsima Reantragoon;Alexandra Corbett;Isaac G Sakala;Nicholas A Gherardin;Nicholas A Gherardin.
Journal of Experimental Medicine (2013)

476 Citations

MHC class I antigen presentation: learning from viral evasion strategies

Ted H. Hansen;Marlene Bouvier.
Nature Reviews Immunology (2009)

433 Citations

Ubiquitination of serine, threonine, or lysine residues on the cytoplasmic tail can induce ERAD of MHC-I by viral E3 ligase mK3.

Xiaoli Wang;Roger A. Herr;Wei Jen Chua;Lonnie Lybarger.
Journal of Cell Biology (2007)

337 Citations

Early and nonreversible decrease of CD161++ /MAIT cells in HIV infection.

Cormac Cosgrove;James E. Ussher;Andri Rauch;Kathleen Gärtner.
Blood (2013)

316 Citations

Bcl-2 is upregulated at the CD4^+ CD8^+ stage during positive selection and promotes thymocyte differentiation at several control points

Gerald P. Linette;Michael J. Grusby;Stephen M. Hedrick;Ted H. Hansen.
Immunity (1994)

300 Citations

MAIT cells are licensed through granzyme exchange to kill bacterially sensitized targets

A Kurioka;J E Ussher;C Cosgrove;C Clough.
Mucosal Immunology (2015)

270 Citations

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