2026 Ted H. Hansen: Biology and Biochemistry Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Biology and Biochemistry	69	7358	6784	3367	3024	222	17623

Overview

Ted H. Hansen is affiliated with Washington University in St. Louis in the United States. Their research primarily focuses on immunology, microbiology, and medicine, with notable work in biochemistry, genetics, and molecular biology.

The scientist's main fields of study include:

Immunology and Microbiology
Medicine
Biochemistry, Genetics and Molecular Biology

Subfields of research covered by Hansen are:

Immunology
Molecular Biology
Radiology, Nuclear Medicine and Imaging
Oncology
Epidemiology

The research topics frequently explored include:

Immunotherapy and Immune Responses
Vaccines and Immunoinformatics Approaches
Monoclonal and Polyclonal Antibodies Research
CAR-T Cell Therapy Research
Immune Cell Function and Interaction
Cytomegalovirus and Herpesvirus Research
HIV Research and Treatment

Notable recent papers by Ted H. Hansen include:

"Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation" (2021, Genome Medicine)
"Neoantigen DNA vaccines are safe, feasible, and induce neoantigen-specific immune responses in triple-negative breast cancer patients" (2024, Genome Medicine)
"Neoantigen DNA vaccines are safe, feasible, and capable of inducing neoantigen-specific immune responses in patients with triple negative breast cancer" (2021, bioRxiv (Cold Spring Harbor Laboratory))
"Metabolomics reveals nucleoside analogs for regulating mucosal-associated invariant T cell responses" (2023, bioRxiv (Cold Spring Harbor Laboratory))

Frequent coauthors who have collaborated with Hansen include:

Lijin Li
Samuel W. Kim
Nancy B. Myers
Mark Sturmoski
Michael D. McLellan

Hansen's publications often appear in the following venues:

Genome Medicine
bioRxiv (Cold Spring Harbor Laboratory)

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

2168
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

1592
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

761
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

625
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

603
Citations
MHC class I antigen presentation: learning from viral evasion strategies

Ted H. Hansen;Marlene Bouvier

534
Citations
MAIT cells are licensed through granzyme exchange to kill bacterially sensitized targets

A Kurioka;J E Ussher;C Cosgrove;C Clough

391
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

380
Citations
Early and nonreversible decrease of CD161++ /MAIT cells in HIV infection.

Cormac Cosgrove;James E. Ussher;Andri Rauch;Kathleen Gärtner

361
Citations
Polyclonal mucosa-associated invariant T cells have unique innate functions in bacterial infection.

Wei-Jen Chua;Steven M. Truscott;Christopher S. Eickhoff;Azra Blazevic

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

302
Citations
Structural insight into MR1-mediated recognition of the mucosal associated invariant T cell receptor

Rangsima Reantragoon;Lars Kjer-Nielsen;Onisha G Patel;Zhenjun Chen

217
Citations
Recognition by CD8 on cytotoxic T lymphocytes is ablated by several substitutions in the class I alpha 3 domain: CD8 and the T-cell receptor recognize the same class I molecule.

Janet M. Connolly;Ted H. Hansen;Amie L. Ingold;Terry A. Potter

216
Citations
MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage

Marielle C. Gold;James E. McLaren;Joseph A. Reistetter;Sue Smyk-Pearson

216
Citations
Alloreactive cytotoxic T lymphocytes generated in the presence of viral- derived peptides show exquisite peptide and MHC specificity

Martha A. Alexander-Miller;Karen Burke;Ulrich H. Koszinowski;Ted H. Hansen

213
Citations
Peptide ligand-induced conformation and surface expression of the Ld class I MHC molecule

Wen-Rong Lie;Nancy B. Myers;John Gorka;Ronald J. Rubocki

213
Citations
Prominence of beta 2-microglobulin, class I heavy chain conformation, and tapasin in the interactions of class I heavy chain with calreticulin and the transporter associated with antigen processing.

Joyce C. Solheim;Michael R. Harris;Cathy S. Kindle;Ted H. Hansen

199
Citations
MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution

Shouxiong Huang;Emmanuel Martin;Sojung Kim;Lawrence Yu

194
Citations
Cutting edge: single-chain trimers of MHC class I molecules form stable structures that potently stimulate antigen-specific T cells and B cells

Yik Y. L. Yu;Nikolai Netuschil;Lonnie Lybarger;Janet M. Connolly

185
Citations
Evidence for MR1 antigen presentation to mucosal-associated invariant T cells

Shouxiong Huang;Susan Gilfillan;Marina Cella;Michael J. Miley

177
Citations