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 115 Citations 41,225 484 World Ranking 237 National Ranking 157
Medicine D-index 118 Citations 44,278 567 World Ranking 2312 National Ranking 1344

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Immune system
  • Internal medicine

Wayne W. Hancock spends much of his time researching Immunology, Transplantation, T cell, Chemokine and Immune system. His study in Chemokine receptor, Cytokine, Proinflammatory cytokine, FOXP3 and Immune tolerance falls under the purview of Immunology. His Transplantation research is multidisciplinary, incorporating perspectives in Proteinuria, Ischemia and Pathology.

Wayne W. Hancock combines subjects such as Blockade, CD154, Monoclonal antibody and Antigen with his study of T cell. His Chemokine research incorporates themes from Transplant rejection and Monocyte. Wayne W. Hancock has included themes like Cell adhesion molecule and In vivo in his Immune system study.

His most cited work include:

  • Fibrinogen Stimulates Macrophage Chemokine Secretion Through Toll-Like Receptor 4 (795 citations)
  • Fibrinogen Stimulates Macrophage Chemokine Secretion Through Toll-Like Receptor 4 (795 citations)
  • CCR5(+) and CXCR3(+) T cells are increased in multiple sclerosis and their ligands MIP-1alpha and IP-10 are expressed in demyelinating brain lesions. (776 citations)

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

His primary areas of study are Immunology, Transplantation, Cancer research, FOXP3 and Immune system. His is doing research in T cell, Cytokine, Monoclonal antibody, Antibody and Antigen, both of which are found in Immunology. Monoclonal antibody and Molecular biology are commonly linked in his work.

His Transplantation study combines topics from a wide range of disciplines, such as Immunosuppression, Kidney, Pharmacology and Pathology. His study in FOXP3 is interdisciplinary in nature, drawing from both Transcription factor, Cell biology, Regulatory T cell, Histone and Autoimmunity. His work focuses on many connections between Immune system and other disciplines, such as In vivo, that overlap with his field of interest in In vitro.

He most often published in these fields:

  • Immunology (58.19%)
  • Transplantation (28.93%)
  • Cancer research (20.07%)

What were the highlights of his more recent work (between 2014-2021)?

  • FOXP3 (20.40%)
  • Cancer research (20.07%)
  • Immunology (58.19%)

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

His primary scientific interests are in FOXP3, Cancer research, Immunology, Immune system and T cell. His FOXP3 research integrates issues from Tumor microenvironment, Transcription factor, Cancer immunotherapy, Cell biology and Histone. His work deals with themes such as Chemokine, Vascularized Composite Allotransplantation, Transplantation, Monoclonal antibody and Effector, which intersect with Cancer research.

The concepts of his Immunology study are interwoven with issues in Phenotype and Cancer. He studied Immune system and In vivo that intersect with Mechanism of action. His research integrates issues of Cancer cell, Macrophage and Immune tolerance, Antigen in his study of T cell.

Between 2014 and 2021, his most popular works were:

  • Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments (299 citations)
  • Origin and Role of a Subset of Tumor-Associated Neutrophils with Antigen-Presenting Cell Features in Early-Stage Human Lung Cancer (155 citations)
  • Origin and Role of a Subset of Tumor-Associated Neutrophils with Antigen-Presenting Cell Features in Early-Stage Human Lung Cancer (155 citations)

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

  • Gene
  • Internal medicine
  • Immune system

Wayne W. Hancock mostly deals with FOXP3, Immunology, Cancer research, Histone and Cell biology. His FOXP3 study which covers Transcription factor that intersects with Phosphorylation. His Immunology research is multidisciplinary, incorporating elements of Phenotype and In vitro.

His Cancer research study incorporates themes from Cell and Regulatory T cell, T cell, IL-2 receptor, Immune system. In his study, which falls under the umbrella issue of IL-2 receptor, Transplantation is strongly linked to HDAC11. His Cell biology research includes themes of Tumor microenvironment, Ubiquitin and Immune tolerance.

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

Fibrinogen Stimulates Macrophage Chemokine Secretion Through Toll-Like Receptor 4

Stephen T. Smiley;Jennifer A. King;Wayne W. Hancock;Wayne W. Hancock.
Journal of Immunology (2001)

1165 Citations

Oral tolerance to myelin basic protein and natural recovery from experimental autoimmune encephalomyelitis are associated with downregulation of inflammatory cytokines and differential upregulation of transforming growth factor beta, interleukin 4, and prostaglandin E expression in the brain.

S J Khoury;W W Hancock;H L Weiner.
Journal of Experimental Medicine (1992)

1043 Citations

CCR5+ and CXCR3+ T cells are increased in multiple sclerosis and their ligands MIP-1α and IP-10 are expressed in demyelinating brain lesions

Konstantin E. Balashov;James B. Rottman;Howard L. Weiner;Wayne W. Hancock.
Proceedings of the National Academy of Sciences of the United States of America (1999)

1011 Citations

Deacetylase inhibition promotes the generation and function of regulatory T cells

Ran Tao;Edwin F de Zoeten;Engin Özkaynak;Chunxia Chen.
Nature Medicine (2007)

908 Citations

Requirement of the Chemokine Receptor CXCR3 for Acute Allograft Rejection

Wayne W. Hancock;Bao Lu;Wei Gao;Vilmos Csizmadia.
Journal of Experimental Medicine (2000)

755 Citations

Requirement for T-cell apoptosis in the induction of peripheral transplantation tolerance.

Andrew D. Wells;Xian Chang Li;Yongsheng Li;Matthew C. Walsh.
Nature Medicine (1999)

702 Citations

CD28-B7 blockade after alloantigenic challenge in vivo inhibits Th1 cytokines but spares Th2.

Mohamed H. Sayegh;Enver Akalin;Wayne W. Hancock;Mary E. Russell.
Journal of Experimental Medicine (1995)

666 Citations

Messenger RNA for FOXP3 in the Urine of Renal-Allograft Recipients

Thangamani Muthukumar;Darshana Dadhania;Ruchuang Ding;Catherine Snopkowski.
The New England Journal of Medicine (2005)

622 Citations

Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments

Alessia Angelin;Luis Gil-de-Gómez;Satinder Dahiya;Jing Jiao.
Cell Metabolism (2017)

587 Citations

Antibody-induced transplant arteriosclerosis is prevented by graft expression of anti-oxidant and anti-apoptotic genes.

Wayne W. Hancock;Roland Buelow;Mohamed H. Sayegh;Laurence A. Turka.
Nature Medicine (1998)

562 Citations

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