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 55 Citations 7,948 184 World Ranking 10718 National Ranking 4635

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Cancer
  • Internal medicine

His primary areas of study are Molecular biology, Fanconi anemia, Haematopoiesis, Immunology and Cell biology. The various areas that Grover C. Bagby examines in his Molecular biology study include Tumor necrosis factor alpha, Interleukin and Regulation of gene expression, Gene. His Fanconi anemia research focuses on Cell culture and how it connects with Cancer research.

The Haematopoiesis study combines topics in areas such as Preleukemia, Dysplasia and Interferon gamma. His biological study spans a wide range of topics, including Neutropenia and Acquired immunodeficiency syndrome. His Cytokine research is multidisciplinary, relying on both Proinflammatory cytokine and Progenitor cell.

His most cited work include:

  • Interleukin 1 stimulates granulocyte macrophage colony-stimulating activity release by vascular endothelial cells. (245 citations)
  • The influence of human immunodeficiency virus-1 on hematopoiesis (239 citations)
  • The preleukemic syndrome (hemopoietic dysplasia). (166 citations)

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

Grover C. Bagby mainly investigates Fanconi anemia, Immunology, Cancer research, Haematopoiesis and Molecular biology. His work deals with themes such as Bone marrow failure and Stem cell, Cell biology, which intersect with Fanconi anemia. His studies deal with areas such as CD34 and Cell cycle as well as Immunology.

His Cancer research research integrates issues from Mitomycin C, Apoptosis, Ovarian cancer and Interferon gamma. His Haematopoiesis research incorporates themes from Endothelial stem cell, In vitro, Gene expression, Progenitor cell and Dysplasia. His Molecular biology research is multidisciplinary, incorporating perspectives in Interleukin, Cell culture, Colony-stimulating factor and Interferon.

He most often published in these fields:

  • Fanconi anemia (56.28%)
  • Immunology (44.72%)
  • Cancer research (43.22%)

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

  • Immunology (44.72%)
  • Cytokine (25.63%)
  • Fanconi anemia (56.28%)

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

His primary areas of study are Immunology, Cytokine, Fanconi anemia, Tumor necrosis factor alpha and Cancer research. His studies examine the connections between Immunology and genetics, as well as such issues in CD34, with regards to Cord blood. His Fanconi anemia study combines topics from a wide range of disciplines, such as Progenitor cell, Stem cell, Cell biology and Ubiquitin ligase.

His study in Progenitor cell is interdisciplinary in nature, drawing from both Haematopoiesis and Hematopoietic stem cell. Grover C. Bagby interconnects Molecular biology, FANCD2, Apoptosis and Peptide in the investigation of issues within Cell biology. His Cancer research research is multidisciplinary, incorporating elements of Caspase 10, Caspase 8, Caspase 3 and Hematopoietic progenitor cells.

Between 2010 and 2021, his most popular works were:

  • TNFα facilitates clonal expansion of JAK2V617F positive cells in myeloproliferative neoplasms (160 citations)
  • Identification of Interleukin-1 by Functional Screening as a Key Mediator of Cellular Expansion and Disease Progression in Acute Myeloid Leukemia (82 citations)
  • TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia (72 citations)

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

  • Gene
  • Cancer
  • Internal medicine

His main research concerns Fanconi anemia, Progenitor cell, Cytokine, Tumor necrosis factor alpha and Haematopoiesis. He has included themes like Bone marrow failure, Cancer research, Stem cell and DNA damage in his Fanconi anemia study. The study incorporates disciplines such as Molecular biology, Hematopoietic stem cell and Bone marrow in addition to Progenitor cell.

The study of Molecular biology is intertwined with the study of Cell biology in a number of ways. His Cytokine research is included under the broader classification of Immunology. His work investigates the relationship between Haematopoiesis and topics such as FANCA that intersect with problems in MAPK/ERK pathway, TLR7 and Reporter gene.

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

Interleukin 1 stimulates granulocyte macrophage colony-stimulating activity release by vascular endothelial cells.

Grover C. Bagby;Charles A. Dinarello;Paul Wallace;Cynthia Wagner.
Journal of Clinical Investigation (1986)

375 Citations

The influence of human immunodeficiency virus-1 on hematopoiesis

Ashlee Moses;Jay Nelson;Grover C. Bagby.
Blood (1998)

364 Citations

The preleukemic syndrome (hemopoietic dysplasia).

James W. Linman;Grover C. Bagby.
Cancer (1978)

252 Citations

Inactivation of the Fanconi Anemia Group C Gene Augments Interferon-γ–Induced Apoptotic Responses in Hematopoietic Cells

R. Keaney Rathbun;R. Keaney Rathbun;Gregory R. Faulkner;Gregory R. Faulkner;Marika H. Ostroski;Marika H. Ostroski;Tracy A. Christianson;Tracy A. Christianson.
Blood (1997)

240 Citations

Genetic basis of Fanconi anemia.

Grover C. Bagby.
Current Opinion in Hematology (2003)

227 Citations

Human immunodeficiency virus infection of bone marrow endothelium reduces induction of stromal hematopoietic growth factors

AV Moses;S Williams;ML Heneveld;J Strussenberg.
Blood (1996)

207 Citations

Hypoxia-induced Nucleophosmin Protects Cell Death through Inhibition of p53

June Li;Xiaoling Zhang;Daniel P. Sejas;Grover C. Bagby.
Journal of Biological Chemistry (2004)

202 Citations

TNFα facilitates clonal expansion of JAK2V617F positive cells in myeloproliferative neoplasms

Angela G. Fleischman;Karl J. Aichberger;Karl J. Aichberger;Samuel B. Luty;Thomas G. Bumm.
Blood (2011)

190 Citations

FANCC interacts with Hsp70 to protect hematopoietic cells from IFN‐γ/TNF‐α‐mediated cytotoxicity

Qishen Pang;Qishen Pang;Winifred Keeble;Tracy A. Christianson;Gregory R. Faulkner.
The EMBO Journal (2001)

185 Citations

The Fanconi anemia protein FANCC binds to and facilitates the activation of STAT1 by gamma interferon and hematopoietic growth factors.

Qishen Pang;Qishen Pang;Sara Fagerlie;Tracy A. Christianson;Winifred Keeble.
Molecular and Cellular Biology (2000)

180 Citations

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