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
Medicine D-index 120 Citations 64,436 282 World Ranking 2075 National Ranking 1200
Biology and Biochemistry D-index 121 Citations 64,696 279 World Ranking 397 National Ranking 276

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Internal medicine

David M. Stern mainly investigates Cell biology, Receptor, Glycation, RAGE and Internal medicine. David M. Stern has included themes like Endothelial stem cell, Biochemistry, Cell adhesion, Cell surface receptor and Endothelium in his Cell biology study. The study incorporates disciplines such as Inflammation, Proinflammatory cytokine, Immunology and Downregulation and upregulation in addition to Receptor.

His Glycation study integrates concerns from other disciplines, such as Amyloid beta, Intracellular signal transduction, Regulation of gene expression, Neuroscience and Amyloidosis. His RAGE research includes themes of Signal transduction, Kinase and p38 mitogen-activated protein kinases. His Internal medicine research is multidisciplinary, incorporating elements of Diabetes mellitus and Endocrinology.

His most cited work include:

  • Endothelial Cells in Physiology and in the Pathophysiology of Vascular Disorders (2026 citations)
  • RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides. (1596 citations)
  • Enhanced cellular oxidant stress by the interaction of advanced glycation end products with their receptors/binding proteins. (1179 citations)

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

His primary areas of study are Internal medicine, Cell biology, Endocrinology, Receptor and Immunology. As a part of the same scientific study, he usually deals with the Internal medicine, concentrating on Diabetes mellitus and frequently concerns with Bioinformatics. The concepts of his Cell biology study are interwoven with issues in Endothelial stem cell, Cell, Endothelium and Downregulation and upregulation.

His research in Endocrinology intersects with topics in Proinflammatory cytokine and Pathogenesis. His research on Receptor concerns the broader Biochemistry. His work carried out in the field of Immunology brings together such families of science as Cancer research and Ischemia.

He most often published in these fields:

  • Internal medicine (28.09%)
  • Cell biology (26.42%)
  • Endocrinology (25.08%)

What were the highlights of his more recent work (between 2004-2016)?

  • Internal medicine (28.09%)
  • Endocrinology (25.08%)
  • Biochemistry (18.73%)

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

Internal medicine, Endocrinology, Biochemistry, Cell biology and Glycation are his primary areas of study. His research integrates issues of Diabetes mellitus and Cardiology in his study of Internal medicine. His study in Endocrinology is interdisciplinary in nature, drawing from both Angiotensin II, Bone marrow and Phosphorylation.

The various areas that David M. Stern examines in his Cell biology study include Endothelial stem cell, Adult stem cell, Genetically modified mouse and Amyloid precursor protein. His Glycation study necessitates a more in-depth grasp of Receptor. His biological study spans a wide range of topics, including Inflammation, Cancer research and Kinase.

Between 2004 and 2016, his most popular works were:

  • Mitochondrial Aβ: a potential focal point for neuronal metabolic dysfunction in Alzheimer’s disease (571 citations)
  • The N-terminal domain of thrombomodulin sequesters high-mobility group-B1 protein, a novel antiinflammatory mechanism (450 citations)
  • Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegans. (221 citations)

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

  • Gene
  • Enzyme
  • Internal medicine

Cell biology, Immunology, Neuroscience, Mitochondrion and RAGE are his primary areas of study. His Cell biology research is multidisciplinary, incorporating perspectives in Cell surface receptor, Protein A and Amyloid precursor protein. His Neuroscience research incorporates themes from Receptor and Cerebral organoid.

Endocrinology and Internal medicine are the main areas of his RAGE studies. His Internal medicine study incorporates themes from Unfolded protein response and Pathology. David M. Stern is interested in Glycation, which is a field of Biochemistry.

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

Endothelial Cells in Physiology and in the Pathophysiology of Vascular Disorders

Douglas B. Cines;Eleanor S. Pollak;Clayton A. Buck;Joseph Loscalzo.
Blood (1998)

3507 Citations

RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides.

Marion A Hofmann;Steven Drury;Caifeng Fu;Wu Qu.
Cell (1999)

2207 Citations

Enhanced cellular oxidant stress by the interaction of advanced glycation end products with their receptors/binding proteins.

Shi Du Yan;A. M. Schmidt;G. M. Anderson;Jinghua Zhang.
Journal of Biological Chemistry (1994)

1988 Citations

Modulation of endothelial cell hemostatic properties by tumor necrosis factor.

Peter P. Nawroth;David M. Stern.
Journal of Experimental Medicine (1986)

1896 Citations

The Receptor for Advanced Glycation End Products (RAGE) Is a Cellular Binding Site for Amphoterin MEDIATION OF NEURITE OUTGROWTH AND CO-EXPRESSION OF RAGE AND AMPHOTERIN IN THE DEVELOPING NERVOUS SYSTEM

Osamu Hori;Jerold Brett;Timothy Slattery;Rong Cao.
Journal of Biological Chemistry (1995)

1645 Citations

The multiligand receptor RAGE as a progression factor amplifying immune and inflammatory responses

Ann Marie Schmidt;Shirley ShiDu Yan;Shi Fang Yan;David M. Stern.
Journal of Clinical Investigation (2001)

1635 Citations

Blockade of RAGE–amphoterin signalling suppresses tumour growth and metastases

Taguchi A;Blood Dc;del Toro G;Canet A.
Nature (2000)

1572 Citations

RAGE mediates amyloid-beta peptide transport across the blood-brain barrier and accumulation in brain.

Rashid Deane;Shi Du Yan;Ram Kumar Submamaryan;Barbara LaRue.
Nature Medicine (2003)

1532 Citations

Suppression of accelerated diabetic atherosclerosis by the soluble receptor for advanced glycation endproducts.

Lisa Park;Kathleen G. Raman;Kenneth J. Lee;Yan Lu.
Nature Medicine (1998)

1372 Citations

Activation of NADPH oxidase by AGE links oxidant stress to altered gene expression via RAGE.

Marie-Paule Wautier;Olivier Chappey;Stefano Corda;David M. Stern.
American Journal of Physiology-endocrinology and Metabolism (2001)

1337 Citations

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