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
Neuroscience D-index 65 Citations 14,694 130 World Ranking 1815 National Ranking 880

Overview

What is she best known for?

The fields of study she is best known for:

  • Internal medicine
  • Neurotransmitter
  • Pharmacology

Her primary areas of study are Nociception, Pharmacology, Neuropathic pain, Hyperalgesia and Receptor. Nociception is closely attributed to Spinal cord in her study. Her studies in Spinal cord integrate themes in fields like Substance P-Saporin and Astrocyte.

Prisca Honore combines subjects such as Inflammation, Antagonist, TRPV1, Substance P and Dorsal root ganglion with her study of Pharmacology. Her Neuropathic pain study combines topics in areas such as Chronic pain and Allodynia. Her Hyperalgesia research incorporates themes from Anesthesia, Sciatic nerve and Noxious stimulus.

Her most cited work include:

  • Inhibition of hyperalgesia by ablation of lamina I spinal neurons expressing the substance P receptor. (550 citations)
  • Inhibition of hyperalgesia by ablation of lamina I spinal neurons expressing the substance P receptor. (550 citations)
  • Murine models of inflammatory, neuropathic and cancer pain each generates a unique set of neurochemical changes in the spinal cord and sensory neurons. (499 citations)

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

Her main research concerns Pharmacology, Nociception, Spinal cord, Neuropathic pain and Internal medicine. Prisca Honore interconnects Agonist, Receptor, Antagonist, Cannabinoid and TRPV1 in the investigation of issues within Pharmacology. Specifically, her work in Nociception is concerned with the study of Hyperalgesia.

Her Spinal cord research is multidisciplinary, relying on both Central nervous system, Anatomy, Stimulation, Carrageenan and Neurochemical. Her Neuropathic pain research includes elements of Analgesic, Metabotropic receptor and Allodynia. As part of the same scientific family, she usually focuses on Internal medicine, concentrating on Endocrinology and intersecting with -Naloxone and Noxious stimulus.

She most often published in these fields:

  • Pharmacology (48.25%)
  • Nociception (48.25%)
  • Spinal cord (40.56%)

What were the highlights of her more recent work (between 2008-2015)?

  • Pharmacology (48.25%)
  • Neuropathic pain (30.77%)
  • Analgesic (21.68%)

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

Prisca Honore spends much of her time researching Pharmacology, Neuropathic pain, Analgesic, Nociception and Anesthesia. Her Pharmacology study integrates concerns from other disciplines, such as Agonist, Antagonist, Cannabinoid, Receptor and Allosteric regulation. Her Neuropathic pain research is multidisciplinary, incorporating elements of Internal medicine, Stereochemistry and Endocrinology.

Her work investigates the relationship between Nociception and topics such as Oral administration that intersect with problems in Blockade, ED50 and P2 receptor. Her Anesthesia study incorporates themes from Celecoxib, Stimulation, Peripheral and Chronic pain. The various areas that Prisca Honore examines in her Cannabinoid receptor study include Neuroscience, Spinal cord and Opioid peptide.

Between 2008 and 2015, her most popular works were:

  • Repeated dosing of ABT-102, a potent and selective TRPV1 antagonist, enhances TRPV1-mediated analgesic activity in rodents, but attenuates antagonist-induced hyperthermia (110 citations)
  • Pharmacological modulation of movement-evoked pain in a rat model of osteoarthritis. (101 citations)
  • Central and peripheral sites of action for CB2 receptor mediated analgesic activity in chronic inflammatory and neuropathic pain models in rats (88 citations)

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

  • Internal medicine
  • Neurotransmitter
  • Agonist

Her primary areas of investigation include Pharmacology, Analgesic, Neuropathic pain, Antagonist and Receptor. The study incorporates disciplines such as Celecoxib, Acetaminophen and Knee Joint in addition to Analgesic. Her research investigates the connection between Neuropathic pain and topics such as Cannabinoid receptor type 2 that intersect with problems in Opioid peptide, Neuralgia, Neuroscience and Spinal cord.

She has researched Antagonist in several fields, including Endocrinology and Nociception. Her Nociception research is multidisciplinary, incorporating elements of Capsaicin, TRPV1, Transient receptor potential channel, Hyperthermia and Threshold of pain. Her Receptor research is multidisciplinary, incorporating perspectives in Cytokine, Immunology and Systemic administration.

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

Inhibition of hyperalgesia by ablation of lamina I spinal neurons expressing the substance P receptor.

Patrick W. Mantyh;Scott D. Rogers;Scott D. Rogers;Prisca Honore;Prisca Honore;Brian J. Allen;Brian J. Allen.
Science (1997)

699 Citations

Neurochemical and cellular reorganization of the spinal cord in a murine model of bone cancer pain

Matthew J. Schwei;Prisca Honore;Scott D. Rogers;Janeen L. Salak-Johnson.
The Journal of Neuroscience (1999)

681 Citations

Murine models of inflammatory, neuropathic and cancer pain each generates a unique set of neurochemical changes in the spinal cord and sensory neurons.

P Honore;S.D Rogers;M.J Schwei;J.L Salak-Johnson.
Neuroscience (2000)

661 Citations

Osteoprotegerin blocks bone cancer-induced skeletal destruction, skeletal pain and pain-related neurochemical reorganization of the spinal cord

Prisca Honore;Nancy M. Luger;Nancy M. Luger;Mary Ann C. Sabino;Mary Ann C. Sabino;Matthew J. Schwei;Matthew J. Schwei.
Nature Medicine (2000)

596 Citations

A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat

Michael F. Jarvis;Prisca Honore;Char Chang Shieh;Mark Chapman.
Proceedings of the National Academy of Sciences of the United States of America (2007)

543 Citations

A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat

Michael F. Jarvis;Edward C. Burgard;Steve McGaraughty;Prisca Honore.
Proceedings of the National Academy of Sciences of the United States of America (2002)

528 Citations

A-740003 [N-(1-{[(Cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a Novel and Selective P2X7 Receptor Antagonist, Dose-Dependently Reduces Neuropathic Pain in the Rat

Prisca Honore;Diana Donnelly-Roberts;Marian T. Namovic;Gin Hsieh.
Journal of Pharmacology and Experimental Therapeutics (2006)

522 Citations

Transmission of chronic nociception by spinal neurons expressing the substance P receptor.

Michael L. Nichols;Michael L. Nichols;Brian J. Allen;Brian J. Allen;Scott D. Rogers;Scott D. Rogers;Joseph R. Ghilardi;Joseph R. Ghilardi.
Science (1999)

505 Citations

A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel Transient Receptor Potential Type V1 Receptor Antagonist, Relieves Pathophysiological Pain Associated with Inflammation and Tissue Injury in Rats

Prisca Honore;Carol T Wismer;Joseph P Mikusa;Chang Z Zhu.
Journal of Pharmacology and Experimental Therapeutics (2005)

366 Citations

TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists

M. Cui;P. Honore;C. Zhong;D. Gauvin.
The Journal of Neuroscience (2006)

361 Citations

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