Joseph Foss

4.1k total citations
70 papers, 3.0k citations indexed

About

Joseph Foss is a scholar working on Surgery, Physiology and Anesthesiology and Pain Medicine. According to data from OpenAlex, Joseph Foss has authored 70 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Surgery, 18 papers in Physiology and 17 papers in Anesthesiology and Pain Medicine. Recurrent topics in Joseph Foss's work include Anesthesia and Pain Management (16 papers), Cardiac, Anesthesia and Surgical Outcomes (15 papers) and Gastrointestinal motility and disorders (10 papers). Joseph Foss is often cited by papers focused on Anesthesia and Pain Management (16 papers), Cardiac, Anesthesia and Surgical Outcomes (15 papers) and Gastrointestinal motility and disorders (10 papers). Joseph Foss collaborates with scholars based in United States, India and Canada. Joseph Foss's co-authors include Michael F. Roizen, Chun‐Su Yuan, Michael O’Connor, Jonathan Moss, Joachim Osinski, Srinivas Mantha, Ronald A. Thisted, Mohamed Naguib, Bihua Bie and Jiang Wu and has published in prestigious journals such as JAMA, SHILAP Revista de lepidopterología and Pain.

In The Last Decade

Joseph Foss

66 papers receiving 2.8k citations

Peers

Joseph Foss

SURGE

GASTR

APM

PHYSI

CCM

W.S. Nimmo United Kingdom

Anne Estrup Olesen Denmark

Søren Schou Olesen Denmark

Kahoru Nishina Japan

Jayne Edwards United Kingdom

David J. Rowbotham United Kingdom

Hidefumi Obara Japan

Katsuya Mikawa Japan

Andrew Moore United Kingdom

Flaminia Coluzzi Italy

W.S. Nimmo United Kingdom

Joseph Foss

1.2k ×0.9

SURGE

357 ×0.5

GASTR

1.5k ×2.4

APM

606 ×1.1

PHYSI

566 ×1.1

CCM

Citations per year, relative to Joseph Foss Joseph Foss (= 1×) peers W.S. Nimmo

Countries citing papers authored by Joseph Foss

Since Specialization

Citations

This map shows the geographic impact of Joseph Foss's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Joseph Foss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joseph Foss more than expected).

Fields of papers citing papers by Joseph Foss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph Foss. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Joseph Foss. The network helps show where Joseph Foss may publish in the future.

Co-authorship network of co-authors of Joseph Foss

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph Foss. A scholar is included among the top collaborators of Joseph Foss based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Joseph Foss. Joseph Foss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Johnson, Ken B., N. Lynn Henry, Mei Wei, et al.. (2023). Genetic variations that influence paclitaxel pharmacokinetics and intracellular effects that may contribute to chemotherapy-induced neuropathy: A narrative review. SHILAP Revista de lepidopterología. 4. 1139883–1139883. 4 indexed citations

Johnson, Ken B., Bihua Bie, Jennifer Hockings, et al.. (2022). A Multimodal Approach to Discover Biomarkers for Taxane-Induced Peripheral Neuropathy (TIPN): A Study Protocol. Technology in Cancer Research & Treatment. 21. 2213869057–2213869057. 7 indexed citations

Bie, Bihua, Jiang Wu, Joseph Foss, & Mohamed Naguib. (2019). Activation of mGluR1 Mediates C1q-Dependent Microglial Phagocytosis of Glutamatergic Synapses in Alzheimer’s Rodent Models. Molecular Neurobiology. 56(8). 5568–5585. 53 indexed citations

Wu, Jiang, et al.. (2018). Cannabinoid Type 2 Receptor System Modulates Paclitaxel-Induced Microglial Dysregulation and Central Sensitization in Rats. Journal of Pain. 20(5). 501–514. 58 indexed citations

Wu, Jiang, et al.. (2017). Activation of CB2 receptor system restores cognitive capacity and hippocampal Sox2 expression in a transgenic mouse model of Alzheimer's disease. European Journal of Pharmacology. 811. 12–20. 58 indexed citations

Ootaki, Chiyo, Tyler Stevens, John J. Vargo, et al.. (2012). Does General Anesthesia Increase the Diagnostic Yield of Endoscopic Ultrasound-guided Fine Needle Aspiration of Pancreatic Masses?. Anesthesiology. 117(5). 1044–1050. 25 indexed citations

Finnegan, Patrick Sean, et al.. (2012). Use of the CTrach Laryngeal Mask Airway in adult patients: a retrospective review of 126 cases. Journal of Clinical Anesthesia. 24(5). 370–372. 4 indexed citations

Schmith, Virginia D. & Joseph Foss. (2010). Inflammation: Planning for a Source of Pharmacokinetic/Pharmacodynamic Variability in Translational Studies. Clinical Pharmacology & Therapeutics. 87(4). 488–491. 18 indexed citations

Smith, Michael P., et al.. (2008). High-throughput Operating Room System for Joint Arthroplasties Durably Outperforms Routine Processes. Anesthesiology. 109(1). 25–35. 57 indexed citations

10.

Foss, Joseph, et al.. (2008). Effects of Inflammation on Pharmacokinetics/Pharmacodynamics: Increasing Recognition of Its Contribution to Variability in Response. Clinical Pharmacology & Therapeutics. 83(6). 809–811. 37 indexed citations

11.

Camilleri, Michael, Irene Ferber, Duane D. Burton, et al.. (2005). Effect of Alvimopan and Codeine on Gastrointestinal Transit: A Randomized Controlled Study. Clinical Gastroenterology and Hepatology. 3(8). 784–791. 104 indexed citations

12.

Osinski, Joachim, Anbao Wang, Ji An Wu, Joseph Foss, & Chun‐Su Yuan. (2002). Determination of methylnaltrexone in clinical samples by solid-phase extraction and high-performance liquid chromatography for a pharmacokinetics study. Journal of Chromatography B. 780(2). 251–259. 10 indexed citations

13.

Murphy, Damian B., et al.. (2001). Pharmacokinetic profile of epidurally administered methylnaltrexone, a novel peripheral opioid antagonist in a rabbit model. British Journal of Anaesthesia. 86(1). 120–122. 3 indexed citations

14.

Doenicke, Α., et al.. (1999). Reducing Myoclonus after Etomidate . Anesthesiology. 90(1). 113–119. 155 indexed citations

15.

Yuan, Chun‐Su, Joseph Foss, Michael O’Connor, Jonathan Moss, & Michael F. Roizen. (1998). Gut Motility and Transit Changes in Patients Receiving Long‐Term Methadone Maintenance. The Journal of Clinical Pharmacology. 38(10). 931–935. 42 indexed citations

16.

Yuan, Chun‐Su, Joseph Foss, Michael O’Connor, et al.. (1998). Efficacy of orally administered methylnaltrexone in decreasing subjective effects after intravenous morphine. Drug and Alcohol Dependence. 52(2). 161–165. 57 indexed citations

17.

Yuan, Chun‐Su, Joseph Foss, Michael O’Connor, Michael F. Roizen, & Jonathan Moss. (1998). Effects of Low‐Dose Morphine on Gastric Emptying in Healthy Volunteers. The Journal of Clinical Pharmacology. 38(11). 1017–1020. 70 indexed citations

18.

Yuan, Chun‐Su, Joseph Foss, Michael O’Connor, et al.. (1996). Methylnaltrexone prevents morphine-induced delay in oral-cecal transit time without affecting analgesia: A double-blind randomized placebo-controlled trial*. Clinical Pharmacology & Therapeutics. 59(4). 469–475. 159 indexed citations

19.

Amin, Hesham M., et al.. (1994). Efficacy of Methylnaltrexone Versus Naloxone for Reversal of Morphine-Induced Depression of Hypoxic Ventilatory Response. Anesthesia & Analgesia. 78(4). 701???705–701???705. 26 indexed citations

20.

Helsingen, N, et al.. (1980). Tinidazole and Doxycycline as Antimicrobials in Elective Colorectal Surgery: A Randomized Multicentre Trial. Scandinavian Journal of Gastroenterology. 15(sup59). 29–35. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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