Graham J. Moore

2.2k total citations
115 papers, 1.8k citations indexed

About

Graham J. Moore is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry. According to data from OpenAlex, Graham J. Moore has authored 115 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Molecular Biology, 18 papers in Cellular and Molecular Neuroscience and 14 papers in Organic Chemistry. Recurrent topics in Graham J. Moore's work include Receptor Mechanisms and Signaling (39 papers), Chemical Synthesis and Analysis (29 papers) and Neuropeptides and Animal Physiology (15 papers). Graham J. Moore is often cited by papers focused on Receptor Mechanisms and Signaling (39 papers), Chemical Synthesis and Analysis (29 papers) and Neuropeptides and Animal Physiology (15 papers). Graham J. Moore collaborates with scholars based in Canada, Greece and Australia. Graham J. Moore's co-authors include John Matsoukas, Adebayo Laniyonu, Morley D. Hollenberg, Thomas Mavromoustakos, Robert R. Crichton, Mahmoud Saifeddine, Ikunobu Muramatsu, Peter Jones, David M. Waisman and Konstantinos Kelaidonis and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical Journal and Brain Research.

In The Last Decade

Graham J. Moore

114 papers receiving 1.8k citations

Peers

Graham J. Moore

CMN

HEMAT

CCM

GENET

Alan C. Rigby United States

Thomas E. Hughes United States

Greet Vanhoof Belgium

David B. Glass United States

Chaohong Sun United States

Choel Kim United States

Mauro Zurini Switzerland

Maria L. Webb United States

Daniel Lundell United States

Patrizia Cristofori Italy

Alan C. Rigby United States

Graham J. Moore

1.6k ×1.5

132 ×0.4

CMN

184 ×0.6

HEMAT

70 ×0.3

CCM

81 ×0.4

GENET

Citations per year, relative to Graham J. Moore Graham J. Moore (= 1×) peers Alan C. Rigby

Countries citing papers authored by Graham J. Moore

Since Specialization

Citations

This map shows the geographic impact of Graham J. Moore'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 Graham J. Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Graham J. Moore more than expected).

Fields of papers citing papers by Graham J. Moore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Graham J. Moore. 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 Graham J. Moore. The network helps show where Graham J. Moore may publish in the future.

Co-authorship network of co-authors of Graham J. Moore

This figure shows the co-authorship network connecting the top 25 collaborators of Graham J. Moore. A scholar is included among the top collaborators of Graham J. Moore 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 Graham J. Moore. Graham J. Moore 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

Moore, Graham J., Laura Kate Gadanec, Vasso Apostolopoulos, et al.. (2024). Structural Features Influencing the Bioactive Conformation of Angiotensin II and Angiotensin A: Relationship between Receptor Desensitization, Addiction, and the Blood–Brain Barrier. International Journal of Molecular Sciences. 25(11). 5779–5779. 4 indexed citations

Gadanec, Laura Kate, Vasso Apostolopoulos, Veroniki P. Vidali, et al.. (2023). Existence of Quantum Pharmacology in Sartans: Evidence in Isolated Rabbit Iliac Arteries. International Journal of Molecular Sciences. 24(24). 17559–17559. 3 indexed citations

Kelaidonis, Konstantinos, Massimiliano Peana, Sotirios Tsiodras, et al.. (2023). Network-Based Prediction of Side Effects of Repurposed Antihypertensive Sartans against COVID-19 via Proteome and Drug-Target Interactomes. Proteomes. 11(2). 21–21. 1 indexed citations

Ridgway, Harry, Christos T. Chasapis, Konstantinos Kelaidonis, et al.. (2023). Molecular Epidemiology of SARS-CoV-2: The Dominant Role of Arginine in Mutations and Infectivity. Viruses. 15(2). 309–309. 19 indexed citations

Kelaidonis, Konstantinos, Veroniki P. Vidali, Thomas Mavromoustakos, et al.. (2023). Computational and Enzymatic Studies of Sartans in SARS-CoV-2 Spike RBD-ACE2 Binding: The Role of Tetrazole and Perspectives as Antihypertensive and COVID-19 Therapeutics. International Journal of Molecular Sciences. 24(9). 8454–8454. 9 indexed citations

Matsoukas, John, Laura Kate Gadanec, Anthony Zulli, et al.. (2022). Diminazene Aceturate Reduces Angiotensin II Constriction and Interacts with the Spike Protein of Severe Acute Respiratory Syndrome Coronavirus 2. Biomedicines. 10(7). 1731–1731. 8 indexed citations

Moore, Graham J., Harry Ridgway, Konstantinos Kelaidonis, et al.. (2022). Actions of Novel Angiotensin Receptor Blocking Drugs, Bisartans, Relevant for COVID-19 Therapy: Biased Agonism at Angiotensin Receptors and the Beneficial Effects of Neprilysin in the Renin Angiotensin System. Molecules. 27(15). 4854–4854. 10 indexed citations

Ridgway, Harry, Christos T. Chasapis, Konstantinos Kelaidonis, et al.. (2022). Understanding the Driving Forces That Trigger Mutations in SARS-CoV-2: Mutational Energetics and the Role of Arginine Blockers in COVID-19 Therapy. Viruses. 14(5). 1029–1029. 26 indexed citations

Matsoukas, John, Vasso Apostolopoulos, Anthony Zulli, et al.. (2021). From Angiotensin II to Cyclic Peptides and Angiotensin Receptor Blockers (ARBs): Perspectives of ARBs in COVID-19 Therapy. Molecules. 26(3). 618–618. 12 indexed citations

10.

Tselios, Theodore, Ioanna Daliani, Lesley Probert, et al.. (2000). Treatment of experimental allergic encephalomyelitis (EAE) induced by guinea pig myelin basic protein epitope 72–85 with a Human MBP87–99 analogue and effects of cyclic peptides. Bioorganic & Medicinal Chemistry. 8(8). 1903–1909. 32 indexed citations

11.

Vlahakos, Demetrios, Julian R. Smith, Thomas Mavromoustakos, et al.. (1999). Design and synthesis of thrombin receptor-derived nonpeptide mimetics utilizing a piperazine scaffold. Bioorganic & Medicinal Chemistry. 7(6). 1033–1041. 9 indexed citations

12.

Tselios, Theodore, et al.. (1998). Design and synthesis of small semi-mimetic peptides with immunomodulatory activity based on Myelin Basic Protein (MBP). Amino Acids. 14(4). 333–341. 13 indexed citations

13.

Matsoukas, John, Morley D. Hollenberg, Thomas Mavromoustakos, et al.. (1997). Conformational Analysis of the Thrombin Receptor Agonist Peptides SFLLR and SFLLR-NH2 by NMR: Evidence for a Cyclic Bioactive Conformation. Journal of Protein Chemistry. 16(2). 113–131. 14 indexed citations

14.

Gonzalez, G. C., et al.. (1995). Angiotensinogen-like epitopes are present in the CNS of Aplysia californica and co-localize with urotensin I-and urotensin II-like immunoreactivities in the cerebral ganglia. Neuroreport. 6(3). 541–544. 18 indexed citations

15.

Beck, James P., et al.. (1993). Reciprocal modulation of the binding of angiotensin agonists and antagonists to angiotensin receptors in smooth muscle. General Pharmacology The Vascular System. 24(3). 705–713. 3 indexed citations

16.

Moore, Graham J., et al.. (1993). Influence of methylation of the histidine ring of [Sar¹]angiotensin II on conformation and biological activity. International journal of peptide & protein research. 42(5). 445–449. 4 indexed citations

17.

Matsoukas, John, et al.. (1992). Structure of N-tert-butoxycarbonyl-L-phenylalanine benzyl ester. Acta Crystallographica Section C Crystal Structure Communications. 48(1). 216–217. 1 indexed citations

18.

Hollenberg, Morley D., et al.. (1992). Action of thrombin receptor polypeptide in gastric smooth muscle: identification of a core pentapeptide retaining full thrombin-mimetic intrinsic activity.. Molecular Pharmacology. 42(2). 186–191. 51 indexed citations

19.

Moore, Graham J., et al.. (1991). Importance of the N‐terminal domain of the type I angiotension II antagonist [Sar¹,Ile⁸]ANG II for receptor blockade. International journal of peptide & protein research. 38(1). 1–7. 3 indexed citations

20.

Matsoukas, John, Raghav Yamdagni, & Graham J. Moore. (1990). II. 1H-NMR studies of sarmesin and [des1]sarmesin conformation in dimethylsulfoxide by nuclear Overhauser effect (NOE) enhancement spectroscopy: Folding of the N- and C-terminal domains. Peptides. 11(2). 367–374. 11 indexed citations

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