D. Moura
About
D. Moura is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine.
According to data from OpenAlex, D. Moura has authored 62 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 19 papers in Physiology and 13 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in D. Moura's work include Receptor Mechanisms and Signaling (23 papers), Nitric Oxide and Endothelin Effects (11 papers) and Pharmacological Effects and Assays (8 papers). D. Moura is often cited by papers focused on Receptor Mechanisms and Signaling (23 papers), Nitric Oxide and Endothelin Effects (11 papers) and Pharmacological Effects and Assays (8 papers). D. Moura collaborates with scholars based in Portugal, Germany and Czechia. D. Moura's co-authors include Serafim Guimarães, Sofia Magina, S. Guimarães, M. Q. Paiva, Hélder Pinheiro, Luís Coentrão, Klaus Fink, M. G�thert, Gerhard J. Molderings and Isabel Azevedo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Pharmacological Reviews and Journal of Pharmacology and Experimental Therapeutics.
In The Last Decade
D. Moura
61 papers receiving 1.7k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| D. Moura Portugal | 16 | 695 | 380 | 335 | 329 | 266 | 62 | 1.8k | ||
| Jialie Luo United States | 26 | 779 1.1× | 102 0.3× | 560 1.7× | 363 1.1× | 71 0.3× | 53 | 2.0k | ||
| Yeon Ja Choi South Korea | 27 | 801 1.2× | 435 1.1× | 454 1.4× | 55 0.2× | 50 0.2× | 54 | 2.2k | ||
| Christopher B. Heward United States | 20 | 563 0.8× | 262 0.7× | 265 0.8× | 151 0.5× | 37 0.1× | 27 | 1.8k | ||
| Μάριος Μαρσέλος Greece | 30 | 803 1.2× | 107 0.3× | 203 0.6× | 399 1.2× | 34 0.1× | 120 | 2.8k | ||
| Tadayoshi Takeuchi Japan | 31 | 1.5k 2.2× | 169 0.4× | 756 2.3× | 762 2.3× | 147 0.6× | 140 | 3.0k | ||
| Tomohiro Omura Japan | 26 | 738 1.1× | 411 1.1× | 245 0.7× | 217 0.7× | 55 0.2× | 119 | 2.2k | ||
| Gloria Salazar United States | 31 | 1.5k 2.1× | 810 2.1× | 612 1.8× | 303 0.9× | 143 0.5× | 65 | 2.9k | ||
| Yasuyuki Ishii Japan | 32 | 843 1.2× | 120 0.3× | 262 0.8× | 251 0.8× | 34 0.1× | 90 | 2.5k | ||
| Christopher M. Fanger United States | 15 | 1.6k 2.2× | 160 0.4× | 1.2k 3.4× | 1.1k 3.5× | 213 0.8× | 18 | 3.7k | ||
| Subbiah Pugazhenthi United States | 32 | 1.8k 2.6× | 261 0.7× | 902 2.7× | 422 1.3× | 109 0.4× | 82 | 4.0k |
Countries citing papers authored by D. Moura
Since
Specialization
Citations
This map shows the geographic impact of D. Moura'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 D. Moura with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. Moura more than expected).
Fields of papers citing papers by D. Moura
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by D. Moura. 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 D. Moura. The network helps show where D. Moura may publish in the future.
Co-authorship network of co-authors of D. Moura
This figure shows the co-authorship network connecting the top 25 collaborators of D. Moura. A scholar is included among the top collaborators of D. Moura 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 D. Moura. D. Moura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Pisani, Cristiano, Vera Demarchi Aiello, Idágene A. Cestari, et al.. (2023). Safety of an esophageal deviator for atrial fibrillation catheter ablation. Heart Rhythm O2. 4(9). 565–573.
2.
Rosário, Mateus Santana do, Pedro Antônio Pereira de Jesus, Cleiton Silva Santos, et al.. (2022). Guillain-Barré Syndrome and Miller Fisher Syndrome in Association With an Arboviral Outbreak: A Brazilian Case Series. Frontiers in Medicine. 9. 911175–911175.
3.
Figueira, Luís, Fátima Ferreirinha, Paula Serrão, et al.. (2018). Regulation of corneal noradrenaline release and topography of sympathetic innervation: Functional implications for adrenergic mechanisms in the human cornea. Experimental Eye Research. 174. 121–132.
4.
Lukoyanov, Nikolay, et al.. (2016). Epinephrine increases contextual learning through activation of peripheral β2-adrenoceptors. Psychopharmacology. 233(11). 2099–2108.
5.
Marques, Cláudia, Manuela Amorim, Joana Odila Pereira, et al.. (2015). In vitro ACE-inhibitory peptide KGYGGVSLPEW facilitates noradrenaline release from sympathetic nerve terminals: Relationship with the lack of antihypertensive effect on spontaneous hypertensive rats. Peptides. 71. 72–76.
6.
Coentrão, Luís, et al.. (2010). Hydroxocobalamin treatment of acute cyanide poisoning with a jewellery-cleaning solution: Figure 1. BMJ Case Reports. 2010. bcr0120102603–bcr0120102603.
7.
Morato, Manuela, Dora Pinho, Teresa Sousa, et al.. (2006). Pre- and postjunctional effects of angiotensin II in hypertension due to adenosine receptor blockade. European Journal of Pharmacology. 531(1-3). 209–216.
8.
Queiróz, Glória, et al.. (2006). Involvement of G-protein βγ subunits on the influence of inhibitory α2-autoreceptors on the angiotensin AT1-receptor modulation of noradrenaline release in the rat vas deferens. Neurochemistry International. 49(7). 698–707.
9.
Moura, Eduardo, Paulo Costa, D. Moura, Serafim Guimarães, & Maria Augusta Vieira‐Coelho. (2005). Decreased tyrosine hydroxylase activity in the adrenals of spontaneously hypertensive rats. Life Sciences. 76(25). 2953–2964.
10.
Pinheiro, Hélder, et al.. (2002). A comparison of AT 1 angiotensin II antagonists at pre- and postjunctional angiotensin II receptors of the rat tail artery. Naunyn-Schmiedeberg s Archives of Pharmacology. 366(6). 537–542.
11.
Mota, Alberto, M. Q. Paiva, D. Moura, & S. Guimarães. (2000). Lack of interaction between α2-autoreceptors and prejunctional receptors mediating a facilitatory effect on noradrenaline release. Pharmacological Research. 42(4). 383–387.
12.
Calhau, Conceição, Fátima Martel, D. Moura, & Isabel Azevedo. (2000). SOMATOSTATIN INHIBITS THE RELEASE OF NORADRENALINE INDUCED BY ELECTRICAL STIMULATION OF THE RAT MESENTERIC ARTERY. Pharmacological Research. 41(4). 497–501.
13.
Guimarães, João Tiago, M. Q. Paiva, D. Moura, & S. Guimarães. (1998). Influence of maturation and ageing on the biotransformation of noradrenaline in the rat. Journal of neural transmission. Supplementum. 52. 225–232.
14.
Guimarães, S., Isabel Vitória Figueiredo, Maria Margarida Caramona, D. Moura, & M. Q. Paiva. (1998). Prejunctional α2A-autoreceptors in the human gastric and ileocolic arteries. Naunyn-Schmiedeberg s Archives of Pharmacology. 358(2). 207–211.
15.
Paiva, M. Q., Alberto Mota, D. Moura, & S. Guimarães. (1997). Prejunctional α2A-autoreceptors in the canine saphenous vein. Naunyn-Schmiedeberg s Archives of Pharmacology. 356(3). 368–373.
16.
Vaz‐da‐Silva, Manuel, et al.. (1996). The role of the endocardium in the facilitatory effect of bradykinin on electrically‐induced release of noradrenaline in rat cardiac ventricle. British Journal of Pharmacology. 118(2). 364–368.
17.
Guimarães, S., M. Q. Paiva, D. Moura, Manuel Vaz‐da‐Silva, & António Albino‐Teixeira. (1994). Long-term administration of 1,3-dipropyl-8-sulphophenylxanthine (DPSPX) alters ?2-adrenoceptor-mediated effects at the pre- but not at the postjunctional level. Naunyn-Schmiedeberg s Archives of Pharmacology. 350(6). 692–5.
18.
Moura, D., et al.. (1993). Release and disposition of 3H-noradrenaline in the saphenous vein of neonate and adult dogs. Naunyn-Schmiedeberg s Archives of Pharmacology. 347(2). 186–91.
19.
Pereira, Oduvaldo Câmara Marques, et al.. (1991). Involvement of ?1- and ?2-adrenoceptors in the responses of proximal and distal segments of the canine saphenous vein to exogenous and endogenous noradrenaline. Naunyn-Schmiedeberg s Archives of Pharmacology. 343(6). 616–22.
20.
Moura, D., Manuel Vaz‐da‐Silva, & Serafim Guimarães. (1990). α-Adrenoceptor reserve in the canine cephalic vein. European Journal of Pharmacology. 179(1-2). 9–16.
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.
Explore authors with similar magnitude of impact
Breakdown of academic impact, for papers by Jialie Luo Breakdown of academic impact, for papers by Yeon Ja Choi Breakdown of academic impact, for papers by Christopher B. Heward Breakdown of academic impact, for papers by Μάριος Μαρσέλος Breakdown of academic impact, for papers by Tadayoshi Takeuchi Breakdown of academic impact, for papers by Tomohiro Omura Breakdown of academic impact, for papers by Gloria Salazar Breakdown of academic impact, for papers by Yasuyuki Ishii Breakdown of academic impact, for papers by Christopher M. Fanger Breakdown of academic impact, for papers by Subbiah Pugazhenthi