G. ROMA

1.5k total citations
59 papers, 1.4k citations indexed

About

G. ROMA is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, G. ROMA has authored 59 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Organic Chemistry, 22 papers in Pharmacology and 14 papers in Molecular Biology. Recurrent topics in G. ROMA's work include Synthesis of Organic Compounds (22 papers), Synthesis and biological activity (17 papers) and Synthesis of heterocyclic compounds (14 papers). G. ROMA is often cited by papers focused on Synthesis of Organic Compounds (22 papers), Synthesis and biological activity (17 papers) and Synthesis of heterocyclic compounds (14 papers). G. ROMA collaborates with scholars based in Italy. G. ROMA's co-authors include Mario Di Braccio, Giancarlo Grossi, Marco Ghia, Francesca Mattioli, Giuliana Leoncini, Maria Grazia Signorello, Daniela Piras, Massimo Mura, Laura Vargiu and Maria Elena Marongiu and has published in prestigious journals such as Pain, Neuroscience and Journal of Medicinal Chemistry.

In The Last Decade

G. ROMA

58 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
G. ROMA Italy	19	1.2k	344	226	93	57	59	1.4k
Mario Di Braccio Italy	21	1.2k 1.0×	375 1.1×	270 1.2×	94 1.0×	58 1.0×	47	1.5k
Lilian Alcaraz United Kingdom	23	1.0k 0.9×	471 1.4×	214 0.9×	116 1.2×	48 0.8×	44	1.4k
Giancarlo Grossi Italy	22	1.1k 0.9×	390 1.1×	168 0.7×	101 1.1×	57 1.0×	50	1.4k
George C. Rovnyak United States	15	2.1k 1.8×	422 1.2×	249 1.1×	81 0.9×	32 0.6×	26	2.3k
Takashi Inaba Japan	18	539 0.5×	385 1.1×	226 1.0×	93 1.0×	32 0.6×	50	1.1k
Delphine Joseph France	18	946 0.8×	275 0.8×	124 0.5×	134 1.4×	59 1.0×	64	1.3k
Pilar López‐Alvarado Spain	18	732 0.6×	247 0.7×	105 0.5×	74 0.8×	54 0.9×	53	976
Daniel Yohannes United States	25	1.1k 1.0×	805 2.3×	284 1.3×	40 0.4×	50 0.9×	48	1.6k
Masanao Inagaki Japan	14	730 0.6×	152 0.4×	180 0.8×	61 0.7×	40 0.7×	27	1.0k
Hidetsura Cho Japan	16	971 0.8×	376 1.1×	105 0.5×	93 1.0×	24 0.4×	54	1.2k

Countries citing papers authored by G. ROMA

Since Specialization

Citations

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

Fields of papers citing papers by G. ROMA

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. ROMA. 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 G. ROMA. The network helps show where G. ROMA may publish in the future.

Co-authorship network of co-authors of G. ROMA

This figure shows the co-authorship network connecting the top 25 collaborators of G. ROMA. A scholar is included among the top collaborators of G. ROMA 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 G. ROMA. G. ROMA 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

ROMA, G., Mario Di Braccio, Giancarlo Grossi, et al.. (2009). 1,8-Naphthyridines VIII. Novel 5-aminoimidazo[1,2-a] [1,8]naphthyridine-6-carboxamide and 5-amino[1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamide derivatives showing potent analgesic or anti-inflammatory activity, respectively, and completely devoid of acute gastrolesivity. European Journal of Medicinal Chemistry. 45(1). 352–366. 38 indexed citations

ROMA, G., Giancarlo Grossi, Mario Di Braccio, et al.. (2007). 1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity. European Journal of Medicinal Chemistry. 43(8). 1665–1680. 63 indexed citations

Braccio, Mario Di, et al.. (2007). 1,8-Naphthyridines VI. Synthesis and anti-inflammatory activity of 5-(alkylamino)-N,N-diethyl[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides with a new substitution pattern on the triazole ring. European Journal of Medicinal Chemistry. 43(3). 584–594. 31 indexed citations

Dianzani, Chiara, Massimo Collino, Margherita Gallicchio, et al.. (2006). Effects of anti-inflammatory [1, 2, 4]triazolo[4, 3-a] [1, 8]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study. Journal of Inflammation. 3(1). 4–4. 23 indexed citations

Braccio, Mario Di, Giancarlo Grossi, G. ROMA, Maria Grazia Signorello, & Giuliana Leoncini. (2004). Synthesis and in vitro inhibitory activity on human platelet aggregation of novel properly substituted 4-(1-piperazinyl)coumarins. European Journal of Medicinal Chemistry. 39(5). 397–409. 22 indexed citations

Grossi, Giancarlo, Mario Di Braccio, G. ROMA, et al.. (2004). 1,8-Naphthyridines V. Novel N-substituted 5-amino-N,N-diethyl-9-isopropyl [1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, as potent anti-inflammatory and/or analgesic agents completely devoid of acute gastrolesivity. European Journal of Medicinal Chemistry. 40(2). 155–165. 39 indexed citations

Leoncini, Giuliana, et al.. (2003). Mechanisms involved in the antiplatelet activity of 8-methyl-4-(1-piperazinyl)-7-(3-pyridinylmethoxy)-2H-1-benzopyran-2-one (RC414). Biochemical Pharmacology. 67(5). 911–918. 15 indexed citations

Braccio, Mario Di, et al.. (2003). Pyran derivatives. Il Farmaco. 58(11). 1083–1097. 37 indexed citations

Fruscella, Paolo, Marcello Sottocorno, Mario Di Braccio, et al.. (2001). 1,5-Benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandinE2production. Pharmacological Research. 43(5). 445–451. 46 indexed citations

10.

Braccio, Mario Di, Giancarlo Grossi, G. ROMA, et al.. (2001). 1,5-Benzodiazepines. Part XII. Synthesis and biological evaluation of tricyclic and tetracyclic 1,5-benzodiazepine derivatives as nevirapine analogues. European Journal of Medicinal Chemistry. 36(11-12). 935–949. 128 indexed citations

11.

ROMA, G., Mario Di Braccio, Giancarlo Grossi, Francesca Mattioli, & Marco Ghia. (2000). 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities. European Journal of Medicinal Chemistry. 35(11). 1021–1035. 400 indexed citations

12.

ROMA, G., Mario Di Braccio, Giancarlo Grossi, et al.. (2000). Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino-4H-pyrido[1,2-a]pyrimidin-4-ones, their congeners and isosteric analogues. Bioorganic & Medicinal Chemistry. 8(4). 751–768. 35 indexed citations

13.

Carnasciali, Maria Maddalena, et al.. (2000). 8-Chloro-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-5(6H)-one. Acta Crystallographica Section C Crystal Structure Communications. 56(2). 258–259. 1 indexed citations

14.

ROMA, G., et al.. (1998). Pyran derivatives XX. 2-Aminochromone benzo-fused derivatives with antiproliferative properties. Il Farmaco. 53(7). 494–503. 11 indexed citations

15.

Leoncini, Giuliana, Maria Grazia Signorello, G. ROMA, & Mario Di Braccio. (1997). Effect of 2(1-piperazinyl)-4H-pyrido[1,2-a]pyrimidin-4-one (AP155) on human platelets in vitro. Biochemical Pharmacology. 53(11). 1667–1672. 22 indexed citations

16.

Braccio, Mario Di, et al.. (1996). ChemInform Abstract: Pyran Derivatives. Part 19. Dialkylamino‐Substituted 1‐Benzopyranones and Naphthopyranones with Platelet Antiaggregating Activity.. ChemInform. 27(18). 3 indexed citations

17.

ROMA, G., et al.. (1991). 1,5-Benzodiazepines IX. A new route to substituted 4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-5-amines with analgesic and/or anti-inflammatory activities. European Journal of Medicinal Chemistry. 26(5). 489–496. 61 indexed citations

18.

Mazzei, Mauro, et al.. (1988). Formation of 2,6-dimethoxy-1,4-benzoquinone, a highly genotoxic compound, from the reaction of sodium nitrite with the sympathomimetic drug dimethophrine in acidic aqueous solution.. PubMed. 43(6). 523–38. 2 indexed citations

19.

Corli, Oscar, et al.. (1984). Double-blind placebo-controlled trial of baclofen, alone and in combination, in patients undergoing voluntary abortion.. PubMed. 6(6). 800–7. 11 indexed citations

20.

ROMA, G., et al.. (1976). 12H‐naphtho[1′,2′:5,6]pyrano[2,3‐d]pyrimidine derivatives. Journal of Heterocyclic Chemistry. 13(4). 761–764. 5 indexed citations

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