Marija Prhavc

1.4k total citations
30 papers, 798 citations indexed

About

Marija Prhavc is a scholar working on Organic Chemistry, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Marija Prhavc has authored 30 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 12 papers in Molecular Biology and 11 papers in Infectious Diseases. Recurrent topics in Marija Prhavc's work include HIV/AIDS drug development and treatment (10 papers), DNA and Nucleic Acid Chemistry (8 papers) and Synthesis and Characterization of Heterocyclic Compounds (7 papers). Marija Prhavc is often cited by papers focused on HIV/AIDS drug development and treatment (10 papers), DNA and Nucleic Acid Chemistry (8 papers) and Synthesis and Characterization of Heterocyclic Compounds (7 papers). Marija Prhavc collaborates with scholars based in United States, Slovenia and Canada. Marija Prhavc's co-authors include P. Dan Cook, Thazha P. Prakash, Joanne E. Tomassini, Steven S. Carroll, Balkrishen Bhat, David B. Olsen, Anne B. Eldrup, Malcolm MacCoss, Michele Bosserman and Guangyi Wang and has published in prestigious journals such as Journal of the American Chemical Society, PLoS ONE and Journal of Medicinal Chemistry.

In The Last Decade

Marija Prhavc

28 papers receiving 751 citations

Peers

Marija Prhavc
Anne B. Eldrup United States
Stefania Lostia United States
Tony Whitaker United States
Junxing Shi United States
Phillip M. Tharnish United States
Natalia Dyatkina Russia
Michele Bosserman United States
Tamara R. McBrayer United States
Maryam Ehteshami United States
John H. Merrett United Kingdom
Anne B. Eldrup United States
Marija Prhavc
Citations per year, relative to Marija Prhavc Marija Prhavc (= 1×) peers Anne B. Eldrup

Countries citing papers authored by Marija Prhavc

Since Specialization
Citations

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

Fields of papers citing papers by Marija Prhavc

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marija Prhavc

This figure shows the co-authorship network connecting the top 25 collaborators of Marija Prhavc. A scholar is included among the top collaborators of Marija Prhavc 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 Marija Prhavc. Marija Prhavc is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dyatkina, Natalia, Hong Liu, April Kinkade, et al.. (2022). Synthesis and Anti-Hepatitis B Activities of 3′-Fluoro-2′-Substituted Apionucleosides. Molecules. 27(8). 2413–2413. 1 indexed citations
2.
Deval, Jérôme, Amy Fung, Sarah Stevens, et al.. (2016). Biochemical Effect of Resistance Mutations against Synergistic Inhibitors of RSV RNA Polymerase. PLoS ONE. 11(5). e0154097–e0154097. 27 indexed citations
3.
Wang, Guangyi, Jinqiao Wan, X. Wu, et al.. (2016). Synthesis and Anti-Influenza Activity of Pyridine, Pyridazine, and Pyrimidine C-Nucleosides as Favipiravir (T-705) Analogues. Journal of Medicinal Chemistry. 59(10). 4611–4624. 69 indexed citations
4.
Tan, Hua, Kenneth J. Shaw, Jérôme Deval, et al.. (2015). P0682 : Preclinical characterization of AL-335, a potent uridine based nucleoside polymerase inhibitor for the treatment of chronic hepatitis C. Journal of Hepatology. 62. S577–S578. 3 indexed citations
5.
Prhavc, Marija, Natalia Dyatkina, Samantha Koo-McCoy, et al.. (2008). Synthesis and Biological Activity of 7-Deaza-7-ethynyl-2'-deoxy-2'-fluoro-2'-C-methyladenosine and its 2'-C-Methyl-ribo Analogue. Nucleic Acids Symposium Series. 52(1). 643–644. 8 indexed citations
6.
Fagan, Patrick, et al.. (2005). 2′,3′-Dideoxynucleoside 5′-β,γ-(Difluoromethylene) Triphosphates With α-P-Thio or α-P-Seleno Modifications: Synthesis and Their Inhibition of HIV-1 Reverse Transcriptase. Nucleosides Nucleotides & Nucleic Acids. 24(10-12). 1651–1664. 10 indexed citations
7.
Rajwanshi, Vivek K., Marija Prhavc, Patrick Fagan, et al.. (2005). Synthesis of 5′-Triphosphate Mimics (P3Ms) of 3′-Azido-3′,5′-Dideoxythymidine and 3′,5′-Dideoxy-5′-Difluoromethylenethymidine as HIV-1 Reverse Transcriptase Inhibitors. Nucleosides Nucleotides & Nucleic Acids. 24(3). 179–189. 5 indexed citations
8.
Rajwanshi, Vivek K., Marija Prhavc, Guangyi Wang, et al.. (2005). Synthesis of 2‘,3‘-Dideoxynucleoside 5‘-α-P-Borano-β,γ-(difluoromethylene)triphosphates and Their Inhibition of HIV-1 Reverse Transcriptase. Journal of Medicinal Chemistry. 48(7). 2695–2700. 28 indexed citations
9.
Olsen, David B., Anne B. Eldrup, Linda Bartholomew, et al.. (2004). A 7-Deaza-Adenosine Analog Is a Potent and Selective Inhibitor of Hepatitis C Virus Replication with Excellent Pharmacokinetic Properties. Antimicrobial Agents and Chemotherapy. 48(10). 3944–3953. 179 indexed citations
10.
Prhavc, Marija, Thazha P. Prakash, G. Minasov, et al.. (2003). 2‘-O-[2-[2-(N,N-Dimethylamino)ethoxy]ethyl] Modified Oligonucleotides:  Symbiosis of Charge Interaction Factors and Stereoelectronic Effects. Organic Letters. 5(12). 2017–2020. 34 indexed citations
11.
Prhavc, Marija, Balkrishen Bhat, George Just, P. Dan Cook, & Muthiah Manoharan. (2001). CHIMERIC RNA WITH MODIFIED BACKBONES: ALTERNATING METHYLENE(METHYLIMINO) LINKED PHOSPHODIESTER BACKBONE OLIGONUCLEOTIDES WITH 2′-OH AND 2′-OMe GROUPS. Nucleosides Nucleotides & Nucleic Acids. 20(4-7). 995–997. 3 indexed citations
12.
13.
Manoharan, Muthiah, Andrew M. Kawasaki, Thazha P. Prakash, et al.. (1999). Carbohydrate Modifications in Antisense Oligonucleotide Therapy: New Kids on the Block. Nucleosides and Nucleotides. 18(6-7). 1737–1746. 6 indexed citations
14.
Prhavc, Marija, Janez Plavec, J. Kobe, I. Leban, & Gerald Giester. (1999). Synthesis of a Novel Pyrazolo[1, 5-C]Pyrimidine C-Nucleoside and Conformational Analysis By NMR Spectroscopy. Nucleosides and Nucleotides. 18(11-12). 2601–2611. 1 indexed citations
15.
Prhavc, Marija & J. Kobe. (1996). SYNTHESIS OF PYRAZOLO[4,3- C ]PYRIDINE C-RIBONUCLEOSIDES VIA AN EFFECTIVE TETRAZOLE TO PYRAZOLE TRANSFORMATION. Nucleosides and Nucleotides. 15(11-12). 1779–1795. 5 indexed citations
16.
Kobe, J., et al.. (1994). Preparation and Utility of 5-β-D-Ribofuranosyl-1H-tetrazole as a Key Synthon for C-Nucleoside Synthesis. Nucleosides and Nucleotides. 13(10). 2209–2244. 7 indexed citations
17.
Prhavc, Marija, L. B. TOWNSEND, & J. Kobe. (1991). Reactions of 5-β-D-Ribofuranosyl Tetrazoles with Dipolarophiles. Nucleosides and Nucleotides. 10(1-3). 729–730. 3 indexed citations
18.
Kobe, J., et al.. (1987). The Preparation and Utility of 5-β-D-Ribofuranosyl-(2H)-Tetrazole as a Key Synthon for C-Nucleoside Chemistry. Nucleosides and Nucleotides. 6(1-2). 365–368. 4 indexed citations
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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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