Luis G. Brieba

2.4k total citations
93 papers, 1.8k citations indexed

About

Luis G. Brieba is a scholar working on Molecular Biology, Infectious Diseases and Immunology. According to data from OpenAlex, Luis G. Brieba has authored 93 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 14 papers in Infectious Diseases and 13 papers in Immunology. Recurrent topics in Luis G. Brieba's work include DNA Repair Mechanisms (23 papers), DNA and Nucleic Acid Chemistry (14 papers) and RNA and protein synthesis mechanisms (13 papers). Luis G. Brieba is often cited by papers focused on DNA Repair Mechanisms (23 papers), DNA and Nucleic Acid Chemistry (14 papers) and RNA and protein synthesis mechanisms (13 papers). Luis G. Brieba collaborates with scholars based in Mexico, United States and Argentina. Luis G. Brieba's co-authors include Rui Sousa, Tom Ellenberger, Rogerio R. Sotelo‐Mundo, Robert J. Kokoska, Thomas A. Kunkel, Adrián Ochoa‐Leyva, Sylvie Doublié, Jianbin Huang, Brandt F. Eichman and Alonso A. López-Zavala and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Luis G. Brieba

89 papers receiving 1.8k citations

Peers

Luis G. Brieba

IMMUN

GENET

ECOLO

Jie Ma China

Richárd Bártfai Netherlands

Sergio H. Marshall Chile

Katharina Paschinger Austria

Hanne C. Winther‐Larsen Norway

Thomas Ziegelhoffer United States

Xiaojin Xu China

Tomomitsu Hatakeyama Japan

Aparecida S. Tanaka Brazil

Agnieszka Sierakowska Juncker Denmark

Jie Ma China

Luis G. Brieba

673 ×0.5

1.1k ×3.4

IMMUN

227 ×0.8

GENET

146 ×0.6

ECOLO

143 ×0.8

Citations per year, relative to Luis G. Brieba Luis G. Brieba (= 1×) peers Jie Ma

Countries citing papers authored by Luis G. Brieba

Since Specialization

Citations

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

Fields of papers citing papers by Luis G. Brieba

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luis G. Brieba

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

Trasviña‐Arenas, Carlos H., et al.. (2025). A steric gate prevents mutagenic dATP incorporation opposite 8‐oxo‐deoxyguanosine in mitochondrial DNA polymerases. FEBS Journal. 292(13). 3430–3448. 1 indexed citations

Trasviña‐Arenas, Carlos H., et al.. (2025). In Vitro Transcription of Plant miRNA for Structural and Processing Analysis. Methods in molecular biology. 2900. 107–116.

Sloan, Daniel B., et al.. (2024). Expansion of the MutS gene family in plants. The Plant Cell. 37(7). 3 indexed citations

Brieba, Luis G., Rosalía Lira, Eduardo Ferat‐Osorio, et al.. (2023). Starting from scratch: Step-by-step development of diagnostic tests for SARS-CoV-2 detection by RT-LAMP. PLoS ONE. 18(1). e0279681–e0279681. 6 indexed citations

Abraham‐Juárez, María Jazmín, et al.. (2023). Plant Organellar MSH1 Is a Displacement Loop–Specific Endonuclease. Plant and Cell Physiology. 65(4). 560–575. 5 indexed citations

Torres‐Larios, Alfredo, et al.. (2021). Genome-wide and structural analysis of the Myb-SHAQKYF family in Entamoeba histolytica. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1869(4). 140601–140601. 2 indexed citations

Trasviña‐Arenas, Carlos H., et al.. (2019). Plant organellar DNA polymerases repair double-stranded breaks by microhomology-mediated end-joining. Nucleic Acids Research. 47(6). 3028–3044. 46 indexed citations

Brieba, Luis G., et al.. (2019). Arabidopsis thaliana organelles mimic the T7 phage DNA replisome with specific interactions between Twinkle protein and DNA polymerases Pol1A and Pol1B. BMC Plant Biology. 19(1). 241–241. 19 indexed citations

Trasviña‐Arenas, Carlos H., et al.. (2019). Amino and carboxy-terminal extensions of yeast mitochondrial DNA polymerase assemble both the polymerization and exonuclease active sites. Mitochondrion. 49. 166–177. 8 indexed citations

10.

Trasviña‐Arenas, Carlos H., et al.. (2019). Evolution of Base Excision Repair in Entamoeba histolytica is shaped by gene loss, gene duplication, and lateral gene transfer. DNA repair. 76. 76–88. 10 indexed citations

11.

Jiménez‐Sandoval, Pedro, Gilberto Velázquez‐Juárez, Gabriela M. Montero-Morán, et al.. (2017). A competent catalytic active site is necessary for substrate induced dimer assembly in triosephosphate isomerase. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1865(11). 1423–1432. 8 indexed citations

12.

Valencia‐Sánchez, Marco Igor, Marcelino Arciniega, Anne‐Catherine Dock‐Brégeon, et al.. (2016). Structural Insights into the Polyphyletic Origins of Glycyl tRNA Synthetases. Journal of Biological Chemistry. 291(28). 14430–14446. 17 indexed citations

13.

López-Zavala, Alonso A., Claudia G. Benítez‐Cardoza, Adrián Ochoa‐Leyva, et al.. (2016). Structural insights from a novel invertebrate triosephosphate isomerase from Litopenaeus vannamei. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1864(12). 1696–1706. 16 indexed citations

14.

Velázquez‐Juárez, Gilberto, Rui Sousa, & Luis G. Brieba. (2015). The thumb subdomain of yeast mitochondrial RNA polymerase is involved in processivity, transcript fidelity and mitochondrial transcription factor binding. RNA Biology. 12(5). 514–524. 7 indexed citations

15.

Flores‐Solis, David, Ricardo C. Rodŕıguez de la Vega, Rogelio A. Hernández‐López, et al.. (2012). New Tricks of an Old Pattern. Journal of Biological Chemistry. 287(15). 12321–12330. 40 indexed citations

16.

López-Zavala, Alonso A., Enrique de la Vega, E. De la Mora, et al.. (2012). Crystallization and X-ray diffraction studies of crustacean proliferating cell nuclear antigen. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 68(11). 1367–1370. 1 indexed citations

17.

Casados‐Vázquez, Luz E., Samuel Lara‐González, & Luis G. Brieba. (2010). Crystal structure of the cysteine protease inhibitor 2 from Entamoeba histolytica: Functional convergence of a common protein fold. Gene. 471(1-2). 45–52. 10 indexed citations

18.

Brieba, Luis G., et al.. (2010). A Nuclear Family A DNA Polymerase from Entamoeba histolytica Bypasses Thymine Glycol. PLoS neglected tropical diseases. 4(8). e786–e786. 8 indexed citations

19.

Brieba, Luis G., Robert J. Kokoska, Katarzyna Bębenek, Thomas A. Kunkel, & Tom Ellenberger. (2005). A Lysine Residue in the Fingers Subdomain of T7 DNA Polymerase Modulates the Miscoding Potential of 8-Oxo-7,8-Dihydroguanosine. Structure. 13(11). 1653–1659. 35 indexed citations

20.

Brieba, Luis G., Brandt F. Eichman, Robert J. Kokoska, et al.. (2004). Structural basis for the dual coding potential of 8‐oxoguanosine by a high‐fidelity DNA polymerase. The EMBO Journal. 23(17). 3452–3461. 178 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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