David Requena

2.0k total citations · 1 hit paper
35 papers, 1.3k citations indexed

About

David Requena is a scholar working on Molecular Biology, Infectious Diseases and Immunology. According to data from OpenAlex, David Requena has authored 35 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Infectious Diseases and 6 papers in Immunology. Recurrent topics in David Requena's work include vaccines and immunoinformatics approaches (5 papers), Tuberculosis Research and Epidemiology (4 papers) and Developmental Biology and Gene Regulation (4 papers). David Requena is often cited by papers focused on vaccines and immunoinformatics approaches (5 papers), Tuberculosis Research and Epidemiology (4 papers) and Developmental Biology and Gene Regulation (4 papers). David Requena collaborates with scholars based in United States, Peru and Spain. David Requena's co-authors include Vladimir Makarov, Timothy A. Chan, Jeffrey K. Weber, David M. Hyman, Naiyer A. Rizvi, Ahmet Zehir, Edward B. Garon, Benjamin D. Greenbaum, Claud Grigg and Nadeem Riaz and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

David Requena

34 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Patient HLA class I genotype influences cancer response to checkpoint blockade immunotherapy

2017 738 citations Diego Chowell, Luc G.T. Morris et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Requena United States	16	623	427	397	221	198	35	1.3k
Tricia R. Cottrell United States	16	855 1.4×	443 1.0×	369 0.9×	131 0.6×	315 1.6×	34	1.4k
Emmanuel C. Patin United Kingdom	16	553 0.9×	664 1.6×	403 1.0×	115 0.5×	181 0.9×	22	1.4k
Dennis Kirchhoff Germany	10	707 1.1×	1.0k 2.5×	607 1.5×	251 1.1×	168 0.8×	18	1.8k
Kyoung‐Ho Pyo South Korea	21	892 1.4×	395 0.9×	418 1.1×	173 0.8×	516 2.6×	61	1.6k
Michelle H. Nelson United States	19	747 1.2×	713 1.7×	604 1.5×	123 0.6×	83 0.4×	35	1.6k
Fei Ye China	20	506 0.8×	632 1.5×	570 1.4×	138 0.6×	88 0.4×	64	1.8k
Jonathan Chang United States	10	349 0.6×	700 1.6×	332 0.8×	132 0.6×	109 0.6×	13	1.3k
Lihua Tao United States	21	627 1.0×	281 0.7×	541 1.4×	104 0.5×	101 0.5×	51	1.3k
Robert K. Bright United States	22	477 0.8×	497 1.2×	670 1.7×	202 0.9×	316 1.6×	60	1.5k
Hiroshi Kikuchi Japan	20	515 0.8×	592 1.4×	407 1.0×	184 0.8×	179 0.9×	88	1.7k

Countries citing papers authored by David Requena

Since Specialization

Citations

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

Fields of papers citing papers by David Requena

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Requena

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

Requena, David, et al.. (2024). Liver cancer multiomics reveals diverse protein kinase A disruptions convergently produce fibrolamellar hepatocellular carcinoma. Nature Communications. 15(1). 10887–10887. 2 indexed citations

Requena, David, Caroline S. Jiang, Roger Vaughan, et al.. (2023). GalNAc-conjugated siRNA targeting the DNAJB1-PRKACA fusion junction in fibrolamellar hepatocellular carcinoma. Molecular Therapy. 32(1). 140–151. 8 indexed citations

Requena, David, Søren Heissel, Hanan Alwaseem, et al.. (2023). Disruption of proteome by an oncogenic fusion kinase alters metabolism in fibrolamellar hepatocellular carcinoma. Science Advances. 9(25). eadg7038–eadg7038. 4 indexed citations

Gilman, Robert H., Vitaliano Cama, Armando E. González, et al.. (2023). Assembly and phylogeographical analysis of novel Taenia solium mitochondrial genomes suggest stratification within the African-American genotype. Parasites & Vectors. 16(1). 349–349. 2 indexed citations

Requena, David, Gadi Lalazar, Lavoisier Ramos‐Espiritu, et al.. (2022). Human liver organoids for disease modeling of fibrolamellar carcinoma. Stem Cell Reports. 17(8). 1874–1888. 18 indexed citations

Soto, Luis F., David Requena, & Juan I. Fuxman Bass. (2022). Epitope-Evaluator: An interactive web application to study predicted T-cell epitopes. PLoS ONE. 17(8). e0273577–e0273577. 5 indexed citations

Soto, Luis F., et al.. (2022). Immunoinformatic analysis of the whole proteome for vaccine design: An application to Clostridium perfringens. Frontiers in Immunology. 13. 942907–942907. 4 indexed citations

Soto, Luis F., et al.. (2020). Tear biomarkers and corneal sensitivity as an indicator of neuropathy in type 2 diabetes. Diabetes Research and Clinical Practice. 163. 108143–108143. 11 indexed citations

Zimic, Mirko, et al.. (2018). A novel inexpensive electrochemical sensor for pyrazinoic acid as a potential tool for the identification of pyrazinamide-resistant Mycobacterium tuberculosis. International Journal of Mycobacteriology. 7(3). 275–275. 5 indexed citations

10.

Kastenhuber, Edward R., Gadi Lalazar, Shauna L Houlihan, et al.. (2017). DNAJB1–PRKACA fusion kinase interacts with β-catenin and the liver regenerative response to drive fibrolamellar hepatocellular carcinoma. Proceedings of the National Academy of Sciences. 114(50). 13076–13084. 114 indexed citations

11.

Chowell, Diego, Luc G.T. Morris, Claud Grigg, et al.. (2017). Patient HLA class I genotype influences cancer response to checkpoint blockade immunotherapy. Science. 359(6375). 582–587. 738 indexed citations breakdown →

12.

Zevallos, Karine, et al.. (2017). Feasibility and Acceptability of a Text Message-Based Smoking Cessation Program for Young Adults in Lima, Peru: Pilot Study. JMIR mhealth and uhealth. 5(8). e116–e116. 15 indexed citations

13.

Requena, David, et al.. (2017). Origins and Specification of the Drosophila Wing. Current Biology. 27(24). 3826–3836.e5. 26 indexed citations

14.

Castro, Juan C., J. Dylan Maddox, Marianela Cobos, et al.. (2015). De novo assembly and functional annotation of Myrciaria dubia fruit transcriptome reveals multiple metabolic pathways for L-ascorbic acid biosynthesis. BMC Genomics. 16(1). 997–997. 25 indexed citations

15.

Kanca, Oguz, David Requena, Fisun Hamaratoǧlu, et al.. (2015). Establishment of a Developmental Compartment Requires Interactions between Three Synergistic Cis-regulatory Modules. PLoS Genetics. 11(10). e1005376–e1005376. 17 indexed citations

16.

Pajuelo, Mónica J., María Eguiluz, Eric Dahlstrom, et al.. (2015). Identification and Characterization of Microsatellite Markers Derived from the Whole Genome Analysis of Taenia solium. PLoS neglected tropical diseases. 9(12). e0004316–e0004316. 13 indexed citations

17.

Tabb, Karen M., et al.. (2014). Perceptions and Acceptability of Short Message Services Technology to Improve Treatment Adherence amongst Tuberculosis Patients in Peru: A Focus Group Study. PLoS ONE. 9(5). e95770–e95770. 36 indexed citations

18.

Requena, David, Andrés H. Gutiérrez, Ray Izquierdo-Lara, et al.. (2013). Genome sequence and comparative analysis of Avibacterium paragallinarum. Bioinformation. 9(10). 528–536. 11 indexed citations

19.

Alva-Mantari, Alicia, Fredy Aquino, Robert H. Gilman, et al.. (2013). Morphological Characterization of Mycobacterium tuberculosis in a MODS Culture for an Automatic Diagnostics through Pattern Recognition. PLoS ONE. 8(12). e82809–e82809. 15 indexed citations

20.

Quiliano, Miguel, David Requena, Andrés H. Gutiérrez, et al.. (2013). Molecular distribution of amino acid substitutions on neuraminidase from the 2009 (H1N1) human influenza pandemic virus. Bioinformation. 9(13). 673–679. 4 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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