Luis A. Parada

2.4k total citations
41 papers, 1.8k citations indexed

About

Luis A. Parada is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Luis A. Parada has authored 41 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Surgery and 10 papers in Genetics. Recurrent topics in Luis A. Parada's work include Cholangiocarcinoma and Gallbladder Cancer Studies (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genomics and Chromatin Dynamics (7 papers). Luis A. Parada is often cited by papers focused on Cholangiocarcinoma and Gallbladder Cancer Studies (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genomics and Chromatin Dynamics (7 papers). Luis A. Parada collaborates with scholars based in Argentina, Spain and Sweden. Luis A. Parada's co-authors include Tom Misteli, Philip G. McQueen, Peter J. Munson, Jeffrey J. Roix, Bertil Johansson, Magnus Hallén, K.‐G. Tranberg, José L. Zugaza, Felix Mitelman and Inga Hägerstrand and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Gastroenterology.

In The Last Decade

Luis A. Parada

40 papers receiving 1.8k citations

Peers

Luis A. Parada

GENET

SURGE

Vijay S. Tonk United States

Kevin J. Wu United States

Roberto Taramelli Italy

Jan C. Liang United States

Ruihong Wang United States

Raktim Sinha United States

Meena Augustus United States

Takehisa Matsumoto Japan

Toshiki Mori Japan

Vijay S. Tonk United States

Luis A. Parada

1.2k ×0.9

689 ×1.6

GENET

162 ×0.5

250 ×1.2

181 ×1.2

SURGE

Citations per year, relative to Luis A. Parada Luis A. Parada (= 1×) peers Vijay S. Tonk

Countries citing papers authored by Luis A. Parada

Since Specialization

Citations

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

Fields of papers citing papers by Luis A. Parada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luis A. Parada

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

Vicente, Mário, Noemí Tirado, Luis A. Parada, et al.. (2025). Human adaptation in the Andes Mountains.

Llavero, Francisco, David Fernández‐Moreno, Hadriano M. Lacerda, et al.. (2019). Epidermal growth factor receptor controls glycogen phosphorylase in T cells through small GTPases of the RAS family. Journal of Biological Chemistry. 294(12). 4345–4358. 12 indexed citations

Vega-Benedetti, Ana Florencia, et al.. (2016). PLAGL1: an important player in diverse pathological processes. Journal of Applied Genetics. 58(1). 71–78. 19 indexed citations

Royo, Félix, et al.. (2015). Expression of the DYRK1A gene correlates with its 3D positioning in the interphase nucleus of Down syndrome cells. Chromosome Research. 23(2). 285–298. 8 indexed citations

Bustos, María Fernanda García, Rubén O. Cimino, Rubén Marino Cardozo, et al.. (2014). In Vivo Antileishmanial Efficacy of Miltefosine AgainstLeishmania(Leishmania)amazonensis. Journal of Parasitology. 100(6). 840–847. 11 indexed citations

Davies, Carolina, Nilay Dey, Olga Sánchez Negrette, et al.. (2014). Hepatotoxicity in Mice of a Novel Anti-parasite Drug Candidate Hydroxymethylnitrofurazone: A Comparison with Benznidazole. PLoS neglected tropical diseases. 8(10). e3231–e3231. 23 indexed citations

Conde, Manuel, et al.. (2013). ATP Antagonizes Thrombin-Induced Signal Transduction through 12(S)-HETE and cAMP. PLoS ONE. 8(6). e67117–e67117. 6 indexed citations

Zabala‐Letona, Amaia, et al.. (2013). Combined Fluorescent-Chromogenic In Situ Hybridization for Identification and Laser Microdissection of Interphase Chromosomes. PLoS ONE. 8(4). e60238–e60238. 10 indexed citations

Vellón, Luciano, et al.. (2010). Functional blockade of α5β1 integrin induces scattering and genomic landscape remodeling of hepatic progenitor cells. BMC Cell Biology. 11(1). 81–81. 12 indexed citations

10.

Royo, Félix, et al.. (2009). Spatial link between nucleoli and expression of the Zac1 gene. Chromosoma. 118(6). 711–722. 12 indexed citations

11.

Parada, Luis A.. (2004). Spatial genome organization. Experimental Cell Research. 296(1). 64–70. 70 indexed citations

12.

Roix, Jeffrey J., Philip G. McQueen, Peter J. Munson, Luis A. Parada, & Tom Misteli. (2003). Spatial proximity of translocation-prone gene loci in human lymphomas. Nature Genetics. 34(3). 287–291. 320 indexed citations

13.

Diep, Chieu B., Luis A. Parada, Manuel R. Teixeira, et al.. (2002). Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G‐banding analysis. Genes Chromosomes and Cancer. 36(2). 189–197. 38 indexed citations

14.

Hallén, Magnus, Luis A. Parada, Ludmila Gorunova, et al.. (2002). Cytogenetic abnormalities in a hemangiopericytoma of the spleen. Cancer Genetics and Cytogenetics. 136(1). 62–65. 10 indexed citations

15.

Laes, Jean‐François, Luis A. Parada, Bertil Johansson, et al.. (2000). Alterations of P19ARF in Rodent Hepatoma Cell Lines but not in Human Primary Liver Cancer. Cancer Genetics and Cytogenetics. 117(2). 118–124. 1 indexed citations

16.

Parada, Luis A., Janusz Limon, Mariola Iliszko, et al.. (2000). Cytogenetics of hepatoblastoma: Further characterization of 1q rearrangements by fluorescence in situ hybridization: An international collaborative study. Medical and Pediatric Oncology. 34(3). 165–170. 31 indexed citations

17.

Parada, Luis A., Magnus Hallén, K.‐G. Tranberg, et al.. (1999). Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas. Clinical & Experimental Metastasis. 17(6). 471–479. 29 indexed citations

18.

Parada, Luis A., Magnus Hallén, K.‐G. Tranberg, et al.. (1998). Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer. Genes Chromosomes and Cancer. 23(1). 26–35. 56 indexed citations

19.

Parada, Luis A., Georgia Bardi, Magnus Hallén, et al.. (1997). Cytogenetic Abnormalities and Clonal Evolution in an Adult Hepatoblastoma. The American Journal of Surgical Pathology. 21(11). 1381–1386. 27 indexed citations

20.

Bardi, Georgia, Luis A. Parada, Nikos Pandis, et al.. (1997). Cytogenetic findings in metastases from colorectal cancer. International Journal of Cancer. 72(4). 604–607. 16 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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