David Landeira

1.3k total citations
19 papers, 624 citations indexed

About

David Landeira is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, David Landeira has authored 19 papers receiving a total of 624 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 4 papers in Epidemiology and 2 papers in Genetics. Recurrent topics in David Landeira's work include Epigenetics and DNA Methylation (11 papers), Pluripotent Stem Cells Research (6 papers) and Genomics and Chromatin Dynamics (6 papers). David Landeira is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), Pluripotent Stem Cells Research (6 papers) and Genomics and Chromatin Dynamics (6 papers). David Landeira collaborates with scholars based in Spain, United Kingdom and United States. David Landeira's co-authors include Miguel Navarro, Amanda G. Fisher, Matthias Merkenschlager, Tomomi Tsubouchi, Francesco M. Piccolo, Jean-Mathieu Bart, Daria Van Tyne, Xenia Peñate, Natalie K. Ryan and Ludovica Bruno and has published in prestigious journals such as Cell, Nature Communications and Nature Genetics.

In The Last Decade

David Landeira

19 papers receiving 621 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Landeira Spain 12 479 147 106 64 55 19 624
Hans-Rudolf Hotz Switzerland 15 555 1.2× 196 1.3× 93 0.9× 45 0.7× 70 1.3× 21 713
Mehrdad Pedram United States 12 272 0.6× 79 0.5× 149 1.4× 66 1.0× 106 1.9× 17 517
George K. Arhin United States 10 473 1.0× 213 1.4× 64 0.6× 25 0.4× 44 0.8× 12 586
François McNicoll Germany 12 420 0.9× 273 1.9× 322 3.0× 37 0.6× 64 1.2× 19 681
Danae Schulz United States 8 252 0.5× 116 0.8× 66 0.6× 30 0.5× 55 1.0× 19 408
Bo Gustav Lindberg Sweden 7 232 0.5× 45 0.3× 97 0.9× 29 0.5× 50 0.9× 10 462
Minoru Oshiro Japan 10 196 0.4× 144 1.0× 135 1.3× 50 0.8× 18 0.3× 18 448
M. Laurent France 10 296 0.6× 322 2.2× 207 2.0× 47 0.7× 48 0.9× 14 578
Eugene Gan United States 11 464 1.0× 69 0.5× 51 0.5× 40 0.6× 37 0.7× 14 583
Kaylen Lott United States 9 438 0.9× 102 0.7× 25 0.2× 38 0.6× 30 0.5× 9 552

Countries citing papers authored by David Landeira

Since Specialization
Citations

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

Fields of papers citing papers by David Landeira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Landeira

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

All Works

19 of 19 papers shown
1.
López-Onieva, Lourdes, et al.. (2024). EZH2 represses mesenchymal genes and upholds the epithelial state of breast carcinoma cells. Cell Death and Disease. 15(8). 609–609. 3 indexed citations
2.
Alcázar‐Fabra, María, et al.. (2024). The molecular basis of cell memory in mammals: The epigenetic cycle. Science Advances. 10(9). eadl3188–eadl3188. 13 indexed citations
3.
Garrido-Navas, M. Carmen, Diego de Miguel‐Pérez, Bernardino Alcázar Navarrete, et al.. (2024). Resectable Non-Small Cell Lung Cancer Heterogeneity and Recurrence Assessed by Tissue Next-Generation Sequencing Genotyping and Circulating Tumor Cell EZH2 Characterization. Archivos de Bronconeumología. 61(3). 156–165. 1 indexed citations
4.
Alcázar‐Fabra, María, Lourdes López-Onieva, Emilia Dimitrova, et al.. (2023). Changes in PRC1 activity during interphase modulate lineage transition in pluripotent cells. Nature Communications. 14(1). 180–180. 2 indexed citations
5.
Montes, Rosa, Adrián García-Moreno, José A. López‐Escámez, et al.. (2023). The pediatric leukemia oncoprotein NUP98-KDM5A induces genomic instability that may facilitate malignant transformation. Cell Death and Disease. 14(6). 357–357. 6 indexed citations
6.
López-Onieva, Lourdes, Jordi Martorell‐Marugán, Carmen Griñán‐Lisón, et al.. (2022). EZH2 endorses cell plasticity to non-small cell lung cancer cells facilitating mesenchymal to epithelial transition and tumour colonization. Oncogene. 41(28). 3611–3624. 18 indexed citations
7.
Bleckwehl, Tore, Patricia Respuela, Sara Cruz-Molina, et al.. (2021). Orphan CpG islands amplify poised enhancer regulatory activity and determine target gene responsiveness. Nature Genetics. 53(7). 1036–1049. 62 indexed citations
8.
López-Onieva, Lourdes, et al.. (2020). Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells. Science Advances. 6(10). eaay4768–eaay4768. 34 indexed citations
9.
Martorell‐Marugán, Jordi, Rosa Montes, Verónica Ramos–Mejía, et al.. (2020). The molecular clock protein Bmal1 regulates cell differentiation in mouse embryonic stem cells. Life Science Alliance. 3(5). e201900535–e201900535. 12 indexed citations
10.
Silvente, Francisco Requena, et al.. (2019). NOMePlot: analysis of DNA methylation and nucleosome occupancy at the single molecule. Scientific Reports. 9(1). 8140–8140. 2 indexed citations
11.
Landeira, David, Hakan Bagci, Andrzej Malinowski, et al.. (2015). Jarid2 Coordinates Nanog Expression and PCP/Wnt Signaling Required for Efficient ESC Differentiation and Early Embryo Development. Cell Reports. 12(4). 573–586. 37 indexed citations
12.
Tsubouchi, Tomomi, Karen Brown, Francesco M. Piccolo, et al.. (2013). DNA Synthesis Is Required for Reprogramming Mediated by Stem Cell Fusion. Cell. 152(4). 873–883. 60 indexed citations
13.
Piccolo, Francesco M., Hakan Bagci, Karen Brown, et al.. (2013). Different Roles for Tet1 and Tet2 Proteins in Reprogramming-Mediated Erasure of Imprints Induced by EGC Fusion. Molecular Cell. 49(6). 1023–1033. 2 indexed citations
14.
Landeira, David & Amanda G. Fisher. (2010). Inactive yet indispensable: the tale of Jarid2. Trends in Cell Biology. 21(2). 74–80. 68 indexed citations
15.
Pereira, Carlos‐Filipe, Francesco M. Piccolo, Tomomi Tsubouchi, et al.. (2010). ESCs Require PRC2 to Direct the Successful Reprogramming of Differentiated Cells toward Pluripotency. Cell stem cell. 6(6). 547–556. 130 indexed citations
16.
Peñate, Xenia, et al.. (2009). RNA pol II subunit RPB7 is required for RNA pol I‐mediated transcription in Trypanosoma brucei. EMBO Reports. 10(3). 252–257. 11 indexed citations
17.
Landeira, David, Jean-Mathieu Bart, Daria Van Tyne, & Miguel Navarro. (2009). Cohesin regulates VSG monoallelic expression in trypanosomes. The Journal of Cell Biology. 186(2). 243–254. 61 indexed citations
18.
Landeira, David & Miguel Navarro. (2007). Nuclear repositioning of the VSG promoter during developmental silencing in Trypanosoma brucei. The Journal of Cell Biology. 176(2). 133–139. 65 indexed citations
19.
Navarro, Miguel, Xenia Peñate, & David Landeira. (2007). Nuclear architecture underlying gene expression in Trypanosoma brucei. Trends in Microbiology. 15(6). 263–270. 37 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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