Marina Naval-Sánchez

2.0k total citations · 1 hit paper
29 papers, 1.1k citations indexed

About

Marina Naval-Sánchez is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Marina Naval-Sánchez has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Marina Naval-Sánchez's work include Genetic and phenotypic traits in livestock (12 papers), Genomics and Chromatin Dynamics (10 papers) and Genetic Mapping and Diversity in Plants and Animals (9 papers). Marina Naval-Sánchez is often cited by papers focused on Genetic and phenotypic traits in livestock (12 papers), Genomics and Chromatin Dynamics (10 papers) and Genetic Mapping and Diversity in Plants and Animals (9 papers). Marina Naval-Sánchez collaborates with scholars based in Australia, Belgium and Spain. Marina Naval-Sánchez's co-authors include Stein Aerts, Delphine Potier, Valerie Christiaens, Gert Hulselmans, Zeynep Kalender Atak, Bram Van de Sande, Rekin’s Janky, Dmitry Svetlichnyy, Jean‐Christophe Marine and Laura Standaert and has published in prestigious journals such as Nucleic Acids Research, Development and Journal of Agricultural and Food Chemistry.

In The Last Decade

Marina Naval-Sánchez

29 papers receiving 1.1k 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.

iRegulon: From a Gene List to a Gene Regulatory Network Using Large Motif and Track Collections

2014 610 citations Bram Van de Sande, Valerie Christiaens et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marina Naval-Sánchez Australia	14	687	253	168	121	91	29	1.1k
Sebastian M. Waszak United States	17	839 1.2×	379 1.5×	203 1.2×	113 0.9×	58 0.6×	28	1.3k
Michelle J. Doyle United States	13	837 1.2×	194 0.8×	116 0.7×	167 1.4×	57 0.6×	17	1.3k
Solenne Correard Canada	4	1000 1.5×	188 0.7×	262 1.6×	157 1.3×	46 0.5×	5	1.3k
Walter Santana-Garcia France	4	1.1k 1.6×	195 0.8×	260 1.5×	161 1.3×	41 0.5×	4	1.4k
Raquel de Sousa Abreu United States	8	1.2k 1.8×	192 0.8×	267 1.6×	166 1.4×	88 1.0×	9	1.8k
Lifang Gao China	16	556 0.8×	209 0.8×	157 0.9×	133 1.1×	59 0.6×	58	1.2k
Phillip A. Richmond Canada	11	1.4k 2.1×	387 1.5×	308 1.8×	170 1.4×	107 1.2×	25	2.0k
Eija H. Seppälä Finland	17	436 0.6×	417 1.6×	89 0.5×	88 0.7×	95 1.0×	34	1.1k
Haijing Yu China	20	798 1.2×	178 0.7×	213 1.3×	66 0.5×	37 0.4×	37	1.3k

Countries citing papers authored by Marina Naval-Sánchez

Since Specialization

Citations

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

Fields of papers citing papers by Marina Naval-Sánchez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marina Naval-Sánchez. 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 Marina Naval-Sánchez. The network helps show where Marina Naval-Sánchez may publish in the future.

Co-authorship network of co-authors of Marina Naval-Sánchez

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Naval-Sánchez, Marina, et al.. (2022). Organization of gene programs revealed by unsupervised analysis of diverse gene–trait associations. Nucleic Acids Research. 50(15). e87–e87. 4 indexed citations

Mohamed, Amin R., Marina Naval-Sánchez, Moira Menzies, et al.. (2022). Leveraging transcriptome and epigenome landscapes to infer regulatory networks during the onset of sexual maturation. BMC Genomics. 23(1). 413–413. 7 indexed citations

Wu, Zhixuan, Marina Naval-Sánchez, Xiaoli Chen, et al.. (2022). Temporal perturbation of histone deacetylase activity reveals a requirement for HDAC1–3 in mesendoderm cell differentiation. Cell Reports. 39(7). 110818–110818. 3 indexed citations

Naval-Sánchez, Marina, Minh Tran, Jingyu Zhang, et al.. (2022). Benchmarking of ATAC Sequencing Data From BGI’s Low-Cost DNBSEQ-G400 Instrument for Identification of Open and Occupied Chromatin Regions. Frontiers in Molecular Biosciences. 9. 900323–900323. 4 indexed citations

Alexandre, Pâmela A., Marina Naval-Sánchez, Moira Menzies, et al.. (2021). Chromatin accessibility and regulatory vocabulary across indicine cattle tissues. Genome biology. 22(1). 273–273. 23 indexed citations

Naval-Sánchez, Marina, Laércio R. Porto-Neto, Diércles F. Cardoso, et al.. (2020). Selection signatures in tropical cattle are enriched for promoter and coding regions and reveal missense mutations in the damage response gene HELB. Genetics Selection Evolution. 52(1). 27–27. 25 indexed citations

Naval-Sánchez, Marina, Sean McWilliam, Bradley S. Evans, et al.. (2020). Changed Patterns of Genomic Variation Following Recent Domestication: Selection Sweeps in Farmed Atlantic Salmon. Frontiers in Genetics. 11. 264–264. 19 indexed citations

Alexandre, Pâmela A., Nicholas J. Hudson, Sigrid A. Lehnert, et al.. (2020). Genome-Wide Co-Expression Distributions as a Metric to Prioritize Genes of Functional Importance. Genes. 11(10). 1231–1231. 2 indexed citations

Reverter, Antônio, et al.. (2020). Dynamics of Gene Co-expression Networks in Time-Series Data: A Case Study in Drosophila melanogaster Embryogenesis. Frontiers in Genetics. 11. 517–517. 7 indexed citations

10.

Alexandre, Pâmela A., Marina Naval-Sánchez, Laércio R. Porto-Neto, et al.. (2019). Systems Biology Reveals NR2F6 and TGFB1 as Key Regulators of Feed Efficiency in Beef Cattle. Frontiers in Genetics. 10. 230–230. 36 indexed citations

11.

Nguyen, Quan, Ross L. Tellam, Marina Naval-Sánchez, et al.. (2018). Mammalian genomic regulatory regions predicted by utilizing human genomics, transcriptomics, and epigenetics data. GigaScience. 7(3). 1–17. 26 indexed citations

12.

Kijas, James, Sean McWilliam, Marina Naval-Sánchez, et al.. (2018). Evolution of Sex Determination Loci in Atlantic Salmon. Scientific Reports. 8(1). 5664–5664. 36 indexed citations

13.

Hudson, Nicholas J., Marina Naval-Sánchez, Laércio R. Porto-Neto, Miguel Pérez‐Enciso, & Antônio Reverter. (2018). RAPID COMMUNICATION: A haplotype information theory method reveals genes of evolutionary interest in European vs. Asian pigs1. Journal of Animal Science. 96(8). 3064–3069. 3 indexed citations

14.

Naval-Sánchez, Marina, Delphine Potier, Paulo S. Pereira, et al.. (2017). Nuclear receptors connect progenitor transcription factors to cell cycle control. Scientific Reports. 7(1). 4845–4845. 12 indexed citations

15.

Naval-Sánchez, Marina, Delphine Potier, Gert Hulselmans, Valerie Christiaens, & Stein Aerts. (2015). Identification of Lineage-SpecificCis-Regulatory Modules Associated with Variation in Transcription Factor Binding and Chromatin Activity Using Ornstein–Uhlenbeck Models. Molecular Biology and Evolution. 32(9). 2441–2455. 8 indexed citations

16.

Potier, Delphine, Kristofer Davie, Gert Hulselmans, et al.. (2014). Mapping Gene Regulatory Networks in Drosophila Eye Development by Large-Scale Transcriptome Perturbations and Motif Inference. Cell Reports. 9(6). 2290–2303. 50 indexed citations

17.

Broeck, Lies Vanden, Marina Naval-Sánchez, Yoshitsugu Adachi, et al.. (2013). TDP-43 Loss-of-Function Causes Neuronal Loss Due to Defective Steroid Receptor-Mediated Gene Program Switching in Drosophila. Cell Reports. 3(1). 160–172. 52 indexed citations

18.

Naval-Sánchez, Marina, Delphine Potier, Sebastian Munck, et al.. (2012). Comparative motif discovery combined with comparative transcriptomics yields accurate targetome and enhancer predictions. Genome Research. 23(1). 74–88. 25 indexed citations

19.

Potier, Delphine, Zeynep Kalender Atak, Marina Naval-Sánchez, Carl Herrmann, & Stein Aerts. (2011). Using cisTargetX to Predict Transcriptional Targets and Networks in Drosophila. Methods in molecular biology. 786. 291–314. 11 indexed citations

20.

Aerts, Stein, Xiao‐Jiang Quan, Annelies Claeys, et al.. (2010). Robust Target Gene Discovery through Transcriptome Perturbations and Genome-Wide Enhancer Predictions in Drosophila Uncovers a Regulatory Basis for Sensory Specification. PLoS Biology. 8(7). e1000435–e1000435. 73 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.

Explore authors with similar magnitude of impact