Ligia Mateiu

1.1k total citations
29 papers, 480 citations indexed

About

Ligia Mateiu is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ligia Mateiu has authored 29 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ligia Mateiu's work include Epigenetics and DNA Methylation (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Ligia Mateiu is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). Ligia Mateiu collaborates with scholars based in Belgium, United States and Spain. Ligia Mateiu's co-authors include Bruce Rannala, Amanda Ramos, María Pilar Aluja, Cristina Santos, Luis Álvarez, María del Mar González, Joris Vermeesch, Thierry Voet, Parveen Kumar and Niels van der Aa and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Ligia Mateiu

23 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ligia Mateiu Belgium 12 285 157 98 57 46 29 480
Glen R. Monroe Netherlands 12 216 0.8× 313 2.0× 44 0.4× 28 0.5× 56 1.2× 20 524
Emily Spencer United States 11 208 0.7× 214 1.4× 22 0.2× 18 0.3× 106 2.3× 15 489
Marija Volk Slovenia 14 155 0.5× 115 0.7× 76 0.8× 19 0.3× 35 0.8× 36 378
Pablo García‐Miranda Spain 13 281 1.0× 45 0.3× 19 0.2× 41 0.7× 41 0.9× 33 486
Ho‐Ming Luk China 13 249 0.9× 267 1.7× 100 1.0× 10 0.2× 24 0.5× 67 471
Dalia Ghoneim United States 10 277 1.0× 125 0.8× 19 0.2× 31 0.5× 43 0.9× 15 409
U Gruber‐Sedlmayr Austria 9 147 0.5× 97 0.6× 17 0.2× 53 0.9× 10 0.2× 17 384
Jonathan J. Wilde United States 7 305 1.1× 114 0.7× 54 0.6× 32 0.6× 24 0.5× 7 429
Paul Kuentz France 11 189 0.7× 157 1.0× 35 0.4× 16 0.3× 11 0.2× 32 323
Leopoldo Staiano Italy 11 265 0.9× 80 0.5× 21 0.2× 20 0.4× 19 0.4× 16 611

Countries citing papers authored by Ligia Mateiu

Since Specialization
Citations

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

Fields of papers citing papers by Ligia Mateiu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ligia Mateiu

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

All Works

20 of 20 papers shown
1.
Mateiu, Ligia, et al.. (2025). RNA sequencing offers new diagnostic opportunities in neurodevelopmental disorders: A systematic review. Genetics in Medicine. 28(4). 101666–101666.
2.
Laere, Steven Van, Emilie Logie, Steven Timmermans, et al.. (2025). Gradual DNA methylation changes reveal transcription factors implicated in metabolic dysfunction-associated steatotic liver disease progression and epigenetic age acceleration. Clinical Epigenetics. 17(1). 138–138. 1 indexed citations
3.
Ibrahim, Joe, et al.. (2025). Comparison of current methods for genome-wide DNA methylation profiling. Epigenetics & Chromatin. 18(1). 57–57. 5 indexed citations
4.
Rademaeker, Marjan De, et al.. (2025). Paracentric inversion disrupting the SHANK2 gene. European Journal of Medical Genetics. 75. 105009–105009.
5.
Szewczyk, Krystyna, Esther Bartholomeus, Eva Lion, et al.. (2025). Time-Series Transcriptome Analysis of the Older Adult Mouse Cochlea After Noise-Induced Hearing Loss Reveals an Acute Immune Response and Recovery-Associated Pathways. Molecular Neurobiology. 63(1). 124–124.
6.
Dijck, Anke Van, Ellen Elinck, Alexander J.M. Dingemans, et al.. (2025). A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study. Clinical Epigenetics. 17(1). 185–185.
7.
Elinck, Ellen, Jasper J. van der Smagt, Mariëlle Alders, et al.. (2024). Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel–Van der Aa syndrome. European Journal of Human Genetics. 32(6). 630–638. 4 indexed citations
8.
Beysen, Diane, Berten Ceulemans, Filip Roelens, et al.. (2024). The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study. Pediatric Neurology. 161. 1–8. 1 indexed citations
9.
Vanderhaeghen, Tineke, Cédric Peleman, Joe Ibrahim, et al.. (2024). Loss of PPARα function promotes epigenetic dysregulation of lipid homeostasis driving ferroptosis and pyroptosis lipotoxicity in metabolic dysfunction associated Steatotic liver disease (MASLD). SHILAP Revista de lepidopterología. 3. 1283170–1283170. 3 indexed citations
10.
11.
Dijck, Anke Van, Joe Ibrahim, Ellen Elinck, et al.. (2024). ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case. Acta Neuropathologica Communications. 12(1). 62–62. 9 indexed citations
12.
Mateiu, Ligia, Ellen Elinck, Michael K. McCormack, et al.. (2024). Identification of a DLG3 stop mutation in the MRX20 family. European Journal of Human Genetics. 32(3). 317–323. 1 indexed citations
13.
Ibrahim, Joe, Ligia Mateiu, Tim De Pooter, et al.. (2023). Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy. International Journal of Molecular Sciences. 24(22). 16412–16412. 10 indexed citations
14.
Hendrickx, Gretl, Eveline Boudin, Ligia Mateiu, et al.. (2023). An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone Remodeling. Calcified Tissue International. 114(2). 171–181. 1 indexed citations
15.
Lent, Jonas Van, Peter Verstraelen, Bob Asselbergh, et al.. (2021). Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction. Brain. 144(8). 2471–2485. 32 indexed citations
16.
Wei, Na, Maria‐Luise Erfurth, Ligia Mateiu, et al.. (2019). Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy. Nature Communications. 10(1). 5045–5045. 21 indexed citations
17.
Geuens, Thomas, Vicky De Winter, Nicholas Rajan, et al.. (2017). Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease. Acta Neuropathologica Communications. 5(1). 5–5. 22 indexed citations
18.
Ramos, Amanda, Ligia Mateiu, María del Mar González, et al.. (2011). Nuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studies. Mitochondrion. 11(6). 946–953. 35 indexed citations
19.
20.
Mateiu, Ligia & Bruce Rannala. (2008). Bayesian Inference of Errors in Ancient DNA Caused by Postmortem Degradation. Molecular Biology and Evolution. 25(7). 1503–1511. 15 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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