Mar Matarín

7.5k total citations
26 papers, 1.8k citations indexed

About

Mar Matarín is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Mar Matarín has authored 26 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Neurology. Recurrent topics in Mar Matarín's work include Genetic Associations and Epidemiology (7 papers), Neuroinflammation and Neurodegeneration Mechanisms (5 papers) and Alzheimer's disease research and treatments (4 papers). Mar Matarín is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Neuroinflammation and Neurodegeneration Mechanisms (5 papers) and Alzheimer's disease research and treatments (4 papers). Mar Matarín collaborates with scholars based in United Kingdom, United States and Spain. Mar Matarín's co-authors include Andrew Singleton, John Hardy, J. Raphael Gibbs, Sonja W. Scholz, Dena Hernández, Angela Britton, Hon‐Chung Fung, Javier Simón‐Sánchez, Fabienne Wavrant De Vrieze and Steven Warach and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Mar Matarín

25 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mar Matarín United Kingdom 20 712 517 457 425 309 26 1.8k
Anne Rovelet‐Lecrux France 20 804 1.1× 448 0.9× 367 0.8× 540 1.3× 288 0.9× 38 2.1k
Tobias B. Haack Germany 33 2.7k 3.8× 576 1.1× 406 0.9× 377 0.9× 523 1.7× 165 3.7k
Nathalie Brouwers Belgium 26 1.2k 1.7× 364 0.7× 421 0.9× 668 1.6× 263 0.9× 46 2.6k
Sandra Redeker Netherlands 23 779 1.1× 223 0.4× 537 1.2× 167 0.4× 993 3.2× 29 2.8k
Akinori Miyashita Japan 24 865 1.2× 311 0.6× 169 0.4× 282 0.7× 158 0.5× 70 1.6k
Grégory Raux France 19 1.1k 1.5× 562 1.1× 201 0.4× 228 0.5× 319 1.0× 27 2.3k
Satoko Miyatake Japan 29 1.5k 2.1× 766 1.5× 131 0.3× 195 0.5× 508 1.6× 146 2.4k
Gourav Roy Choudhury United States 16 435 0.6× 134 0.3× 396 0.9× 115 0.3× 210 0.7× 25 1.1k
Patrizia Amati‐Bonneau France 34 2.7k 3.7× 269 0.5× 315 0.7× 195 0.5× 550 1.8× 72 3.3k
Ilaria Guella Canada 20 454 0.6× 274 0.5× 152 0.3× 438 1.0× 255 0.8× 45 1.3k

Countries citing papers authored by Mar Matarín

Since Specialization
Citations

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

Fields of papers citing papers by Mar Matarín

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mar Matarín

This figure shows the co-authorship network connecting the top 25 collaborators of Mar Matarín. A scholar is included among the top collaborators of Mar Matarín 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 Mar Matarín. Mar Matarín 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.
Guelfi, Sebastian, Juan A. Botía, Maria Thom, et al.. (2019). Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy. Brain. 142(6). 1616–1630. 42 indexed citations
2.
Piers, Thomas M., Emma East, Claudio Villegas-Llerena, et al.. (2018). Soluble Fibrinogen Triggers Non-cell Autonomous ER Stress-Mediated Microglial-Induced Neurotoxicity. Frontiers in Cellular Neuroscience. 12. 404–404. 14 indexed citations
3.
Cummings, Damian M., Wenfei Liu, Erik Portelius, et al.. (2015). First effects of rising amyloid-β in transgenic mouse brain: synaptic transmission and gene expression. Brain. 138(7). 1992–2004. 61 indexed citations
4.
Matarín, Mar, Derviş A. Salih, Marina V. Yasvoina, et al.. (2015). A Genome-wide Gene-Expression Analysis and Database in Transgenic Mice during Development of Amyloid or Tau Pathology. Cell Reports. 10(4). 633–644. 193 indexed citations
5.
Rainger, Joe, Smita Bhatia, Hemant Bengani, et al.. (2013). Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence. Human Molecular Genetics. 23(10). 2569–2579. 46 indexed citations
6.
Meschia, James F., Andrew Singleton, Michael A. Nalls, et al.. (2011). Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis. PLoS ONE. 6(9). e23161–e23161. 12 indexed citations
7.
Biffi, A., et al.. (2010). Failure to validate association between 12p13 variants and ischemic stroke. 5 indexed citations
8.
Biffi, Alessandro, Christopher D. Anderson, Michael A. Nalls, et al.. (2010). Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics. The American Journal of Human Genetics. 86(6). 904–917. 34 indexed citations
9.
Gschwendtner, Andreas, Steve Bevan, John W. Cole, et al.. (2009). Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Annals of Neurology. 65(5). 531–539. 149 indexed citations
10.
Matarín, Mar, Andrew Singleton, John Hardy, & James F. Meschia. (2009). The genetics of ischaemic stroke. Journal of Internal Medicine. 267(2). 139–155. 39 indexed citations
11.
Nalls, Michael A., Javier Simón‐Sánchez, J. Raphael Gibbs, et al.. (2009). Measures of Autozygosity in Decline: Globalization, Urbanization, and Its Implications for Medical Genetics. PLoS Genetics. 5(3). e1000415–e1000415. 54 indexed citations
12.
Bozi, Maria, et al.. (2009). A patient with pantothenate kinase-associated neurodegeneration and supranuclear gaze palsy. Clinical Neurology and Neurosurgery. 111(8). 688–690. 6 indexed citations
13.
Defazio, Giovanni, Mar Matarín, Elizabeth Peckham, et al.. (2009). The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm. Movement Disorders. 24(4). 613–616. 26 indexed citations
14.
Matarín, Mar, Javier Simón‐Sánchez, Hon‐Chung Fung, et al.. (2008). Structural genomic variation in ischemic stroke. Neurogenetics. 9(2). 101–108. 21 indexed citations
15.
Schymick, Jennifer C., Sonja W. Scholz, Hon‐Chung Fung, et al.. (2007). Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. The Lancet Neurology. 6(4). 322–328. 153 indexed citations
16.
Matarín, Mar, W. Mark Brown, John Hardy, et al.. (2007). Association of Integrin α2 Gene Variants with Ischemic Stroke. Journal of Cerebral Blood Flow & Metabolism. 28(1). 81–89. 28 indexed citations
17.
Simón‐Sánchez, Javier, Sonja W. Scholz, Hon‐Chung Fung, et al.. (2006). Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. Human Molecular Genetics. 16(1). 1–14. 175 indexed citations
18.
Fung, Hon‐Chung, Sonja W. Scholz, Mar Matarín, et al.. (2006). Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. The Lancet Neurology. 5(11). 911–916. 284 indexed citations
19.
Mataró, María, Mar Matarín, María A. Poca, et al.. (2006). Functional and magnetic resonance imaging correlates of corpus callosum in normal pressure hydrocephalus before and after shunting. Journal of Neurology Neurosurgery & Psychiatry. 78(4). 395–398. 60 indexed citations
20.
Matarín, Mar, Andrew Singleton, & Henry Houlden. (2006). PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease. Neuroscience Letters. 407(2). 162–165. 13 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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