Michael A. Farrell

4.9k total citations
24 papers, 1.3k citations indexed

About

Michael A. Farrell is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Michael A. Farrell has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Genetics. Recurrent topics in Michael A. Farrell's work include Genetics and Neurodevelopmental Disorders (5 papers), Glioma Diagnosis and Treatment (4 papers) and MicroRNA in disease regulation (4 papers). Michael A. Farrell is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Glioma Diagnosis and Treatment (4 papers) and MicroRNA in disease regulation (4 papers). Michael A. Farrell collaborates with scholars based in Ireland, Spain and Germany. Michael A. Farrell's co-authors include Norman Delanty, Donncha F. O’Brien, David C. Henshall, Amre Shahwan, Tobías Engel, Eva M. Jiménez‐Mateos, Ronán Conroy, Raymond L. Stallings, Takanori Sano and Ross C. McKiernan and has published in prestigious journals such as Nature Medicine, Nature Communications and Journal of Neuroscience.

In The Last Decade

Michael A. Farrell

23 papers receiving 1.3k citations

Peers

Michael A. Farrell

CMN

PMH

GENET

Amaya Sanz‐Rodriguez Ireland

Cécile Delarasse France

Uwe Ueberham Germany

Victoria A. Rafalski United States

Jackelien van Scheppingen Netherlands

Elena Ambrosini Italy

Peter Gebicke-Härter Germany

Karen I. Guerin United States

John F. Harms United States

Angelika Mühlebner Netherlands

Amaya Sanz‐Rodriguez Ireland

Michael A. Farrell

494 ×0.7

294 ×0.6

258 ×1.0

CMN

279 ×1.1

PMH

161 ×0.7

GENET

Citations per year, relative to Michael A. Farrell Michael A. Farrell (= 1×) peers Amaya Sanz‐Rodriguez

Countries citing papers authored by Michael A. Farrell

Since Specialization

Citations

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

Fields of papers citing papers by Michael A. Farrell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael A. Farrell

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

Mamad, Omar, Albert Sanfeliu, Amaya Sanz‐Rodriguez, et al.. (2024). Impact of JQ1 treatment on seizures, hippocampal gene expression, and gliosis in a mouse model of temporal lobe epilepsy. European Journal of Neuroscience. 60(6). 5266–5283. 2 indexed citations

Leister, Hanna, Norman Delanty, Francesca Brett, et al.. (2023). Immunoproteasome deficiency results in age-dependent development of epilepsy. Brain Communications. 6(1). fcae017–fcae017. 3 indexed citations

Greene, Chris, Nicole Hanley, Cristina R. Reschke, et al.. (2022). Microvascular stabilization via blood-brain barrier regulation prevents seizure activity. Nature Communications. 13(1). 2003–2003. 101 indexed citations

Parras, Alberto, Laura de Diego-García, Edward Beamer, et al.. (2020). Polyadenylation of mRNA as a novel regulatory mechanism of gene expression in temporal lobe epilepsy. Brain. 143(7). 2139–2153. 11 indexed citations

Fearon, Conor, et al.. (2019). Impact of the 2016 World Health Organization Classification of Tumours of the Central Nervous System: an Irish experience. Irish Journal of Medical Science (1971 -). 189(3). 799–803. 2 indexed citations

Looze, Céline De, Jane Cryan, Patrick G. Buckley, et al.. (2018). Machine learning: a useful radiological adjunct in determination of a newly diagnosed glioma’s grade and IDH status. Journal of Neuro-Oncology. 139(2). 491–499. 32 indexed citations

Raoof, Rana, Eva M. Jiménez‐Mateos, Sebastian Bauer, et al.. (2017). Cerebrospinal fluid microRNAs are potential biomarkers of temporal lobe epilepsy and status epilepticus. Scientific Reports. 7(1). 3328–3328. 94 indexed citations

Kearney, Hugh, et al.. (2017). Temporal stability of MGMT promoter methylation in glioblastoma patients undergoing STUPP protocol. Journal of Neuro-Oncology. 137(2). 233–240. 10 indexed citations

Mooney, Claire, Eva M. Jiménez‐Mateos, Tobías Engel, et al.. (2017). RNA sequencing of synaptic and cytoplasmic Upf1-bound transcripts supports contribution of nonsense-mediated decay to epileptogenesis. Scientific Reports. 7(1). 41517–41517. 15 indexed citations

10.

Jimenez‐Pacheco, Alba, Miguel Díaz‐Hernández, Marina Arribas-Blázquez, et al.. (2016). Transient P2X7 Receptor Antagonism Produces Lasting Reductions in Spontaneous Seizures and Gliosis in Experimental Temporal Lobe Epilepsy. Journal of Neuroscience. 36(22). 5920–5932. 131 indexed citations

11.

Reschke, Cristina R., Luiz Fernando Almeida Silva, Braxton A. Norwood, et al.. (2016). Potent Anti-seizure Effects of Locked Nucleic Acid Antagomirs Targeting miR-134 in Multiple Mouse and Rat Models of Epilepsy. Molecular Therapy — Nucleic Acids. 6. 45–56. 65 indexed citations

12.

Engel, Tobías, Eva M. Jiménez‐Mateos, Caoimhín G. Concannon, et al.. (2013). CHOP regulates the p53–MDM2 axis and is required for neuronal survival after seizures. Brain. 136(2). 577–592. 77 indexed citations

13.

McKiernan, Ross C., Eva M. Jiménez‐Mateos, Isabella Bray, et al.. (2012). Reduced Mature MicroRNA Levels in Association with Dicer Loss in Human Temporal Lobe Epilepsy with Hippocampal Sclerosis. PLoS ONE. 7(5). e35921–e35921. 105 indexed citations

14.

Jiménez‐Mateos, Eva M., Tobías Engel, Paula Merino‐Serrais, et al.. (2012). Silencing microRNA-134 produces neuroprotective and prolonged seizure-suppressive effects. Nature Medicine. 18(7). 1087–1094. 383 indexed citations

15.

McCoy, Bláthnaid, Cormac Owens, Stephanie Ryan, et al.. (2011). Partial status epilepticus – Rapid genetic diagnosis of Alpers’ disease. European Journal of Paediatric Neurology. 15(6). 558–562. 8 indexed citations

16.

Doherty, Colin P., Michael A. Farrell, M Fitzsimons, et al.. (2010). The Irish epilepsy surgery experience: Long-term follow-up. Seizure. 19(4). 247–252. 23 indexed citations

17.

Ryan, Aisling, James J. Ryan, Orla Hardiman, et al.. (2009). Vacuolar leucoencephalopathy and pulvinar sign in association with coeliac disease. BMJ Case Reports. 2009. bcr0820080650–bcr0820080650. 3 indexed citations

18.

Shahwan, Amre, Michael A. Farrell, & Norman Delanty. (2005). Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects. The Lancet Neurology. 4(4). 239–248. 154 indexed citations

19.

Horan, Gail, Catherine Keohane, Sophie Molloy, et al.. (2004). Creutzfeldt-Jakob Disease in Ireland: Epidemiological Aspects 1980–2002. European Neurology. 51(3). 132–137. 5 indexed citations

20.

Molloy, Sophie, et al.. (2000). The “Pulvinar” Sign in Variant Creutzfeldt-Jakob Disease. American Journal of Roentgenology. 175(2). 555–556. 7 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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