Elisavet Preza

2.0k total citations
13 papers, 614 citations indexed

About

Elisavet Preza is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Elisavet Preza has authored 13 papers receiving a total of 614 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Neurology and 5 papers in Physiology. Recurrent topics in Elisavet Preza's work include Mitochondrial Function and Pathology (7 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Alzheimer's disease research and treatments (4 papers). Elisavet Preza is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Alzheimer's disease research and treatments (4 papers). Elisavet Preza collaborates with scholars based in United Kingdom, Spain and United States. Elisavet Preza's co-authors include Selina Wray, Andrey Y. Abramov, Henry Houlden, John Hardy, Vincent Plagnol, Nicholas Wood, Kailash P. Bhatia, Daniah Trabzuni, Nick C. Fox and Mina Ryten and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and PLoS ONE.

In The Last Decade

Elisavet Preza

13 papers receiving 602 citations

Peers

Countries citing papers authored by Elisavet Preza

Since Specialization

Citations

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

Fields of papers citing papers by Elisavet Preza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisavet Preza

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Disruption of ER‐mitochondria tethering and signalling in C9orf72‐associated amyotrophic lateral sclerosis and frontotemporal dementia 2022 ·Aging Cell ·Patricia Gómez‐Suaga, Gábor M. Mórotz, Andrea Markovinović, Sandra M. Martín‐Guerrero, Elisavet Preza, Natalia Arias, (unknown), (unknown), (unknown), Agnes L. Nishimura, (unknown), Youn‐Bok Lee, Jacqueline C. Mitchell, Selina Wray, Christopher E. Shaw, Wendy Noble, Christopher C.J. Miller	46
2	Investigating changes in the proteostasis capabilities of iPSC‐neurons during development and in FTD using iPSC‐neurons with MAPT mutations 2021 ·Alzheimer s & Dementia ·(unknown), Charles Arber, Elisavet Preza, Claire A. Leckey, Natura Myeku, Jackie M. Casey, Michael S. Perkinton, Selina Wray	1
3	Modelling frontotemporal dementia using patient-derived induced pluripotent stem cells 2020 ·Molecular and Cellular Neuroscience ·(unknown), Jackie M. Casey, Elisavet Preza, Selina Wray	20
4	Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate During Seizure-Like Activity 2018 ·Molecular Neurobiology ·Stjepana Kovac, Elisavet Preza, Henry Houlden, Matthew C. Walker, Andrey Y. Abramov	9
5	Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neurons 2017 ·Journal of Biological Chemistry ·Marthe H. R. Ludtmann, Charles Arber, Fernando Benito Bartolomé, (unknown), Elisavet Preza, Eva Carro, Henry Houlden, Sonia Gandhi, Selina Wray, Andrey Y. Abramov	30
6	iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease 2017 ·PLoS ONE ·Charles Arber, Plamena R. Angelova, Sarah Wiethoff, Yugo Tsuchiya, Francesca Mazzacuva, Elisavet Preza, Kailash P. Bhatia, Kevin Mills, Ivan Gout, Andrey Y. Abramov, John Hardy, James A. Duce, Henry Houlden, Selina Wray	40
7	Review: Induced pluripotent stem cell models of frontotemporal dementia 2016 ·Neuropathology and Applied Neurobiology ·Elisavet Preza, John Hardy, Thomas T. Warner, Selina Wray	9
8	Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT 2015 ·Human Molecular Genetics ·(unknown), Elisavet Preza, Colin Mahoney, Núria Setó‐Salvia, Natalie S. Ryan, Huw R. Morris, Charles Arber, Michael J. Devine, Henry Houlden, Thomas T. Warner, Trevor J. Bushell, Michele Zagnoni, Tilo Kunath, Frederick J. Livesey, Nick C. Fox, Martin N. Rossor, John Hardy, Selina Wray	101
9	Higher Mitochondrial Membrane Potential Induces ROS Production in the Familiar Form of Frontotemporal Dementia with MAPT Mutations 2015 ·Biophysical Journal ·Noemí Esteras, Selina Wray, Elisavet Preza, Andrey Y. Abramov	4
10	Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy 2013 ·Journal of Neurology Neurosurgery & Psychiatry ·Arianna Tucci, (unknown), Elisavet Preza, Robert D. S. Pitceathly, Annapurna Chalasani, Vincent Plagnol, (unknown), Daniah Trabzuni, Mina Ryten, (unknown), Zane Jaunmuktane, Mary M. Reilly, Sebastian Brandner, Iain P. Hargreaves, John Hardy, (unknown), Andrey Y. Abramov, Henry Houlden	34
11	Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels 2013 ·Neuron ·Fernando Benito Bartolomé, Hsiu-Chuan Wu, Victoria Burchell, Elisavet Preza, Selina Wray, Colin Mahoney, Nick C. Fox, Andrea Calvo, Antonio Canosa, Cristina Moglia, Jessica Mandrioli, Adriano Chiò, Richard W. Orrell, Henry Houlden, John Hardy, Andrey Y. Abramov, Hélène Plun‐Favreau	121
12	Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation 2013 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), Joshua Hersheson, Vincent Plagnol, Katherine A. Fawcett, Kate Duberley, Elisavet Preza, Iain P. Hargreaves, Annapurna Chalasani, Matilde Laurá, Nicholas Wood, Mary M. Reilly, Henry Houlden	43
13	Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis 2012 ·The American Journal of Human Genetics ·Gavin Charlesworth, Vincent Plagnol, Kira M. Holmström, José Brás, Una‐Marie Sheerin, Elisavet Preza, Ignacio Rubio‐Agusti, Mina Ryten, Susanne A. Schneider, María Stamelou, Daniah Trabzuni, Andrey Y. Abramov, Kailash P. Bhatia, Nicholas Wood	156

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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