Mark A. Pook

3.7k total citations
68 papers, 2.9k citations indexed

About

Mark A. Pook is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Mark A. Pook has authored 68 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 53 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Mark A. Pook's work include Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (44 papers) and DNA Repair Mechanisms (15 papers). Mark A. Pook is often cited by papers focused on Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (44 papers) and DNA Repair Mechanisms (15 papers). Mark A. Pook collaborates with scholars based in United Kingdom, United States and Italy. Mark A. Pook's co-authors include Sahar Al‐Mahdawi, Chiranjeevi Sandi, Ricardo Mouro Pinto, Rajesh V. Thakker, Dhaval Varshney, Sara Anjomani Virmouni, C Wooding, Sanjay I. Bidichandani, Irene De Biase and Vahid Ezzatizadeh and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Mark A. Pook

68 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark A. Pook United Kingdom 31 2.4k 1.8k 403 394 348 68 2.9k
Michael D. Kaytor United States 20 2.1k 0.9× 1.6k 0.9× 411 1.0× 191 0.5× 184 0.5× 37 2.6k
Nagat Bissada Canada 26 2.6k 1.1× 1.8k 1.0× 716 1.8× 256 0.6× 130 0.4× 37 3.7k
Samir Belal Tunisia 23 1.1k 0.5× 1.0k 0.6× 416 1.0× 299 0.8× 131 0.4× 61 1.9k
Pieter A. Bolhuis Netherlands 31 1.8k 0.7× 2.2k 1.2× 909 2.3× 489 1.2× 293 0.8× 63 4.0k
Mathieu Lesort United States 31 1.3k 0.5× 1.2k 0.7× 646 1.6× 321 0.8× 96 0.3× 53 2.8k
Marie‐Paule Muriel France 22 1.2k 0.5× 1.1k 0.6× 841 2.1× 287 0.7× 115 0.3× 30 2.5k
Arantxa Tabernero Spain 35 1.8k 0.7× 763 0.4× 147 0.4× 162 0.4× 159 0.5× 74 2.8k
Géraldine Liot France 21 2.2k 0.9× 1.2k 0.7× 466 1.2× 443 1.1× 129 0.4× 27 3.2k
Kambiz N. Alavian United States 25 1.7k 0.7× 543 0.3× 253 0.6× 135 0.3× 121 0.3× 46 2.4k
Kyproula Christodoulou Cyprus 23 1.2k 0.5× 930 0.5× 388 1.0× 412 1.0× 217 0.6× 85 2.1k

Countries citing papers authored by Mark A. Pook

Since Specialization
Citations

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

Fields of papers citing papers by Mark A. Pook

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark A. Pook

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. Pook. A scholar is included among the top collaborators of Mark A. Pook 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 Mark A. Pook. Mark A. Pook 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.
Abeti, Rosella, et al.. (2022). A Drug Combination Rescues Frataxin-Dependent Neural and Cardiac Pathophysiology in FA Models. Frontiers in Molecular Biosciences. 9. 830650–830650. 5 indexed citations
2.
Muñoz-Lasso, Diana C., Belén Mollá, María de la Iglesia-Vayá, et al.. (2022). Frataxin Deficit Leads to Reduced Dynamics of Growth Cones in Dorsal Root Ganglia Neurons of Friedreich’s Ataxia YG8sR Model: A Multilinear Algebra Approach. Frontiers in Molecular Neuroscience. 15. 912780–912780. 3 indexed citations
3.
Valle, Adamo, Nicholas T. Perry, Ester Kalef-Ezra, et al.. (2020). HMTase Inhibitors as a Potential Epigenetic-Based Therapeutic Approach for Friedreich’s Ataxia. Frontiers in Genetics. 11. 584–584. 6 indexed citations
4.
Fradley, Rosa, David E. Miller, Mark A. Pook, & Jordi Serrats. (2019). Preclinical Assessment of TAK-831, a Selective D-Amino Acid Oxidase Inhibitor, in a Genetic Model of Friedreich’s Ataxia (YG8sR) (P1.8-005). Neurology. 92(15_supplement). 2 indexed citations
5.
Abeti, Rosella, Iain P. Hargreaves, Plamena R. Angelova, et al.. (2016). 'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich’s ataxia'. Cell Death and Disease. 7(5). e2237–e2237. 99 indexed citations
6.
Virmouni, Sara Anjomani, Sahar Al‐Mahdawi, Chiranjeevi Sandi, et al.. (2015). Identification of telomere dysfunction in Friedreich ataxia. Molecular Neurodegeneration. 10(1). 22–22. 16 indexed citations
7.
Abeti, Rosella, et al.. (2015). Targeting lipid peroxidation and mitochondrial imbalance in Friedreich's ataxia. Pharmacological Research. 99. 344–350. 60 indexed citations
8.
Ezzatizadeh, Vahid, et al.. (2014). MutLα Heterodimers Modify the Molecular Phenotype of Friedreich Ataxia. PLoS ONE. 9(6). e100523–e100523. 20 indexed citations
9.
Hayashi, Genki, Yan Shen, Theresa L. Pedersen, et al.. (2014). Frataxin deficiency increases cyclooxygenase 2 and prostaglandins in cell and animal models of Friedreich's ataxia. Human Molecular Genetics. 23(25). 6838–6847. 28 indexed citations
10.
Sandi, Chiranjeevi, et al.. (2014). Generation and Characterisation of Friedreich Ataxia YG8R Mouse Fibroblast and Neural Stem Cell Models. PLoS ONE. 9(2). e89488–e89488. 26 indexed citations
11.
Li, Lingli, Lucille Voullaire, Chiranjeevi Sandi, et al.. (2013). Pharmacological Screening Using an FXN-EGFP Cellular Genomic Reporter Assay for the Therapy of Friedreich Ataxia. PLoS ONE. 8(2). e55940–e55940. 35 indexed citations
12.
Cao, Yun, Xiaoman Dai, Zvonimir Marelja, et al.. (2012). Novel Frataxin Isoforms May Contribute to the Pathological Mechanism of Friedreich Ataxia. PLoS ONE. 7(10). e47847–e47847. 44 indexed citations
13.
Ezzatizadeh, Vahid, Ricardo Mouro Pinto, Chiranjeevi Sandi, et al.. (2012). The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model. Neurobiology of Disease. 46(1). 165–171. 48 indexed citations
14.
Bourn, Rebecka L., Irene De Biase, Ricardo Mouro Pinto, et al.. (2012). Pms2 Suppresses Large Expansions of the (GAA·TTC)n Sequence in Neuronal Tissues. PLoS ONE. 7(10). e47085–e47085. 39 indexed citations
15.
Chen, Xi, Tie-Shan Tang, Huiping Tu, et al.. (2008). Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 3. Journal of Neuroscience. 28(48). 12713–12724. 183 indexed citations
16.
Pook, Mark A., Sahar Al‐Mahdawi, Christopher J. Carroll, et al.. (2001). Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis. Neurogenetics. 3(4). 185–193. 58 indexed citations
17.
Pang, J T, Sarah E. Lloyd, C Wooding, et al.. (1996). Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene. Human Genetics. 97(6). 732–741. 29 indexed citations
18.
Pook, Mark A., Brian Harding, David J. Porteous, et al.. (1996). EagI andNotI linking clones from human chromosomes 11 and Xp. Human Genetics. 97(6). 742–749. 3 indexed citations
19.
Thakker, Rajesh V., Mark A. Pook, C Wooding, et al.. (1993). Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.. Journal of Clinical Investigation. 91(6). 2815–2821. 115 indexed citations
20.
Pook, Mark A., S. JEREMIAH, Steven J. Scheinman, S. Povey, & Rajesh V. Thakker. (1993). Localization of the Tamm‐Horsfall glycoprotein (unomodulin) gene to chromosome 16p12.3‐16p13.11. Annals of Human Genetics. 57(4). 285–290. 27 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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