Mark A. Pook - Concepedia

Author

Mark A. Pook

Brunel University of London ORCID

Also Known As

M A Pook, M Pook, M. A. POOK, M. A. Pook, M. Pook, MARK A POOK, Mark A Pook, Mark A. Pook, Mark Pook, Pook Mark

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Brunel University of London University College London Imperial College London Hammersmith Hospital University of Oklahoma Health Sciences Center

About

Mark A. Pook is an author at Brunel University of London specializing in medicine, genetics, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	25	1.7K
2	Natural Sciences	5	5	486
3	Engineering	1	1	40
4	Health Sciences	1	1	29
5	Public Health	1	1	10

Mark A. Pook

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues Sahar Al‐Mahdawi, Ricardo Mouro Pinto, Ozama Ismail, Human Molecular Genetics Epigenetic ChangeGeneticsDna MethylationMolecular BiologyDisease Gene Identification	2007	252
GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology Sahar Al‐Mahdawi, Ricardo Mouro Pinto, Dhaval Varshney, Genomics Neurodegenerative DiseasesDegenerative DiseaseDegenerative PathologyNeurochemical BiomarkersNeurology	2006	235
Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 3 Xi Chen, Tie-Shan Tang, Huiping Tu, Journal of Neuroscience	2008	216
Frataxin Deficiency Leads to Defects in Expression of Antioxidants and Nrf2 Expression in Dorsal Root Ganglia of the Friedreich's Ataxia YG8R Mouse Model Yuxi Shan, Robert Schoenfeld, Genki Hayashi, Antioxidants and Redox Signaling	2013	155
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. Rajesh V. Thakker, Mark A. Pook, C Wooding, Journal of Clinical Investigation Generalized Allele LossCytogeneticsGeneticsPathologyMolecular Genetics	1993	149
'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich’s ataxia' Rosella Abeti, Micheal H Parkinson, Iain P. Hargreaves, Cell Death and Disease	2016	126
Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients Irene De Biase, Astrid Rasmussen, Dan Endres, Annals of Neurology	2007	114
Prolonged treatment with pimelic o-aminobenzamide HDAC inhibitors ameliorates the disease phenotype of a Friedreich ataxia mouse model Chiranjeevi Sandi, Ricardo Mouro Pinto, Sahar Al‐Mahdawi, Neurobiology of Disease	2011	114
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22 Mark A. Pook, Oliver Wrong, C Wooding, Human Molecular Genetics Kidney StonesUrologyMendelian DisorderRenal Fanconi SyndromeGenetic Disorder	1993	104
GAA repeat instability in Friedreich ataxia YAC transgenic mice Sahar Al‐Mahdawi, Ricardo Mouro Pinto, Piers Ruddle, Genomics Knockout MouseGeneticsGaa Repeat InstabilityDegenerative Disease	2004	93

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