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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
2007 1
2008 3
2010 3
2011 5
2012 8
2013 7
2014 2
2015 8
2016 4
2017 6
2018 4
2019 4
2020 3
2021 2
2022 0
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Search Results

53 results
Results by year
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Page 1
Germline selection shapes human mitochondrial DNA diversity.
Wei W, Tuna S, Keogh MJ, Smith KR, Aitman TJ, Beales PL, Bennett DL, Gale DP, Bitner-Glindzicz MAK, Black GC, Brennan P, Elliott P, Flinter FA, Floto RA, Houlden H, Irving M, Koziell A, Maher ER, Markus HS, Morrell NW, Newman WG, Roberts I, Sayer JA, Smith KGC, Taylor JC, Watkins H, Webster AR, Wilkie AOM, Williamson C; NIHR BioResource–Rare Diseases; 100,000 Genomes Project–Rare Diseases Pilot, Ashford S, Penkett CJ, Stirrups KE, Rendon A, Ouwehand WH, Bradley JR, Raymond FL, Caulfield M, Turro E, Chinnery PF. Wei W, et al. Among authors: keogh mj. Science. 2019 May 24;364(6442):eaau6520. doi: 10.1126/science.aau6520. Epub 2019 May 23. Science. 2019. PMID: 31123110 Free article.
Neuroferritinopathy.
Keogh MJ, Morris CM, Chinnery PF. Keogh MJ, et al. Int Rev Neurobiol. 2013;110:91-123. doi: 10.1016/B978-0-12-410502-7.00006-5. Int Rev Neurobiol. 2013. PMID: 24209436 Review.
Mitochondrial DNA mutations in neurodegeneration.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Biochim Biophys Acta. 2015 Nov;1847(11):1401-11. doi: 10.1016/j.bbabio.2015.05.015. Epub 2015 May 23. Biochim Biophys Acta. 2015. PMID: 26014345 Free article. Review.
Exome sequencing: how to understand it.
Keogh MJ, Daud D, Chinnery PF. Keogh MJ, et al. Pract Neurol. 2013 Dec;13(6):399-407. doi: 10.1136/practneurol-2012-000498. Epub 2013 Jun 1. Pract Neurol. 2013. PMID: 23727621 Review. No abstract available.
How to spot mitochondrial disease in adults.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Clin Med (Lond). 2013 Feb;13(1):87-92. doi: 10.7861/clinmedicine.13-1-87. Clin Med (Lond). 2013. PMID: 23472503 Free PMC article. Review. No abstract available.
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP.
Nolan M, Barbagallo P, Turner MR, Keogh MJ, Chinnery PF, Talbot K, Ansorge O. Nolan M, et al. Among authors: keogh mj. J Neurol Neurosurg Psychiatry. 2021 Sep;92(9):1022-1024. doi: 10.1136/jnnp-2020-325803. Epub 2021 Mar 16. J Neurol Neurosurg Psychiatry. 2021. PMID: 33727253 Free PMC article. No abstract available.
Exome sequencing in dementia with Lewy bodies.
Keogh MJ, Kurzawa-Akanbi M, Griffin H, Douroudis K, Ayers KL, Hussein RI, Hudson G, Pyle A, Cordell HJ, Attems J, McKeith IG, O'Brien JT, Burn DJ, Morris CM, Thomas AJ, Chinnery PF. Keogh MJ, et al. Transl Psychiatry. 2016 Feb 2;6(2):e728. doi: 10.1038/tp.2015.220. Transl Psychiatry. 2016. PMID: 26836416 Free PMC article.
53 results