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Is the MC1R variant p.R160W associated with Parkinson's?
Lubbe SJ, Escott-Price V, Brice A, Gasser T, Hardy J, Heutink P, Sharma M, Wood NW, Nalls M, Singleton AB, Williams NM, Morris HR; International Parkinson's Disease Genomics Consortium. Lubbe SJ, et al. Among authors: williams nm. Ann Neurol. 2016 Jan;79(1):159-61. doi: 10.1002/ana.24527. Epub 2015 Dec 12. Ann Neurol. 2016. PMID: 26389967 Free PMC article. No abstract available.
Case control analysis of repeat expansion size in ataxia.
Majounie E, Wardle M, Muzaimi M, Cross WC, Robertson NP, Williams NM, Morris HR. Majounie E, et al. Among authors: williams nm. Neurosci Lett. 2007 Dec 11;429(1):28-32. doi: 10.1016/j.neulet.2007.09.055. Epub 2007 Oct 2. Neurosci Lett. 2007. PMID: 17961920
Dentatorubral pallidoluysian atrophy in South Wales.
Wardle M, Majounie E, Williams NM, Rosser AE, Morris HR, Robertson NP. Wardle M, et al. Among authors: williams nm. J Neurol Neurosurg Psychiatry. 2008 Jul;79(7):804-7. doi: 10.1136/jnnp.2007.128074. Epub 2007 Oct 26. J Neurol Neurosurg Psychiatry. 2008. PMID: 17965145
Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
Wickremaratchi MM, Majounie E, Morris HR, Williams NM, Lewis H, Gill SS, Khan S, Heywood P, Hardy J, Wiles CM, Singleton AB, Quinn NP. Wickremaratchi MM, et al. Among authors: williams nm. Mov Disord. 2009 Jan 15;24(1):138-40. doi: 10.1002/mds.22181. Mov Disord. 2009. PMID: 18942080 Free PMC article. Review. No abstract available.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Hölttä-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chiò A, Restagno G, Borghero G, Sabatelli M; ITALSGEN Consortium; Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ. Renton AE, et al. Among authors: williams nm. Neuron. 2011 Oct 20;72(2):257-68. doi: 10.1016/j.neuron.2011.09.010. Epub 2011 Sep 21. Neuron. 2011. PMID: 21944779 Free PMC article.
Recent advances in the genetics of the ALS-FTLD complex.
Morris HR, Waite AJ, Williams NM, Neal JW, Blake DJ. Morris HR, et al. Among authors: williams nm. Curr Neurol Neurosci Rep. 2012 Jun;12(3):243-50. doi: 10.1007/s11910-012-0268-5. Curr Neurol Neurosci Rep. 2012. PMID: 22477152 Review.
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
Kilarski LL, Pearson JP, Newsway V, Majounie E, Knipe MD, Misbahuddin A, Chinnery PF, Burn DJ, Clarke CE, Marion MH, Lewthwaite AJ, Nicholl DJ, Wood NW, Morrison KE, Williams-Gray CH, Evans JR, Sawcer SJ, Barker RA, Wickremaratchi MM, Ben-Shlomo Y, Williams NM, Morris HR. Kilarski LL, et al. Among authors: williams gray ch, williams nm. Mov Disord. 2012 Oct;27(12):1522-9. doi: 10.1002/mds.25132. Epub 2012 Sep 6. Mov Disord. 2012. PMID: 22956510 Review.
345 results