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An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation.
Witherden AS, Hafezparast M, Nicholson SJ, Ahmad-Annuar A, Bermingham N, Arac D, Rankin J, Iravani M, Ball S, Peters J, Martin JE, Huntley D, Hummerich H, Sergot M, Fisher EM. Witherden AS, et al. Gene. 2002 Jan 23;283(1-2):71-82. doi: 10.1016/s0378-1119(01)00853-8. Gene. 2002. PMID: 11867214
Mutations in dynein link motor neuron degeneration to defects in retrograde transport.
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, Ball S, Peters J, Toda T, Yamamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickneite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schlegel J, Fuchs H, Hrabe de Angelis M, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EM. Hafezparast M, et al. Science. 2003 May 2;300(5620):808-12. doi: 10.1126/science.1083129. Science. 2003. PMID: 12730604
Mouse models for neurological disease.
Hafezparast M, Ahmad-Annuar A, Wood NW, Tabrizi SJ, Fisher EM. Hafezparast M, et al. Lancet Neurol. 2002 Aug;1(4):215-24. doi: 10.1016/s1474-4422(02)00100-x. Lancet Neurol. 2002. PMID: 12849454 Review.
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.
Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, Fisher EM. Ahmad-Annuar A, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):150-7. doi: 10.1080/14660820310011737. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129801
Paradigms for the identification of new genes in motor neuron degeneration.
Hafezparast M, Ahmad-Annuar A, Hummerich H, Shah P, Ford M, Baker C, Bowen S, Martin JE, Fisher EM. Hafezparast M, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Dec;4(4):249-57. doi: 10.1080/14660820310016084. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 14753659
Association of HLA locus variant in Parkinson's disease.
Zhao Y, Gopalai AA, Ahmad-Annuar A, Teng EW, Prakash KM, Tan LC, Au WL, Li HH, Lim SY, Lim SK, Chong YB, Tan LP, Ibrahim NM, Tan EK. Zhao Y, et al. Clin Genet. 2013 Nov;84(5):501-4. doi: 10.1111/cge.12024. Epub 2012 Oct 29. Clin Genet. 2013. PMID: 23083294
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.
Gopalai AA, Lim SY, Chua JY, Tey S, Lim TT, Mohamed Ibrahim N, Tan AH, Eow GB, Abdul Aziz Z, Puvanarajah SD, Viswanathan S, Looi I, Lim SK, Tan LP, Chong YB, Tan CT, Zhao Y, Tan EK, Ahmad-Annuar A. Gopalai AA, et al. Biomed Res Int. 2014;2014:867321. doi: 10.1155/2014/867321. Epub 2014 Aug 28. Biomed Res Int. 2014. PMID: 25243190 Free PMC article.
PARK16 is associated with PD in the Malaysian population.
Gopalai AA, Ahmad-Annuar A, Li HH, Zhao Y, Lim SY, Tan AH, Lim TT, Eow GB, Santhi P, Shanthi V, Norlinah MI, Aziz ZA, Lim SK, Tan CT, Tan EK. Gopalai AA, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):839-47. doi: 10.1002/ajmg.b.32454. Epub 2016 May 13. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27174169
68 results