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Page 1
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
Gallagher MD, Suh E, Grossman M, Elman L, McCluskey L, Van Swieten JC, Al-Sarraj S, Neumann M, Gelpi E, Ghetti B, Rohrer JD, Halliday G, Van Broeckhoven C, Seilhean D, Shaw PJ, Frosch MP, Alafuzoff I, Antonell A, Bogdanovic N, Brooks W, Cairns NJ, Cooper-Knock J, Cotman C, Cras P, Cruts M, De Deyn PP, DeCarli C, Dobson-Stone C, Engelborghs S, Fox N, Galasko D, Gearing M, Gijselinck I, Grafman J, Hartikainen P, Hatanpaa KJ, Highley JR, Hodges J, Hulette C, Ince PG, Jin LW, Kirby J, Kofler J, Kril J, Kwok JB, Levey A, Lieberman A, Llado A, Martin JJ, Masliah E, McDermott CJ, McKee A, McLean C, Mead S, Miller CA, Miller J, Munoz DG, Murrell J, Paulson H, Piguet O, Rossor M, Sanchez-Valle R, Sano M, Schneider J, Silbert LC, Spina S, van der Zee J, Van Langenhove T, Warren J, Wharton SB, White CL 3rd, Woltjer RL, Trojanowski JQ, Lee VM, Van Deerlin V, Chen-Plotkin AS. Gallagher MD, et al. Among authors: brooks w. Acta Neuropathol. 2014 Mar;127(3):407-18. doi: 10.1007/s00401-013-1239-x. Epub 2014 Jan 19. Acta Neuropathol. 2014. PMID: 24442578 Free PMC article.
Identification of families with cortical Lewy body disease.
Harding AJ, Das A, Kril JJ, Brooks WS, Duffy D, Halliday GM. Harding AJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):118-22. doi: 10.1002/ajmg.b.30014. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211643
Similar early clinical presentations in familial and non-familial frontotemporal dementia.
Piguet O, Brooks WS, Halliday GM, Schofield PR, Stanford PM, Kwok JB, Spillantini MG, Yancopoulou D, Nestor PJ, Broe GA, Hodges JR. Piguet O, et al. Among authors: brooks ws. J Neurol Neurosurg Psychiatry. 2004 Dec;75(12):1743-5. doi: 10.1136/jnnp.2003.031948. J Neurol Neurosurg Psychiatry. 2004. PMID: 15548495 Free PMC article.
Neuropathology in the S305S tau gene mutation.
Halliday GM, Song YJ, Creasey H, Morris JG, Brooks WS, Kril JJ. Halliday GM, et al. Brain. 2006 Mar;129(Pt 3):E40. doi: 10.1093/brain/awh720. Brain. 2006. PMID: 16477083 No abstract available.
Mutations in progranulin explain atypical phenotypes with variants in MAPT.
Pickering-Brown SM, Baker M, Gass J, Boeve BF, Loy CT, Brooks WS, Mackenzie IR, Martins RN, Kwok JB, Halliday GM, Kril J, Schofield PR, Mann DM, Hutton M. Pickering-Brown SM, et al. Brain. 2006 Nov;129(Pt 11):3124-6. doi: 10.1093/brain/awl289. Brain. 2006. PMID: 17071927
1,342 results