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Page 1
Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
Skipper L, Wilkes K, Toft M, Baker M, Lincoln S, Hulihan M, Ross OA, Hutton M, Aasly J, Farrer M. Skipper L, et al. Among authors: farrer m. Am J Hum Genet. 2004 Oct;75(4):669-77. doi: 10.1086/424492. Epub 2004 Aug 3. Am J Hum Genet. 2004. PMID: 15297935 Free PMC article.
Parkinsonism, FXTAS, and FMR1 premutations.
Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ. Toft M, et al. Among authors: farrer mj. Mov Disord. 2005 Feb;20(2):230-3. doi: 10.1002/mds.20297. Mov Disord. 2005. PMID: 15390127
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M. Kachergus J, et al. Among authors: farrer mj. Am J Hum Genet. 2005 Apr;76(4):672-80. doi: 10.1086/429256. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726496 Free PMC article.
LRRK2 mutations and Parkinsonism.
Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ. Toft M, et al. Among authors: farrer mj. Lancet. 2005 Apr 2-8;365(9466):1229-30. doi: 10.1016/S0140-6736(05)74809-1. Lancet. 2005. PMID: 15811454 No abstract available.
LRRK2 mutations are not common in Alzheimer's disease.
Toft M, Sando SB, Melquist S, Ross OA, White LR, Aasly JO, Farrer MJ. Toft M, et al. Among authors: farrer mj. Mech Ageing Dev. 2005 Nov;126(11):1201-5. doi: 10.1016/j.mad.2005.06.010. Mech Ageing Dev. 2005. PMID: 16087219
Lrrk2 R1441 substitution and progressive supranuclear palsy.
Ross OA, Whittle AJ, Cobb SA, Hulihan MM, Lincoln SJ, Toft M, Farrer MJ, Dickson DW. Ross OA, et al. Among authors: farrer mj. Neuropathol Appl Neurobiol. 2006 Feb;32(1):23-5. doi: 10.1111/j.1365-2990.2006.00693.x. Neuropathol Appl Neurobiol. 2006. PMID: 16409550
482 results