Farrer MJ - Search Results

1

Genealogical studies in LRRK2-associated Parkinson's disease in central Norway.

Johansen KK, Hasselberg K, White LR, Farrer MJ, Aasly JO. Johansen KK, et al. Among authors: farrer mj. Parkinsonism Relat Disord. 2010 Sep;16(8):527-30. doi: 10.1016/j.parkreldis.2010.05.005. Epub 2010 Jul 10. Parkinsonism Relat Disord. 2010. PMID: 20621541

2

The tau H1 haplotype is associated with Parkinson's disease in the Norwegian population.

Farrer M, Skipper L, Berg M, Bisceglio G, Hanson M, Hardy J, Adam A, Gwinn-Hardy K, Aasly J. Farrer M, et al. Neurosci Lett. 2002 Apr 5;322(2):83-6. doi: 10.1016/s0304-3940(02)00106-4. Neurosci Lett. 2002. PMID: 11958849

3

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. 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.

4

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

5

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.

6

Clinical features of LRRK2-associated Parkinson's disease in central Norway.

Aasly JO, Toft M, Fernandez-Mata I, Kachergus J, Hulihan M, White LR, Farrer M. Aasly JO, et al. Ann Neurol. 2005 May;57(5):762-5. doi: 10.1002/ana.20456. Ann Neurol. 2005. PMID: 15852371

7

LRRK2 R1441G in Spanish patients with Parkinson's disease.

Mata IF, Taylor JP, Kachergus J, Hulihan M, Huerta C, Lahoz C, Blazquez M, Guisasola LM, Salvador C, Ribacoba R, Martinez C, Farrer M, Alvarez V. Mata IF, et al. Neurosci Lett. 2005 Jul 15;382(3):309-11. doi: 10.1016/j.neulet.2005.03.033. Epub 2005 Apr 13. Neurosci Lett. 2005. PMID: 15925109

8

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

9

Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.

Gosal D, Ross OA, Wiley J, Irvine GB, Johnston JA, Toft M, Mata IF, Kachergus J, Hulihan M, Taylor JP, Lincoln SJ, Farrer MJ, Lynch T, Mark Gibson J. Gosal D, et al. Among authors: farrer mj. Parkinsonism Relat Disord. 2005 Sep;11(6):349-52. doi: 10.1016/j.parkreldis.2005.05.004. Parkinsonism Relat Disord. 2005. PMID: 16102999

10

LRRK2 mutations in Parkinson disease.

Farrer M, Stone J, Mata IF, Lincoln S, Kachergus J, Hulihan M, Strain KJ, Maraganore DM. Farrer M, et al. Neurology. 2005 Sep 13;65(5):738-40. doi: 10.1212/01.wnl.0000169023.51764.b0. Neurology. 2005. PMID: 16157908

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