Farrer MJ - Search Results

1

Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population.

Toft M, Pielsticker L, Ross OA, Aasly JO, Farrer MJ. Toft M, et al. Among authors: farrer mj. Neurology. 2006 Feb 14;66(3):415-7. doi: 10.1212/01.wnl.0000196492.80676.7c. Neurology. 2006. PMID: 16476943

2

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Farrer M, et al. Ann Neurol. 1998 Mar;43(3):394-7. doi: 10.1002/ana.410430320. Ann Neurol. 1998. PMID: 9506559

3

Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease.

Maraganore DM, Farrer MJ, Hardy JA, Lincoln SJ, McDonnell SK, Rocca WA. Maraganore DM, et al. Among authors: farrer mj. Neurology. 1999 Nov 10;53(8):1858-60. doi: 10.1212/wnl.53.8.1858. Neurology. 1999. PMID: 10563640

4

Lewy bodies and parkinsonism in families with parkin mutations.

Farrer M, Chan P, Chen R, Tan L, Lincoln S, Hernandez D, Forno L, Gwinn-Hardy K, Petrucelli L, Hussey J, Singleton A, Tanner C, Hardy J, Langston JW. Farrer M, et al. Ann Neurol. 2001 Sep;50(3):293-300. doi: 10.1002/ana.1132. Ann Neurol. 2001. PMID: 11558785

5

Case-Control study of the extended tau gene haplotype in Parkinson's disease.

Maraganore DM, Hernandez DG, Singleton AB, Farrer MJ, McDonnell SK, Hutton ML, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: farrer mj. Ann Neurol. 2001 Nov;50(5):658-61. doi: 10.1002/ana.1228. Ann Neurol. 2001. PMID: 11706972

6

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

7

Parkin-proven disease: common founders but divergent phenotypes.

Lincoln S, Wiley J, Lynch T, Langston JW, Chen R, Lang A, Rogaeva E, Sa DS, Munhoz RP, Harris J, Marder K, Klein C, Bisceglio G, Hussey J, West A, Hulihan M, Hardy J, Farrer M. Lincoln S, et al. Neurology. 2003 May 27;60(10):1605-10. doi: 10.1212/01.wnl.0000064289.49410.a9. Neurology. 2003. PMID: 12771249

8

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.

9

A limited role for DJ1 in Parkinson disease susceptibility.

Maraganore DM, Wilkes K, Lesnick TG, Strain KJ, de Andrade M, Rocca WA, Bower JH, Ahlskog JE, Lincoln S, Farrer MJ. Maraganore DM, et al. Among authors: farrer mj. Neurology. 2004 Aug 10;63(3):550-3. doi: 10.1212/01.wnl.0000133402.78621.ad. Neurology. 2004. PMID: 15304593

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

449 results

Search Page