Farrer MJ - Search Results

1

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

Lee MJ, Mata IF, Lin CH, Tzen KY, Lincoln SJ, Bounds R, Lockhart PJ, Hulihan MM, Farrer MJ, Wu RM. Lee MJ, et al. Among authors: farrer mj. Mov Disord. 2009 Jan 15;24(1):104-8. doi: 10.1002/mds.22093. Mov Disord. 2009. PMID: 19006224

2

Linkage exclusion in French families with probable Parkinson' s disease.

Farrer M, Destée T, Becquet E, Wavrant-De Vrièze F, Mouroux V, Richard F, Defebvre L, Lincoln S, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Mov Disord. 2000 Nov;15(6):1075-83. doi: 10.1002/1531-8257(200011)15:6<1075::aid-mds1004>3.0.co;2-2. Mov Disord. 2000. PMID: 11104189

3

Identification and characterization of the human parkin gene promoter.

West A, Farrer M, Petrucelli L, Cookson M, Lockhart P, Hardy J. West A, et al. J Neurochem. 2001 Sep;78(5):1146-52. doi: 10.1046/j.1471-4159.2001.00512.x. J Neurochem. 2001. PMID: 11553688 Free article.

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

The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3.

Lockhart PJ, Holtom B, Lincoln S, Hussey J, Zimprich A, Gasser T, Wszolek ZK, Hardy J, Farrer MJ. Lockhart PJ, et al. Among authors: farrer mj. Gene. 2002 Feb 20;285(1-2):229-37. doi: 10.1016/s0378-1119(02)00402-x. Gene. 2002. PMID: 12039050

6

Complex relationship between Parkin mutations and Parkinson disease.

West A, Periquet M, Lincoln S, Lücking CB, Nicholl D, Bonifati V, Rawal N, Gasser T, Lohmann E, Deleuze JF, Maraganore D, Levey A, Wood N, Dürr A, Hardy J, Brice A, Farrer M; French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility on Parkinson's Disease. West A, et al. Am J Med Genet. 2002 Jul 8;114(5):584-91. doi: 10.1002/ajmg.10525. Am J Med Genet. 2002. PMID: 12116199

7

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.

Wu RM, Shan DE, Sun CM, Liu RS, Hwu WL, Tai CH, Hussey J, West A, Gwinn-Hardy K, Hardy J, Chen J, Farrer M, Lincoln S. Wu RM, et al. Mov Disord. 2002 Jul;17(4):670-5. doi: 10.1002/mds.10184. Mov Disord. 2002. PMID: 12210855

8

Functional association of the parkin gene promoter with idiopathic Parkinson's disease.

West AB, Maraganore D, Crook J, Lesnick T, Lockhart PJ, Wilkes KM, Kapatos G, Hardy JA, Farrer MJ. West AB, et al. Among authors: farrer mj. Hum Mol Genet. 2002 Oct 15;11(22):2787-92. doi: 10.1093/hmg/11.22.2787. Hum Mol Genet. 2002. PMID: 12374768

9

Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.

Hussey J, Lockhart PJ, Seltzer W, Wszolek ZK, Payami H, Hanson M, Gwinn-Hardy K, Farrer M. Hussey J, et al. Genet Test. 2002 Fall;6(3):217-20. doi: 10.1089/109065702761403397. Genet Test. 2002. PMID: 12490063

10

Identification of a novel gene linked to parkin via a bi-directional promoter.

West AB, Lockhart PJ, O'Farell C, Farrer MJ. West AB, et al. Among authors: farrer mj. J Mol Biol. 2003 Feb 7;326(1):11-9. doi: 10.1016/s0022-2836(02)01376-1. J Mol Biol. 2003. PMID: 12547187

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

451 results

Search Page