Lincoln S - Search Results

1

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

Lockhart PJ, Lincoln S, Hulihan M, Kachergus J, Wilkes K, Bisceglio G, Mash DC, Farrer MJ. Lockhart PJ, et al. Among authors: lincoln s. J Med Genet. 2004 Mar;41(3):e22. doi: 10.1136/jmg.2003.011106. J Med Genet. 2004. PMID: 14985393 Free PMC article. No abstract available.

2

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.

Lockhart PJ, Bounds R, Hulihan M, Kachergus J, Lincoln S, Lin CH, Wu RM, Farrer MJ. Lockhart PJ, et al. Among authors: lincoln s. Mov Disord. 2004 Sep;19(9):1065-9. doi: 10.1002/mds.20082. Mov Disord. 2004. PMID: 15372597

3

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. Mov Disord. 2009 Jan 15;24(1):104-8. doi: 10.1002/mds.22093. Mov Disord. 2009. PMID: 19006224

4

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.

Mata IF, Alvarez V, Coto E, Blazquez M, Guisasola LM, Salvador C, Kachergus JM, Lincoln SJ, Farrer M. Mata IF, et al. Neurosci Lett. 2005 Jun 3;380(3):257-9. doi: 10.1016/j.neulet.2005.01.051. Epub 2005 Feb 8. Neurosci Lett. 2005. PMID: 15862897

5

Alpha-synuclein missense and multiplication mutations in autosomal dominant Parkinson's disease.

Hope AD, Myhre R, Kachergus J, Lincoln S, Bisceglio G, Hulihan M, Farrer MJ. Hope AD, et al. Among authors: lincoln s. Neurosci Lett. 2004 Aug 26;367(1):97-100. doi: 10.1016/j.neulet.2004.05.100. Neurosci Lett. 2004. PMID: 15308306

6

Identification of the human ubiquitin specific protease 31 (USP31) gene: structure, sequence and expression analysis.

Lockhart PJ, Hulihan M, Lincoln S, Hussey J, Skipper L, Bisceglio G, Wilkes K, Farrer MJ. Lockhart PJ, et al. Among authors: lincoln s. DNA Seq. 2004 Feb;15(1):9-14. doi: 10.1080/10855660310001638197. DNA Seq. 2004. PMID: 15354349

7

Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.

Wu RM, Bounds R, Lincoln S, Hulihan M, Lin CH, Hwu WL, Chen J, Gwinn-Hardy K, Farrer M. Wu RM, et al. Among authors: lincoln s. Arch Neurol. 2005 Jan;62(1):82-7. doi: 10.1001/archneur.62.1.82. Arch Neurol. 2005. PMID: 15642853

8

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: lincoln s. Neurology. 2004 Aug 10;63(3):550-3. doi: 10.1212/01.wnl.0000133402.78621.ad. Neurology. 2004. PMID: 15304593

9

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

Farrer M, Kachergus J, Forno L, Lincoln S, Wang DS, Hulihan M, Maraganore D, Gwinn-Hardy K, Wszolek Z, Dickson D, Langston JW. Farrer M, et al. Among authors: lincoln s. Ann Neurol. 2004 Feb;55(2):174-9. doi: 10.1002/ana.10846. Ann Neurol. 2004. PMID: 14755720

10

Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations.

Wiley J, Lynch T, Lincoln S, Skipper L, Hulihan M, Gosal D, Bisceglio G, Kachergus J, Hardy J, Farrer MJ. Wiley J, et al. Among authors: lincoln s. Mov Disord. 2004 Jun;19(6):677-81. doi: 10.1002/mds.10703. Mov Disord. 2004. PMID: 15197707

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