Lincoln S - Search Results

1

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.

Allen M, Kachadoorian M, Quicksall Z, Zou F, Chai HS, Younkin C, Crook JE, Pankratz VS, Carrasquillo MM, Krishnan S, Nguyen T, Ma L, Malphrus K, Lincoln S, Bisceglio G, Kolbert CP, Jen J, Mukherjee S, Kauwe JK, Crane PK, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Schellenberg GD, Parisi JE, Petersen RC, Graff-Radford NR, Dickson DW, Younkin SG, Ertekin-Taner N. Allen M, et al. Among authors: lincoln s. Alzheimers Res Ther. 2014 Jul 1;6(4):39. doi: 10.1186/alzrt268. eCollection 2014. Alzheimers Res Ther. 2014. PMID: 25324900 Free PMC article.

2

Pathology of PD in monozygotic twins with a 20-year discordance interval.

Dickson D, Farrer M, Lincoln S, Mason RP, Zimmerman TR Jr, Golbe LI, Hardy J. Dickson D, et al. Among authors: lincoln s. Neurology. 2001 Apr 10;56(7):981-2. doi: 10.1212/wnl.56.7.981. Neurology. 2001. PMID: 11294946 No abstract available.

3

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

4

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

5

Biochemical characterization of torsinB.

O'Farrell C, Lockhart PJ, Lincoln S, De Lucia M, Singleton AB, Dickson DW, Cookson MR. O'Farrell C, et al. Among authors: lincoln s. Brain Res Mol Brain Res. 2004 Aug 23;127(1-2):1-9. doi: 10.1016/j.molbrainres.2004.05.005. Brain Res Mol Brain Res. 2004. PMID: 15306116

6

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

7

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

8

Multiplication of the alpha-synuclein gene is not a common disease mechanism in Lewy body disease.

Lockhart PJ, Kachergus J, Lincoln S, Hulihan M, Bisceglio G, Thomas N, Dickson D, Farrer MJ. Lockhart PJ, et al. Among authors: lincoln s. J Mol Neurosci. 2004;24(3):337-42. doi: 10.1385/JMN:24:3:337. J Mol Neurosci. 2004. PMID: 15655258

9

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: lincoln sj. Neuropathol Appl Neurobiol. 2006 Feb;32(1):23-5. doi: 10.1111/j.1365-2990.2006.00693.x. Neuropathol Appl Neurobiol. 2006. PMID: 16409550

10

Anatomical localization of leucine-rich repeat kinase 2 in mouse brain.

Melrose H, Lincoln S, Tyndall G, Dickson D, Farrer M. Melrose H, et al. Among authors: lincoln s. Neuroscience. 2006;139(3):791-4. doi: 10.1016/j.neuroscience.2006.01.017. Epub 2006 Feb 28. Neuroscience. 2006. PMID: 16504409

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