Kachergus J - Search Results

1

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: kachergus j. Mov Disord. 2004 Sep;19(9):1065-9. doi: 10.1002/mds.20082. Mov Disord. 2004. PMID: 15372597

2

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: kachergus j. Mov Disord. 2004 Jun;19(6):677-81. doi: 10.1002/mds.10703. Mov Disord. 2004. PMID: 15197707

3

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.

Toft M, Mata IF, Ross OA, Kachergus J, Hulihan MM, Haugarvoll K, Stone JT, Blazquez M, Gibson JM, Aasly JO, White LR, Lynch T, Adler CH, Gwinn-Hardy K, Farrer MJ. Toft M, et al. Among authors: kachergus j. Mov Disord. 2007 Feb 15;22(3):389-92. doi: 10.1002/mds.21217. Mov Disord. 2007. PMID: 17216639

4

LRRK2 variation and Parkinson's disease in African Americans.

Ross OA, Wilhoite GJ, Bacon JA, Soto-Ortolaza A, Kachergus J, Cobb SA, Puschmann A, Vilariño-Güell C, Farrer MJ, Graff-Radford N, Meschia JF, Wszolek ZK. Ross OA, et al. Among authors: kachergus j. Mov Disord. 2010 Sep 15;25(12):1973-6. doi: 10.1002/mds.23163. Mov Disord. 2010. PMID: 20669299 Free PMC article.

5

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. Among authors: kachergus jm. 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

6

Lrrk2 pathogenic substitutions in Parkinson's disease.

Mata IF, Kachergus JM, Taylor JP, Lincoln S, Aasly J, Lynch T, Hulihan MM, Cobb SA, Wu RM, Lu CS, Lahoz C, Wszolek ZK, Farrer MJ. Mata IF, et al. Among authors: kachergus jm. Neurogenetics. 2005 Dec;6(4):171-7. doi: 10.1007/s10048-005-0005-1. Epub 2005 Sep 17. Neurogenetics. 2005. PMID: 16172858

7

Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease.

Taylor JP, Hulihan MM, Kachergus JM, Melrose HL, Lincoln SJ, Hinkle KM, Stone JT, Ross OA, Hauser R, Aasly J, Gasser T, Payami H, Wszolek ZK, Farrer MJ. Taylor JP, et al. Among authors: kachergus jm. Neurogenetics. 2007 Apr;8(2):95-102. doi: 10.1007/s10048-006-0075-8. Epub 2007 Jan 16. Neurogenetics. 2007. PMID: 17225181

8

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.

Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Hentati E, Hentati F, Farrer MJ. Nishioka K, et al. Among authors: kachergus jm. Parkinsonism Relat Disord. 2010 Dec;16(10):686-7. doi: 10.1016/j.parkreldis.2010.09.007. Epub 2010 Oct 23. Parkinsonism Relat Disord. 2010. PMID: 20971673 Free PMC article.

9

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: kachergus j. Neurosci Lett. 2004 Aug 26;367(1):97-100. doi: 10.1016/j.neulet.2004.05.100. Neurosci Lett. 2004. PMID: 15308306

10

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: kachergus j. J Mol Neurosci. 2004;24(3):337-42. doi: 10.1385/JMN:24:3:337. J Mol Neurosci. 2004. PMID: 15655258

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