Paisán-Ruíz C - Search Results

1

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.

Paisán-Ruíz C, Jain S, Evans EW, Gilks WP, Simón J, van der Brug M, López de Munain A, Aparicio S, Gil AM, Khan N, Johnson J, Martinez JR, Nicholl D, Martí Carrera I, Pena AS, de Silva R, Lees A, Martí-Massó JF, Pérez-Tur J, Wood NW, Singleton AB. Paisán-Ruíz C, et al. Neuron. 2004 Nov 18;44(4):595-600. doi: 10.1016/j.neuron.2004.10.023. Neuron. 2004. PMID: 15541308 Free article.

2

Familial Parkinson's disease: clinical and genetic analysis of four Basque families.

Paisàn-Ruìz C, Sàenz A, Lòpez de Munain A, Martì I, Martìnez Gil A, Martì-Massò JF, Pèrez-Tur J. Paisàn-Ruìz C, et al. Ann Neurol. 2005 Mar;57(3):365-72. doi: 10.1002/ana.20391. Ann Neurol. 2005. PMID: 15732106

3

Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques.

Simón-Sánchez J, Martí-Massó JF, Sánchez-Mut JV, Paisán-Ruiz C, Martínez-Gil A, Ruiz-Martínez J, Sáenz A, Singleton AB, López de Munain A, Pérez-Tur J. Simón-Sánchez J, et al. Mov Disord. 2006 Nov;21(11):1954-9. doi: 10.1002/mds.21114. Mov Disord. 2006. PMID: 16991141

4

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

Hernandez DG, Paisán-Ruíz C, McInerney-Leo A, Jain S, Meyer-Lindenberg A, Evans EW, Berman KF, Johnson J, Auburger G, Schäffer AA, Lopez GJ, Nussbaum RL, Singleton AB. Hernandez DG, et al. Ann Neurol. 2005 Mar;57(3):453-6. doi: 10.1002/ana.20401. Ann Neurol. 2005. PMID: 15732108

5

Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation.

Johnson J, Paisán-Ruíz C, Lopez G, Crews C, Britton A, Malkani R, Evans EW, McInerney-Leo A, Jain S, Nussbaum RL, Foote KD, Mandel RJ, Crawley A, Reimsnider S, Fernandez HH, Okun MS, Gwinn-Hardy K, Singleton AB. Johnson J, et al. Neurodegener Dis. 2007;4(5):386-91. doi: 10.1159/000105160. Epub 2007 Jul 6. Neurodegener Dis. 2007. PMID: 17622782

6

Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls.

Paisán-Ruíz C, Nath P, Washecka N, Gibbs JR, Singleton AB. Paisán-Ruíz C, et al. Hum Mutat. 2008 Apr;29(4):485-90. doi: 10.1002/humu.20668. Hum Mutat. 2008. PMID: 18213618

7

Parkinson's disease and low frequency alleles found together throughout LRRK2.

Paisán-Ruiz C, Washecka N, Nath P, Singleton AB, Corder EH. Paisán-Ruiz C, et al. Ann Hum Genet. 2009 Jul;73(Pt 4):391-403. doi: 10.1111/j.1469-1809.2009.00524.x. Epub 2009 May 21. Ann Hum Genet. 2009. PMID: 19489756 Free PMC article.

8

LRRK2: cause, risk, and mechanism.

Paisán-Ruiz C, Lewis PA, Singleton AB. Paisán-Ruiz C, et al. J Parkinsons Dis. 2013;3(2):85-103. doi: 10.3233/JPD-130192. J Parkinsons Dis. 2013. PMID: 23938341 Free PMC article. Review.

9

The genetics of Parkinson's syndromes: a critical review.

Hardy J, Lewis P, Revesz T, Lees A, Paisan-Ruiz C. Hardy J, et al. Curr Opin Genet Dev. 2009 Jun;19(3):254-65. doi: 10.1016/j.gde.2009.03.008. Epub 2009 May 4. Curr Opin Genet Dev. 2009. PMID: 19419854 Review.

10

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium.

Paisán-Ruíz C, Evans EW, Jain S, Xiromerisiou G, Gibbs JR, Eerola J, Gourbali V, Hellström O, Duckworth J, Papadimitriou A, Tienari PJ, Hadjigeorgiou GM, Singleton AB. Paisán-Ruíz C, et al. J Med Genet. 2006 Feb;43(2):e9. doi: 10.1136/jmg.2005.036889. J Med Genet. 2006. PMID: 16467219 Free PMC article.

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