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Association studies in genetics
Citations 41-50 of 148 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Interactions of stroke, nonsteroidal anti-inflammatory drugs, and APOE status in dementia risk
- Joseph Rogers and Marwan N. Sabbagh
Neurology 2008; 70: 5-6.
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- VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
- Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104.
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- ARTICLES
Association of statin use with cognitive decline in elderly African Americans
- S. J. Szwast, H. C. Hendrie, K. A. Lane, S. Gao, S. E. Taylor, F. Unverzagt, J. Murrell, M. Deeg, A. Ogunniyi, M. R. Farlow, and K. S. Hall
Neurology 2007; 69: 1873-1880.
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- ARTICLES
 -Synuclein and Parkinson disease susceptibility
- S. Winkler, J. Hagenah, S. Lincoln, M. Heckman, K. Haugarvoll, K. Lohmann-Hedrich, V. Kostic, M. Farrer, and C. Klein
Neurology 2007; 69: 1745-1750.
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- ARTICLES
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: Is there a gender effect?
- A. Orr-Urtreger, C. Shifrin, U. Rozovski, S. Rosner, D. Bercovich, T. Gurevich, H. Yagev-More, A. Bar-Shira, and N. Giladi
Neurology 2007; 69: 1595-1602.
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- ARTICLES
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
- L. N. Clark, B. M. Ross, Y. Wang, H. Mejia-Santana, J. Harris, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, R. Ottman, and K. Marder
Neurology 2007; 69: 1270-1277.
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- ARTICLES
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease
- P. T. Luoma, J. Eerola, S. Ahola, A. H. Hakonen, O. Hellström, K. T. Kivistö, P. J. Tienari, and A. Suomalainen
Neurology 2007; 69: 1152-1159.
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- ARTICLES
Inherited prion disease with 5-OPRI: Phenotype modification by repeat length and codon 129
- S. Mead, T. E. F. Webb, T. A. Campbell, J. Beck, J. M. Linehan, S. Rutherfoord, S. Joiner, J. D. F. Wadsworth, J. Heckmann, S. Wroe, L. Doey, A. King, and J. Collinge
Neurology 2007; 69: 730-738.
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- ARTICLES
Meta-analysis of APOE genotype and subarachnoid hemorrhage: Clinical outcome and delayed ischemia
- L. A. Lanterna, Y. Ruigrok, S. Alexander, J. Tang, F. Biroli, L. T. Dunn, and W. S. Poon
Neurology 2007; 69: 766-775.
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- ARTICLES
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
- A. Di Fonzo, H. F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, G. Abbruzzese, P. Marini, F. Squitieri, M. W. Horstink, P. Montagna, A. Dalla Libera, F. Stocchi, S. Goldwurm, J. J. Ferreira, G. Meco, E. Martignoni, L. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, The Italian Parkinson Genetics Network, and V. Bonifati
Neurology 2007; 68: 1557-1562.
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