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Association studies in genetics
Citations 91-100 of 148 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
DD genotype of ACE gene is a risk factor for intracerebral hemorrhage
- A. Slowik, W. Turaj, T. Dziedzic, A. Haefele, J. Pera, M. T. Malecki, L. Glodzik-Sobanska, P. Szermer, D. A. Figlewicz, and A. Szczudlik
Neurology 2004; 63: 359-361.
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- BRIEF COMMUNICATIONS
Prion protein codon 129 polymorphism and risk of Alzheimer disease
- M. Riemenschneider, N. Klopp, W. Xiang, S. Wagenpfeil, C. Vollmert, U. Müller, H. Förstl, T. Illig, H. Kretzschmar, and A. Kurz
Neurology 2004; 63: 364-366.
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- BRIEF COMMUNICATIONS
Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population
- S. Helisalmi, B. Dermaut, M. Hiltunen, A. Mannermaa, M. Van den Broeck, M. Lehtovirta, A. M. Koivisto, S. Iivonen, M. Cruts, H. Soininen, and C. Van Broeckhoven
Neurology 2004; 63: 173-175.
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- ARTICLES
APOE- 2 allele associated with higher prevalence of sporadic Parkinson disease
- Xuemei Huang, Peter C. Chen, and Charles Poole
Neurology 2004; 62: 2198-2202.
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- BRIEF COMMUNICATIONS
Susceptibility and outcome in MS: Associations with polymorphisms in pigmentation-related genes
- J. M. Partridge, S. J.M. Weatherby, J. A. Woolmore, D. J. Highland, A. A. Fryer, C. L.A. Mann, M. D. Boggild, W. E.R. Ollier, R. C. Strange, and C. P. Hawkins
Neurology 2004; 62: 2323-2325.
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- ARTICLES
Impact of APOE genotype on neuropathologic and neurochemical markers of Alzheimer disease
- P. Tiraboschi, L. A. Hansen, E. Masliah, M. Alford, L. J. Thal, and J. Corey-Bloom
Neurology 2004; 62: 1977-1983.
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- BRIEF COMMUNICATIONS
APOE 4 allele is associated with reduced cerebrospinal fluid levels of Aß42
- J. A. Prince, H. Zetterberg, N. Andreasen, J. Marcusson, and K. Blennow
Neurology 2004; 62: 2116-2118.
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- CLINICAL/SCIENTIFIC NOTES
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
- P. Ibáñez, E. Lohmann, P. Pollak, F. Durif, C. Tranchant, Y. Agid, A. Dürr, and A. Brice
Neurology 2004; 62: 2133-2134.
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- CLINICAL/SCIENTIFIC NOTES
Glutathione transferase Omega class polymorphisms in Parkinson disease
- A. K. Whitbread, G. D. Mellick, P. A. Silburn, D. G. Le Couteur, and P. G. Board
Neurology 2004; 62: 1910-1911.
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- BRIEF COMMUNICATIONS
HFE mutations are not strongly associated with sporadic ALS
- A. A. Yen, E. P. Simpson, J. S. Henkel, D. R. Beers, and S. H. Appel
Neurology 2004; 62: 1611-1612.
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