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Association studies in genetics
Citations 51-60 of 147 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Comprehensive association analysis of the NOS2A gene with Parkinson disease
- C. Schulte, M. Sharma, J. C. Mueller, P. Lichtner, J. Prestel, D. Berg, and T. Gasser
Neurology 2006; 67: 2080-2082.
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- BRIEF COMMUNICATIONS
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura
- U. Todt, J. Freudenberg, I. Goebel, A. Heinze, K. Heinze-Kuhn, M. Rietschel, H. Göbel, and C. Kubisch
Neurology 2006; 67: 1707-1709.
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- EDITORIALS
Susceptibility genes in sporadic ALS: Separating the wheat from the chaff by international collaboration
- Christopher E. Shaw and Ammar Al-Chalabi
Neurology 2006; 67: 738-739.
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- ARTICLES
Paraoxonase gene polymorphisms and sporadic ALS
- A. Slowik, B. Tomik, P. P. Wolkow, D. Partyka, W. Turaj, M. T. Malecki, J. Pera, T. Dziedzic, A. Szczudlik, and D. A. Figlewicz
Neurology 2006; 67: 766-770.
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- ARTICLES
Paraoxonase cluster polymorphisms are associated with sporadic ALS
- M. Saeed, N. Siddique, W. Y. Hung, E. Usacheva, E. Liu, R. L. Sufit, S. L. Heller, J. L. Haines, M. Pericak-Vance, and T. Siddique
Neurology 2006; 67: 771-776.
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- BRIEF COMMUNICATIONS
Polymorphism in Sp1 recognition site of the EGF receptor gene promoter and risk of glioblastoma
- C. Carpentier, F. Laigle-Donadey, Y. Marie, N. Auger, A. Benouaich-Amiel, J. Lejeune, G. Kaloshi, J. -Y. Delattre, J. Thillet, and M. Sanson
Neurology 2006; 67: 872-874.
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- BRIEF COMMUNICATIONS
Lack of association of VEGF promoter polymorphisms with sporadic ALS
- W. Chen, M. Saeed, H. Mao, N. Siddique, L. Dellefave, W. -Y. Hung, H. -X. Deng, R. L. Sufit, S. L. Heller, J. L. Haines, M. Pericak-Vance, and T. Siddique
Neurology 2006; 67: 508-510.
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- BRIEF COMMUNICATIONS
The effect of APOE genotype on clinical phenotype in Alzheimer disease
- W. M. van der Flier, S.N.M. Schoonenboom, Y. A.L. Pijnenburg, N. C. Fox, and P. Scheltens
Neurology 2006; 67: 526-527.
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- BRIEF COMMUNICATIONS
Cluster headache is associated with the G1246A polymorphism in the hypocretin receptor 2 gene
- M. Schürks, T. Kurth, I. Geissler, G. Tessmann, H. -C. Diener, and D. Rosskopf
Neurology 2006; 66: 1917-1919.
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- BRIEF COMMUNICATIONS
Dysphagia in facioscapulohumeral muscular dystrophy
- M. Wohlgemuth, B.J.M. de Swart, J. G. Kalf, F. B.M. Joosten, A. M. Van der Vliet, and G. W. Padberg
Neurology 2006; 66: 1926-1928.
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