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Association studies in genetics
Citations 1-10 of 124 total displayed.
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Most recent content
(7 Oct 2008):
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- ARTICLES
Progranulin variability has no major role in Parkinson disease genetic etiology
- K. Nuytemans, P. Pals, K. Sleegers, S. Engelborghs, E. Corsmit, K. Peeters, B. Pickut, M. Mattheijssens, P. Cras, P. P. De Deyn, J. Theuns, and C. Van Broeckhoven
Neurology 2008; 71: 1147-1151.
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Past content
(since Jan 2001):
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- ARTICLES
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
- N. Brouwers, K. Sleegers, S. Engelborghs, S. Maurer-Stroh, I. Gijselinck, J. van der Zee, B. A. Pickut, M. Van den Broeck, M. Mattheijssens, K. Peeters, J. Schymkowitz, F. Rousseau, J. -J. Martin, M. Cruts, P. P. De Deyn, and C. Van Broeckhoven
Neurology 2008; 71: 656-664.
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- ARTICLES
Melanocortin 1 receptor genotype, past environmental sun exposure, and risk of multiple sclerosis
- T. Dwyer, I. van der Mei, A-L Ponsonby, B. V. Taylor, J. Stankovich, J. D. McKay, R. J. Thomson, A. M. Polanowski, and J. L. Dickinson
Neurology 2008; 71: 583-589.
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- ARTICLES
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden
- P. N. Valdmanis, E. Kabashi, A. Dyck, P. Hince, J. Lee, P. Dion, M. D'Amour, F. Souchon, J. -P. Bouchard, F. Salachas, V. Meininger, P. M. Andersen, W. Camu, N. Dupré, and G. A. Rouleau
Neurology 2008; 71: 514-520.
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- ARTICLES
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
- K. Sleegers, N. Brouwers, S. Maurer-Stroh, M. A. van Es, P. Van Damme, P.W.J. van Vught, J. van der Zee, S. Serneels, T. De Pooter, M. Van den Broeck, M. Cruts, J. Schymkowitz, P. De Jonghe, F. Rousseau, L. H. van den Berg, W. Robberecht, and C. Van Broeckhoven
Neurology 2008; 71: 253-259.
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- ARTICLES
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, and T. Sander
Neurology 2008; 71: 177-183.
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- CLINICAL/SCIENTIFIC NOTES
Celiac antibodies in the diagnostic workup of white matter lesions
- F. Paul, C. F. Pfueller, J. T. Wuerfel, K. Egerer, B. Tanczos, D. C. Baumgart, and F. Zipp
Neurology 2008; 71: 223-225.
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- EDITORIALS
Association, expression, pathobiology: Is too much tau in PD a blueprint for genetic association?
- Andrew Singleton and Huw Morris
Neurology 2008; 71: 11-12.
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- ARTICLES
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
- J. E. Tobin, J. C. Latourelle, M. F. Lew, C. Klein, O. Suchowersky, H. A. Shill, L. I. Golbe, M. H. Mark, J. H. Growdon, G. F. Wooten, B. A. Racette, J. S. Perlmutter, R. Watts, M. Guttman, K. B. Baker, S. Goldwurm, G. Pezzoli, C. Singer, M. H. Saint-Hilaire, A. E. Hendricks, S. Williamson, M. W. Nagle, J. B. Wilk, T. Massood, J. M. Laramie, A. L. DeStefano, I. Litvan, G. Nicholson, A. Corbett, S. Isaacson, D. J. Burn, P. F. Chinnery, P. P. Pramstaller, S. Sherman, J. Al-hinti, E. Drasby, M. Nance, A. T. Moller, K. Ostergaard, R. Roxburgh, B. Snow, J. T. Slevin, F. Cambi, J. F. Gusella, and R. H. Myers
Neurology 2008; 71: 28-34.
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- ARTICLES
APOE genotype, ethnicity, and the risk of cerebral hemorrhage
- C. Tzourio, H. Arima, S. Harrap, C. Anderson, O. Godin, M. Woodward, B. Neal, M-G Bousser, J. Chalmers, F. Cambien, and S. MacMahon
Neurology 2008; 70: 1322-1328.
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