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Association studies in genetics
Citations 1-10 of 127 total displayed.
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Most recent content
(6 Jan 2009):
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- ARTICLES
Smoking and family history and risk of aneurysmal subarachnoid hemorrhage
- D. Woo, J. Khoury, M. M. Haverbusch, P. Sekar, M. L. Flaherty, D. O. Kleindorfer, B. M. Kissela, C. J. Moomaw, R. Deka, and J. P. Broderick
Neurology 2009; 72: 69-72.
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Past content
(since Jan 2001):
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- EDITORIALS
Hereditary motor neuropathy and heat shock proteins: A shocking transformation
- Clifton Gooch and Michael Shy
Neurology 2008; 71: 1656-1657.
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- ARTICLES
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
- C. H. Lin, E. K. Tan, M. L. Chen, L. C. Tan, H. Q. Lim, G. S. Chen, and R. M. Wu
Neurology 2008; 71: 1727-1732.
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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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- 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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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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