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Association studies in genetics
Citations 101-110 of 147 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
LGI1 mutations in temporal lobe epilepsies
- S. F. Berkovic, P. Izzillo, J. M. McMahon, L. A. Harkin, A. M. McIntosh, H. A. Phillips, R. S. Briellmann, R. H. Wallace, A. Mazarib, M. Y. Neufeld, A. D. Korczyn, I. E. Scheffer, and J. C. Mulley
Neurology 2004; 62: 1115-1119.
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- CLINICAL/SCIENTIFIC NOTES
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease
- R. Hering, S. Petrovic, E. -M. Mietz, C. Holzmann, D. Berg, P. Bauer, D. Woitalla, T. Müller, K. Berger, R. Krüger, and O. Riess
Neurology 2004; 62: 1231-1232.
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- BRIEF COMMUNICATIONS
TNF-376A marks susceptibility to MS in the Spanish population: A replication study
- A. Martínez, A. Rubio, E. Urcelay, M. Fernández-Arquero, V. de las Heras, R. Arroyo, P. Villoslada, X. Montalbán, and E.G. de la Concha
Neurology 2004; 62: 809-810.
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- BRIEF COMMUNICATIONS
Association of APOE polymorphisms with disease severity in MS is limited to women
- O. H. Kantarci, D. D. Hebrink, S. J. Achenbach, S. J. Pittock, A. Altintas, J. L. Schaefer-Klein, E. J. Atkinson, M. de Andrade, C. T. McMurray, M. Rodriguez, and B. G. Weinshenker
Neurology 2004; 62: 811-814.
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- BRIEF COMMUNICATIONS
Confirmation of the protective effect of iNOS in an independent cohort of Parkinson disease
- S. Hague, T. Peuralinna, J. Eerola, O. Hellström, P. J. Tienari, and A. B. Singleton
Neurology 2004; 62: 635-636.
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- ARTICLES
A haplotype at the PARK3 locus influences onset age for Parkinson’s disease: The GenePD study
- S. Karamohamed, A. L. DeStefano, J. B. Wilk, C. M. Shoemaker, L. I. Golbe, M. H. Mark, A. M. Lazzarini, O. Suchowersky, N. Labelle, M. Guttman, L. J. Currie, G. F. Wooten, M. Stacy, M. Saint-Hilaire, R. G. Feldman, K. M. Sullivan, G. Xu, R. Watts, J. Growdon, M. Lew, C. Waters, P. Vieregge, P. P. Pramstaller, C. Klein, B. A. Racette, J. S. Perlmutter, A. Parsian, C. Singer, E. Montgomery, K. Baker, J. F. Gusella, S. J. Fink, R. H. Myers, and A. Herbert
Neurology 2003; 61: 1557-1561.
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- ARTICLES
 B-Crystallin genotype has impact on the multiple sclerosis phenotype
- T. van Veen, L. van Winsen, J. B.A. Crusius, N. F. Kalkers, F. Barkhof, A. S. Peña, C. H. Polman, and B. M.J. Uitdehaag
Neurology 2003; 61: 1245-1249.
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- ARTICLES
Candidate gene studies in focal dystonia
- D. Sibbing, F. Asmus, I. R. König, S. Tezenas du Montcel, M. Vidailhet, S. Sangla, W. H. Oertel, A. Brice, A. Ziegler, T. Gasser, and O. Bandmann
Neurology 2003; 61: 1097-1101.
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- BRIEF COMMUNICATIONS
Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD
- J. Eerola, D. Hernandez, J. Launes, O. Hellström, S. Hague, C. Gulick, J. Johnson, T. Peuralinna, J. Hardy, P. J. Tienari, and A. B. Singleton
Neurology 2003; 61: 1000-1002.
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- BRIEF COMMUNICATIONS
A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy
- D. Audenaert, L. Claes, B. Ceulemans, A. Löfgren, C. Van Broeckhoven, and P. De Jonghe
Neurology 2003; 61: 854-856.
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