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Association studies in genetics
Citations 131-140 of 148 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy
- P. Y.W. Man, D. T. Brown, M. S. Wehnert, M. Zeviani, F. Carrara, D. M. Turnbull, and P. F. Chinnery
Neurology 2002; 58: 1861-1862.
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- BRIEF COMMUNICATIONS
Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD?
- E. K. Green, J. M. Harris, H. Lemmon, J. C. Lambert, M. C. Chartier–Harlin, D. St. Clair, D. M.A. Mann, T. Iwatsubo, and C. L. Lendon
Neurology 2002; 58: 1566-1568.
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- ARTICLES
MAOB intron 13 and COMT codon 158 polymorphisms, cigarette smoking, and the risk of PD
- M. A. Hernán, H. Checkoway, R. O’Brien, P. Costa–Mallen, I. De Vivo, G. A. Colditz, D. J. Hunter, K. T. Kelsey, and A. Ascherio
Neurology 2002; 58: 1381-1387.
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- ARTICLES
Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson’s disease
- P.-Y. Xu, R. Liang, J. Jankovic, C. Hunter, Y.-X. Zeng, T. Ashizawa, D. Lai, and W.-D. Le
Neurology 2002; 58: 881-884.
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- BRIEF COMMUNICATIONS
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer disease
- S. Zareparsi, D. M. James, J. A. Kaye, T. D. Bird, G. D. Schellenberg, and H. Payami
Neurology 2002; 58: 973-975.
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Association and linkage of juvenile MS with HLA-DR2(15) in Russians
- A. N. Boiko, E. I. Gusev, M. A. Sudomoina, A. D. Alekseenkov, O. G. Kulakova, O. V. Bikova, O. I. Maslova, M. R. Guseva, S. Y. Boiko, M. E. Guseva, and O. O. Favorova
Neurology 2002; 58: 658-660.
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- CLINICAL/SCIENTIFIC NOTES
A polymorphism in the cystatin C promoter region is not associated with an increased risk of AD
- R. C. Dodel, Y. Du, C. Depboylu, A. Kurz, B. Eastwood, M. Farlow, W. H. Oertel, U. Müller, and M. Riemenschneider
Neurology 2002; 58: 664.
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A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm
- A. Misbahuddin, M.R. Placzek, K.R. Chaudhuri, N.W. Wood, K.P. Bhatia, and T.T. Warner
Neurology 2002; 58: 124-126.
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- BRIEF COMMUNICATIONS
Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy
- Marcel Hungs, Ling Lin, Michele Okun, and Emmanuel Mignot
Neurology 2001; 57: 1893-1895.
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Polymorphisms in hypocretin/orexin pathway genes and narcolepsy
- B. R. Ólafsdóttir, D. B. Rye, T. E. Scammell, J. K. Matheson, K. Stefánsson, and J. R. Gulcher
Neurology 2001; 57: 1896-1899.
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