Browsing by Author de Andrade, M.

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Showing results 1 to 6 of 6
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Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson diseaseMaraganore, D. M.; de Andrade, M.; Elbaz, A.; Farrer, M. J.; Ioannidis, J. P.; Kruger, R.; Rocca, W. A.; Schneider, N. K.; Lesnick, T. G.; Lincoln, S. J.; Hulihan, M. M.; Aasly, J. O.; Ashizawa, T.; Chartier-Harlin, M. C.; Checkoway, H.; Ferrarese, C.; Hadjigeorgiou, G.; Hattori, N.; Kawakami, H.; Lambert, J. C.; Lynch, T.; Mellick, G. D.; Papapetropoulos, S.; Parsian, A.; Quattrone, A.; Riess, O.; Tan, E. K.; Van Broeckhoven, C.24-Nov-2015-
Genetic polymorphisms in glutathione S-transferase mu and theta, N-acetyltransferase, and CYP1A1 and risk of gliomasTrizna, Z.; de Andrade, M.; Kyritsis, A. P.; Briggs, K.; Levin, V. A.; Bruner, J. M.; Wei, Q.; Bondy, M. L.24-Nov-2015-
Increased chromosomal instability in peripheral lymphocytes and risk of human gliomasEl-Zein, R.; Bondy, M. L.; Wang, L. E.; de Andrade, M.; Sigurdson, A. J.; Bruner, J. M.; Kyritsis, A. P.; Levin, V. A.; Wei, Q.24-Nov-2015-
Mutagen sensitivity and risk of gliomas: a case-control analysisBondy, M. L.; Kyritsis, A. P.; Gu, J.; de Andrade, M.; Cunningham, J.; Levin, V. A.; Bruner, J. M.; Wei, Q.24-Nov-2015-
Risk assessment for developing gliomas: a comparison of two cytogenetic approachesEl-Zein, R.; Bondy, M. L.; Wang, L. E.; de Andrade, M.; Sigurdson, A. J.; Bruner, J. M.; Kyritsis, A. P.; Levin, V. A.; Wei, Q.24-Nov-2015-
UCHL1 is a Parkinson's disease susceptibility geneMaraganore, D. M.; Lesnick, T. G.; Elbaz, A.; Chartier-Harlin, M. C.; Gasser, T.; Kruger, R.; Hattori, N.; Mellick, G. D.; Quattrone, A.; Satoh, J.; Toda, T.; Wang, J.; Ioannidis, J. P.; de Andrade, M.; Rocca, W. A.24-Nov-2015-