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Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis.
Barcellos LF, Ramsay PP, Caillier SJ, Sawcer S, Haines J, Schmidt S, Pericak-Vance M, Compston DA, Gabatto P, Hauser SL, Oksenberg JR. Barcellos LF, et al. Among authors: oksenberg jr. Genes Immun. 2008 Sep;9(6):493-500. doi: 10.1038/gene.2008.41. Epub 2008 Jun 26. Genes Immun. 2008. PMID: 18580885 Free PMC article.
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR, et al. Haines JL, et al. Among authors: oksenberg jr. Nat Genet. 1996 Aug;13(4):469-71. doi: 10.1038/ng0896-469. Nat Genet. 1996. PMID: 8696344
Genetics of demyelinating diseases.
Oksenberg JR, Seboun E, Hauser SL. Oksenberg JR, et al. Brain Pathol. 1996 Jul;6(3):289-302. doi: 10.1111/j.1750-3639.1996.tb00856.x. Brain Pathol. 1996. PMID: 8864285 Review.
Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Seboun E, Oksenberg JR, Rombos A, Usuku K, Goodkin DE, Lincoln RR, Wong M, Pham-Dinh D, Boesplug-Tanguy O, Carsique R, Fitoussi R, Gartioux C, Reyes C, Ribierre F, Faure S, Fizames C, Gyapay G, Weissenbach J, Dautigny A, Rimmler JB, Garcia ME, Pericak-Vance MA, Haines JL, Hauser SL. Seboun E, et al. Among authors: oksenberg jr. Neurogenetics. 1999 Sep;2(3):155-62. doi: 10.1007/s100480050076. Neurogenetics. 1999. PMID: 10541588
317 results