Publications

Recent Publications

Pappas D.J., G. Coppola, P.A. Gabatto, F. Goa, D.H. Geschwind, J.R. Oksenberg, S.E. Baranzini. Longitudinal system-based analysis of transcriptional responses to type I interferons. Physiol Genomics. 2009.
PMID: 19531577

De Jager P.L., P.I.W. de Bakker, J. Wang, L. Ottoboni, S. Xia, N.T. Aggarwal, L. Piccio, S. Raychudhuri, D. Tran, C. Aubin, R. Briskin, S. Romano, International MS Genetics Consortium, S.E. Baranzini, J. McCauley, M. Pericak-Vance, J. Haines, R.A. Gibson, Y. Naeglin, P.M. Matthew, L. Kappos, C. Polman, W.L. McArdle, D.P. Strachan, D. Evans, A.H. Cross, M.J. Daly, A. Compston, S.J. Sawcer, H.L. Weiner, S.L. Hauser, D.A. Hafler, J.R. Oksenberg. Meta-analysis of genome scans and replication identify CD6, ICSBP1, and TNFRSF1A as novel multiple sclerosis susceptibility loci. Nat. Genet. 2009.
PMID: 19525953

McElroy J.P., M.R. Nelson, S.J. Caillier, J.R. Oksenberg. Copy number variation in African Americans. BMC Genetics. 2009.
PMID: 19317893

Baranzini S.E., N.W. Galwey, J. Wang, P. Khankhanian, R. Lindberg, D. Pelletier, W. Wu, B.M. Uitdehaag, GeneMSA Consortium, L. Kappos, C.H. Polman, P.M. Matthews, S.L. Hauser SL, R.A. Gibson, J.R. Oksenberg, M.R. Barnes. Pathway and network-based analysis of genome-wide association studies in multiple sclerosis. Hum. Molec. Genet. 2009.
PMID: 19286671

Cree B.A.C., D.E. Reich, O. Khan, P.L. De Jagger, I. Nakashima, T. Takahashi, A. Bar-Or, C. Tong, S.L. Hauser, J.R. Oksenberg. Modification of multiple sclerosis phenotypes by African ancestry at HLA. Arch. Neurol. 2009.
PMID: 19204159

Baranzini S.E., J. Wang, R.A. Gibson, N. Galwey, Y. Naegelin, F. Barkhof, E.W. Radue, R.L. Lindberg, B. Uitdehaag, M.R. Johnson, A. Angelakopoulou, L. Hall, J.C. Richardson, R.K. Prinjha, A. Gass, J.J. Geurts, J. Kragt, M. Sombekke, H. Vrenken, P. Qualley, R.R. Lincoln, R. Gomez, S.J. Caillier, M.F. George, H. Mousavi, R. Guerrero, D.T. Okuda, B.A. Cree, A. Green, E. Waubant, D.S. Goodin, D. Pelletier, P.M. Matthews, S.L. Hauser, L. Kappos, C.H. Polman, J.R. Oksenberg. Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Hum. Molec. Genet. 2009.
PMID: 19010793

Okuda D.T., R. Srinivasan, J.R. Oksenberg, D.S. Goodin, S.E. Baranzini, E. Waubant, SS. Zamvil, P. Qualley, R. Lincoln, R. Gomez, S. Caillier, M. George, J. Wang, S.J. Nelson, B.A.C. Cree, S.L. Hauser, D. Pelletier. Genotype-Phenotype correlation in multiple sclerosis: HLA genes influence axonal integrity inferred by 1HMR spectroscopy and MRI measures. Brain. 2009.
PMID: 19022862

Hermiston M.L., J. Zikherman, A.L. Tan, V.C. Lam, N.M. Cresalia, N. Oksenberg, N. Goren, D. Brassat, J.R, Oksenberg, A. Weiss. Differential impact of the CD45 juxtamembrane wedge on central and peripheral T cell receptor responses. Proc. Natl. Acad. Sci. USA. 2009.
PMID: 19129486

International Multiple Sclerosis Genetics Consortium. The expanding genetic overlap between multiple sclerosis and type I diabetes. Genes and Immunity. 2009.
PMID: 18987646