Incidental MRI anomalies suggestive of multiple sclerosis : The radiologically isolated syndrome von OKUDA, D. T, MOWRY, E. M, BEHESHTIAN, A, WAUBANT, E, BARANZINI, S. E, GOODIN, D. S, HAUSER, S. L, PELLETIER, D

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Blood miRNA expression pattern is a possible risk marker for natalizumab-associated progressive multifocal leukoencephalopathy in multiple sclerosis patients von Muñoz-Culla, M, Irizar, H, Castillo-Triviño, T, Sáenz-Cuesta, M, Sepúlveda, L, Lopetegi, I, de Munain, A López, Olascoaga, J, Baranzini, SE, Otaegui, D

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Genetic associations with brain cortical thickness in multiple sclerosis von Matsushita, T., Madireddy, L., Sprenger, T., Khankhanian, P., Magon, S., Naegelin, Y., Caverzasi, E., Lindberg, R. L. P., Kappos, L., Hauser, S. L., Oksenberg, J. R., Henry, R., Pelletier, D., Baranzini, S. E.

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Transcriptional expression patterns triggered by chemically distinct neuroprotective molecules von Pappas, D.J, Gabatto, P.A, Oksenberg, D, Khankhanian, P, Baranzini, S.E, Gan, L, Oksenberg, J.R

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Longitudinal system-based analysis of transcriptional responses to type I interferons von Pappas, D. J, Coppola, G, Gabatto, P. A, Gao, F, Geschwind, D. H, Oksenberg, J. R, Baranzini, S. E

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Pathway and network-based analysis of genome-wide association studies in multiple sclerosis von Baranzini, Sergio E., Galwey, Nicholas W., Wang, Joanne, Khankhanian, Pouya, Lindberg, Raija, Pelletier, Daniel, Wu, Wen, Uitdehaag, Bernard M.J., Kappos, Ludwig, Polman, Chris H., Matthews, Paul M., Hauser, Stephen L., Gibson, Rachel A., Oksenberg, Jorge R., Barnes, Michael R.

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Transcriptional Analysis of Multiple Sclerosis Brain Lesions Reveals a Complex Pattern of Cytokine Expression von Baranzini, Sergio E, Elfstrom, Carita, Chang, Sheng-Yung, Butunoi, Catalin, Murray, Ronald, Higuchi, Russell, Oksenberg, Jorge R

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Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis von Sriram, U, Barcellos, L F, Villoslada, P, Rio, J, Baranzini, S E, Caillier, S, Stillman, A, Hauser, S L, Montalban, X, Oksenberg, J R

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Multiple sclerosis: Genomic rewards von Oksenberg, Jorge R, Baranzini, Sergio E, Barcellos, Lisa F, Hauser, Stephen L

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Osteopontin polymorphisms and disease course in multiple sclerosis von Caillier, S, Barcellos, L F, Baranzini, S E, Swerdlin, A, Lincoln, R R, Steinman, L, Martin, E, Haines, J L, Pericak-Vance, M, Hauser, S L, Oksenberg, J R

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The autoimmune risk gene ZMIZ1 is a vitamin D responsive marker of a molecular phenotype of multiple sclerosis von Fewings, N.L, Gatt, P.N, McKay, F.C, Parnell, G.P, Schibeci, S.D, Edwards, J, Basuki, M.A, Goldinger, A, Fabis-Pedrini, M.J, Kermode, A.G, Manrique, C.P, McCauley, J.L, Nickles, D, Baranzini, S.E, Burke, T, Vucic, S, Stewart, G.J, Booth, D.R

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Genotype-Phenotype Correlations in Multiple Sclerosis: "HLA" Genes Influence Disease Severity Inferred by [superscript 1]HMR Spectroscopy and MRI Measures von Okuda, D. T, Srinivasan, R, Oksenberg, J. R, Goodin, D. S, Baranzini, S. E, Beheshtian, A, Waubant, E, Zamvil, S. S, Leppert, D, Qualley, P, Lincoln, R, Gomez, R, Caillier, S, George, M, Wang, J, Nelson, S. J, Cree, B. A. C, Hauser, S. L, Pelletier, D

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Genotype–Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measures von Okuda, D. T., Srinivasan, R., Oksenberg, J. R., Goodin, D. S., Baranzini, S. E., Beheshtian, A., Waubant, E., Zamvil, S. S., Leppert, D., Qualley, P., Lincoln, R., Gomez, R., Caillier, S., George, M., Wang, J., Nelson, S. J., Cree, B. A. C., Hauser, S. L., Pelletier, D.

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The Influence of the Proinflammatory Cytokine, Osteopontin, on Autoimmune Demyelinating Disease von Chabas, Dorothée, Baranzini, Sergio E., Mitchell, Dennis, Claude C. A. Bernard, Rittling, Susan R., Denhardt, David T., Sobel, Raymond A., Lock, Christopher, Karpuj, Marcela, Pedotti, Rosetta, Heller, Renu, Oksenberg, Jorge R., Steinman, Lawrence

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Analysis of antibody gene rearrangement, usage, and specificity in chronic focal encephalitis von BARANZINI, S. E, LAXER, K, SAKETKHOO, R, ELKINS, M. K, PARENT, J. M, MANTEGAZZA, R, OKSENBERG, J. R

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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1 von Slavotinek, Anne M, Baranzini, Sergio E, Schanze, Denny, Labelle-Dumais, Cassandre, Short, Kieran M, Chao, Ryan, Yahyavi, Mani, Bijlsma, Emilia K, Chu, Catherine, Musone, Stacey, Wheatley, Ashleigh, Kwok, Pui-Yan, Marles, Sandra, Fryns, Jean-Pierre, Maga, A Murat, Hassan, Mohamed G, Gould, Douglas B, Madireddy, Lohith, Li, Chumei, Cox, Timothy C, Smyth, Ian, Chudley, Albert E, Zenker, Martin

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B Cell Repertoire Diversity and Clonal Expansion in Multiple Sclerosis Brain Lesions von Baranzini, Sergio E, Jeong, Matthew C, Butunoi, Catalin, Murray, Ronald S, Bernard, Claude C. A, Oksenberg, Jorge R

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Data characterizing the ZMIZ1 molecular phenotype of multiple sclerosis von Fewings, N., Gatt, P.N., McKay, F.C., Parnell, G.P., Schibeci, S.D., Edwards, J., Basuki, M.A., Goldinger, A., Fabis-Pedrini, M.J., Kermode, A.G., Manrique, C.P., McCauley, J.L., Nickles, D., Baranzini, S.E., Burke, T., Vucic, S., Stewart, G.J., Booth, D.R.

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The genetics of autoimmune diseases: a networked perspective von Baranzini, Sergio E

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Four new polymorphisms in the human dystrophin gene from an Argentinian population von Baranzini, Sergio Enrique, Lenk, Uwe, Szijan, Irena, Speer, Astrid

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