Publications

Axin2 as regulatory and therapeutic target in newborn brain injury and remyelination.

Fancy SP, Harrington EP, Yuen TJ, Silbereis JC, Zhao C, Baranzini SE, Bruce CC, Otero JJ, Huang EJ, Nusse R, Franklin RJ, Rowitch DH

Nature neuroscience, 2011

Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.

Slavotinek AM, Baranzini SE, Schanze D, Labelle-Dumais C, Short KM, Chao R, Yahyavi M, Bijlsma EK, Chu C, Musone S, Wheatley A, Kwok PY, Marles S, Fryns JP, Maga AM, Hassan MG, Gould DB, Madireddy L, Li C, Cox TC, Smyth I, Chudley AE, Zenker M

Journal of medical genetics, 2011

Functional energetics of CD4+-cellular immunity in monoclonal antibody-associated progressive multifocal leukoencephalopathy in autoimmune disorders.

Haghikia A, Perrech M, Pula B, Ruhrmann S, Potthoff A, Brockmeyer NH, Goelz S, Wiendl H, Lindå H, Ziemssen T, Baranzini SE, Käll TB, Bengel D, Olsson T, Gold R, Chan A

PloS one, 2011

Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.

Wang JH, Pappas D, De Jager PL, Pelletier D, de Bakker PI, Kappos L, Polman CH, Chibnik LB, Hafler DA, Matthews PM, Hauser SL, Baranzini SE, Oksenberg JR

Genome medicine, 2011

Revealing the genetic basis of multiple sclerosis: are we there yet?

Baranzini SE

Current opinion in genetics & development, 2011

Dynamic, multi-level network models of clinical trials.

Sorani MD, Manley GT, Claude Hemphill J, Baranzini SE

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2011

Myelin regeneration: a recapitulation of development?

Fancy SP, Chan JR, Baranzini SE, Franklin RJ, Rowitch DH

Annual review of neuroscience, 2011

Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset.

Khankhanian P, Gourraud PA, Caillier SJ, Santaniello A, Hauser SL, Baranzini SE, Oksenberg JR

BMC genomics, 2010

Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.

Baranzini SE, Srinivasan R, Khankhanian P, Okuda DT, Nelson SJ, Matthews PM, Hauser SL, Oksenberg JR, Pelletier D

Brain : a journal of neurology, 2010

Multiple sclerosis genetics--is the glass half full, or half empty?

Oksenberg JR, Baranzini SE

Nature reviews. Neurology, 2010

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