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• Specific hypomethylation programs underpin B cell activation in early multiple sclerosis.

  Authors:Qin Ma, Stacy J. Caillier, Shaun Muzic, Michael R. Wilson, Roland G. Henry, Bruce A. C. Cree, et al.From:Proceedings of the National Academy of Sciences of the United States (Vol. 118, Issue 51) Peer-Reviewed

  Dec. 21, 20217,180 words Report 1450L

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• Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

  Authors:Mitja Mitrovic, Nikolaos A. Patsopoulos, Ashley H. Beecham, Theresa Dankowski, An Goris, Benedicte Dubois, et al.From:Cell (Vol. 175, Issue 6) Peer-Reviewed

  Nov. 29, 2018537 words Article

   Abstract Only

• Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event

  Authors:Jean-Christophe Corvol, Daniel Pelletier, Roland G. Henry, Stacy J. Caillier, Joanne Wang, Derek Pappas, et al.From:Proceedings of the National Academy of Sciences of the United States (Vol. 105, Issue 33) Peer-Reviewed

  Aug. 19, 2008203 words Author abstract, Rep...

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• MIF and D-DT are potential disease severity modifiers in male MS subjects

  Authors:Gil Benedek, Roberto Meza-Romero, Kelley Jordan, Ying Zhang, Ha Nguyen, Gail Kent, et al.From:Proceedings of the National Academy of Sciences of the United States (Vol. 114, Issue 40) Peer-Reviewed

  Oct. 3, 20178,730 words Article 1490L

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• Ataxin-1 regulates B cell function and the severity of autoimmune experimental encephalomyelitis

  Authors:Alessandro Didonna, Ester Canto Puig, Qin Ma, Atsuko Matsunaga, Brenda Ho, Stacy J. Caillier, et al.From:Proceedings of the National Academy of Sciences of the United States (Vol. 117, Issue 38) Peer-Reviewed

  Sept. 22, 20207,204 words Report 1490L

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• Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

  Authors:Sergio E. Baranzini, Joann Mudge, Jennifer C. van Velkinburgh, Pouya Khankhanian, Irina Khrebtukova, Neil A. Miller, et al.From:Nature (Vol. 464, Issue 7293) Peer-Reviewed

  Apr. 29, 20107,033 words Report 1550LMonozygotic or 'identical' twins have been widely studied to dissect the relative contributions of genetics and environment in human diseases. In multiple sclerosis (MS), an autoimmune demyelinating disease and common...

• The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

  Authors:Ann B. Begovich, Stacy J. Caillier, Heather C. Alexander, Joanne M. Penko, Stephen L. Hauser, Lisa F. Barcellos, et al.From:American Journal of Human Genetics (Vol. 76, Issue 1) Peer-Reviewed

  Jan. 2005 Letter to the editor

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