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Publications

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

Posted on January 15, 2019

MitjaMitrovič, […], ChrisCotsapas. Cell, Volume 175, Issue 6, 29 November 2018, Pages 1679-1687.e7 Read More

Posted in: Axon Injury & Repair, Publications Faculty:

Impact of Handedness on Disability After Unilateral Upper-Extremity Peripheral Nerve Disorder

Posted on January 15, 2019

Benjamin A. Philip, Vicki Kaskutas, Susan E. Mackinnon. Hand 2018 Read More

Posted in: Axon Injury & Repair, Publications Faculty:

Sex-specific gene and pathway modeling of inherited glioma risk

Posted on January 15, 2019

Quinn T Ostrom Warren Coleman William Huang Joshua B Rubin, […], Jill S Barnholtz-Sloan. Neuro-oncology, Volume 21, Issue 1, 1 January 2019, Pages 71-82 Read More

Posted in: Clocks & Sleep, Neurogenetics & Transcriptomics, Publications Faculty:

Seizures as an early symptom of autosomal dominant Alzheimer’s disease

Posted on January 15, 2019

Jonathan Vöglein, Soheyl Noachtar, Eric McDade, Kimberly A. Quaid, Stephen Salloway, Bernardino Ghetti, James Noble, Sarah Berman, Jasmeer Chhatwal, Hiroshi Mori, Nick Fox, Ricardo Allegri, Colin L. Masters, Virginia Buckles, John M. Ringman, Martin Rossor, Peter R. Schofieldo, Reisa Sperling, Mathias Jucker, Christoph Laske, Katrina Paumier, John C. Morris, Randall J. Bateman, Johannes Levina, Adrian Daneka, for the Dominantly Inherited Alzheimer Network. Neurobiology of Aging, Volume 76, April 2019, Pages 18-23 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty: ,

Epigenetic regulator UHRF1 inactivates REST and growth suppressor gene expression via DNA methylation to promote axon regeneration

Posted on January 10, 2019

Young Mi Oh, Marcus Mahar, Eric E. Ewan, Kathleen M. Leahy, Guoyan Zhao, and Valeria Cavalli. Proceedings of the National Academy of Sciences of the United States of America, Volume 115, Issue 52, 26 December 2018, Pages E12417-E12426 Read More

Posted in: Axon Injury & Repair, Publications Faculty: