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Jennifer C. Schymick, D.Phil.

Affiliations: 
University of California Irvine School of Medicine, Irvine, CA, United States 
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Parents

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Andrew Singleton grad student 2005-2009 National Institute of Health
Kevin Talbot grad student 2005-2009 Oxford
Bryan J. Traynor grad student 2005-2009 National Institute of Health

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Publications

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Xi Z, Zinman L, Moreno D, et al. (2013) Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion American Journal of Human Genetics. 92: 981-989
Schymick JC, Traynor BJ. (2012) Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia. Alzheimer's Research & Therapy. 4: 30
Mok K, Traynor BJ, Schymick J, et al. (2012) Chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiology of Aging. 33: 209.e3-8
Renton AE, Majounie E, Waite A, et al. (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron. 72: 257-68
Lai SL, Abramzon Y, Schymick JC, et al. (2011) FUS mutations in sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 32: 550.e1-4
Del Bo R, Corti S, Santoro D, et al. (2011) No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiology of Aging. 32: 1157-8
Johnson JO, Mandrioli J, Benatar MG, et al. (2011) Erratum exome sequencing reveals VCP mutations as a cause of familial ALS Neuron. 69
Johnson JO, Mandrioli J, Benatar M, et al. (2010) Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron. 68: 857-64
Laaksovirta H, Peuralinna T, Schymick JC, et al. (2010) Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. The Lancet. Neurology. 9: 978-85
Chiò A, Calvo A, Moglia C, et al. (2010) Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations. Archives of Neurology. 67: 1002-9
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