Meaghan H. Brewer, Ph.D.

2013 English Temple University, Philadelphia, PA, United States 
Rhetoric and Composition Language, Language and Literature Education
"Meaghan Brewer"


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Eli Goldblatt grad student 2013 Temple University
 (The conceptions of literacy of new graduate instructors teaching composition.)
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Narayanan RK, Brewer MH, Perez-Siles G, et al. (2021) Charcot-Marie-tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6 C. elegans model. Human Molecular Genetics
Kanhangad M, Cornett K, Brewer MH, et al. (2018) Unique clinical and neurophysiologic profile of a cohort of children with CMTX3. Neurology
Drew AP, Cutrupi AN, Brewer MH, et al. (2016) A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2. Human Genetics
Fogarty EA, Brewer MH, Rodriguez-Molina JF, et al. (2016) SOX10 Regulates an Alternative Promoter at the Charcot-Marie-Tooth Disease Locus MTMR2. Human Molecular Genetics
Brewer MH, Chaudhry R, Qi J, et al. (2016) Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3. Plos Genetics. 12: e1006177
Drew AP, Zhu D, Kidambi A, et al. (2015) Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing. Molecular Genetics & Genomic Medicine. 3: 143-54
Brewer MH, Ma KH, Beecham GW, et al. (2014) Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2. Human Molecular Genetics. 23: 5171-87
Chaudhry R, Kidambi A, Brewer MH, et al. (2013) Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutation. Muscle & Nerve. 47: 922-4
Jones EA, Brewer MH, Srinivasan R, et al. (2012) Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22. Human Molecular Genetics. 21: 1581-91
Brewer MH, Chaudhry R, McDowall K, et al. (2010) X-linked CMT: genes and gene loci in an Australian cohort. Neurogenetics. 11: 267-9
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