Meaghan H. Brewer, Ph.D.

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

Parents

Sign in to add mentor
Eli Goldblatt grad student 2013 Temple University
 (The conceptions of literacy of new graduate instructors teaching composition.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...