Meaghan H. Brewer, Ph.D. - Publications

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

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Drew AP, Cutrupi AN, Brewer MH, Nicholson GA, Kennerson ML. A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2. Human Genetics. PMID 27487800 DOI: 10.1007/s00439-016-1720-4  0.356
2016 Brewer MH, Chaudhry R, Qi J, Kidambi A, Drew AP, Menezes MP, Ryan MM, Farrar MA, Mowat D, Subramanian GM, Young HK, Zuchner S, Reddel SW, Nicholson GA, Kennerson ML. Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3. Plos Genetics. 12: e1006177. PMID 27438001 DOI: 10.1371/journal.pgen.1006177  0.335
2015 Drew AP, Zhu D, Kidambi A, Ly C, Tey S, Brewer MH, Ahmad-Annuar A, Nicholson GA, Kennerson ML. Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing. Molecular Genetics & Genomic Medicine. 3: 143-54. PMID 25802885 DOI: 10.1002/mgg3.126  0.402
2013 Chaudhry R, Kidambi A, Brewer MH, Antonellis A, Mathews K, Nicholson G, Kennerson M. Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutation. Muscle & Nerve. 47: 922-4. PMID 23553728 DOI: 10.1002/Mus.23743  0.355
2009 Nicholson G, Kennerson M, Brewer M, Garbern J, Shy M. Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromes. Advances in Experimental Medicine and Biology. 652: 201-6. PMID 20225027 DOI: 10.1007/978-90-481-2813-6_13  0.331
2008 Brewer M, Changi F, Antonellis A, Fischbeck K, Polly P, Nicholson G, Kennerson M. Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb region. Neurogenetics. 9: 191-5. PMID 18458969 DOI: 10.1007/S10048-008-0126-4  0.316
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