Meaghan H. Brewer, Ph.D. - Publications

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

13/15 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
2021 Narayanan RK, Brewer MH, Perez-Siles G, Ellis M, Ly C, Burgess A, Neumann B, Nicholson GA, Vucic S, Kennerson ML. 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. PMID 34387338 DOI: 10.1093/hmg/ddab228  1
2018 Kanhangad M, Cornett K, Brewer MH, Nicholson GA, Ryan MM, Smith RL, Subramanian GM, Young HK, Züchner S, Kennerson ML, Burns J, Menezes MP. Unique clinical and neurophysiologic profile of a cohort of children with CMTX3. Neurology. PMID 29626178 DOI: 10.1212/Wnl.0000000000005479  1
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  1
2016 Fogarty EA, Brewer MH, Rodriguez-Molina JF, Law WD, Ma KH, Steinberg NM, Svaren J, Antonellis A. SOX10 Regulates an Alternative Promoter at the Charcot-Marie-Tooth Disease Locus MTMR2. Human Molecular Genetics. PMID 27466180 DOI: 10.1093/Hmg/Ddw233  1
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  1
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  1
2014 Brewer MH, Ma KH, Beecham GW, Gopinath C, Baas F, Choi BO, Reilly MM, Shy ME, Züchner S, Svaren J, Antonellis A. 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. PMID 24833716 DOI: 10.1093/Hmg/Ddu240  1
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  1
2012 Jones EA, Brewer MH, Srinivasan R, Krueger C, Sun G, Charney KN, Keles S, Antonellis A, Svaren J. Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22. Human Molecular Genetics. 21: 1581-91. PMID 22180461 DOI: 10.1093/Hmg/Ddr595  1
2010 Brewer MH, Chaudhry R, McDowall K, Chu S, Kowalski B, Polly P, Nicholson G, Kennerson M. X-linked CMT: genes and gene loci in an Australian cohort. Neurogenetics. 11: 267-9. PMID 20204443 DOI: 10.1007/s10048-010-0238-5  1
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  1
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  1
2007 Kennerson ML, Warburton T, Nelis E, Brewer M, Polly P, De Jonghe P, Timmerman V, Nicholson GA. Mutation scanning the GJB1 gene with high-resolution melting analysis: implications for mutation scanning of genes for Charcot-Marie-Tooth disease. Clinical Chemistry. 53: 349-52. PMID 17200131 DOI: 10.1373/Clinchem.2006.080010  1
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2018 Cutrupi AN, Brewer MH, Nicholson GA, Kennerson ML. Structural variations causing inherited peripheral neuropathies: A paradigm for understanding genomic organization, chromatin interactions, and gene dysregulation. Molecular Genetics & Genomic Medicine. 6: 422-433. PMID 29573232 DOI: 10.1002/mgg3.390  0.01
2016 Auer-Grumbach M, Bennett DLH, Andersen P, Harms MB, Reilly MM, Weishaupt J, Strom TM, Walther T, Scherer SS, Zuchner S, Martini R, Senderek J. Rare Coding Variants In The Mme Gene, Encoding The Metalloprotease Neprilysin, Are Linked To Late-Onset Axonal Neuropathies Journal of the Peripheral Nervous System. 21: 235-235. DOI: 10.1111/Jns.12181  0.01
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