Megan H. Brewer - Concepedia

Author

Megan H. Brewer

Anzac Research Institute

Also Known As

Megan Brewer, Megan H Brewer, Megan H. Brewer, Megan Hwa Brewer

Publications

313

Citations

H-Index

Concepts

All Affiliations

Anzac Research Institute Concord Repatriation General Hospital The University of Sydney University of Michigan University of Iowa

About

Megan H. Brewer is an author at Anzac Research Institute specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	57
2	Natural Sciences	1	1	13
3	Social Sciences	1	1	10
4	Cell Biology	1	1	10
5	Molecular Biology	1	1	13

Megan H. Brewer

Publications

257

Citations

H-Index

Page 1

	Year	Citations
Improved inherited peripheral neuropathy genetic diagnosis by whole‐exome sequencing Alexander P. Drew, Danqing Zhu, Aditi Kidambi, Molecular Genetics & Genomic Medicine	2015	68
Mutation Scanning the GJB1 Gene with High-Resolution Melting Analysis: Implications for Mutation Scanning of Genes for Charcot-Marie-Tooth Disease Marina Kennerson, Trent Warburton, Eva Nelis, Clinical Chemistry	2007	57
Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22 Erin A. Jones, Megan H. Brewer, Rajini Srinivasan, Human Molecular Genetics	2011	39
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3 Megan H. Brewer, Rabia Chaudhry, Jessica Qi, PLoS Genetics Kb InsertionNeurogenomicsGeneticsGenetic EpidemiologyPathology	2016	34
Haplotype-specific modulation of a SOX10/CREB response element at the Charcot–Marie–Tooth disease type 4C locus SH3TC2 Megan H. Brewer, Gary W. Beecham, Chetna Gopinath, Human Molecular Genetics	2014	23
Re‐analysis of an original <scp><i>CMTX3</i></scp> family using exome sequencing identifies a known <scp><i>BSCL2</i></scp> mutation Rabia Chaudhry, Aditi Kidambi, Megan H. Brewer, Muscle & Nerve	2012	13
A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34–q36.2 Alexander P. Drew, Anthony N. Cutrupi, Megan H. Brewer, Human Genetics CytogeneticsGeneticsMolecular BiologyMolecular GeneticsChromosome 22	2016	13
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<i>C. elegans</i>model Ramesh K. Narayanan, Megan H. Brewer, Gonzalo Pérez‐Siles, Human Molecular Genetics Axonal CmtGeneticsSynaptic TransmissionCharcot–marie–tooth DiseaseSynaptic Signaling	2021	10

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