Meghan C. Drummond

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh et al. · The American Journal of Human Genetics · 2013 · 238 citations · Full text

Mitochondrial Function, Genetic Disorder, Medicine +7

Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome

Kevin Isgrig, Jack W. Shteamer, Inna A. Belyantseva et al. · Molecular Therapy · 2017 · 167 citations · Full text

Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice

Wade W. Chien, Kevin Isgrig, Soumen Roy et al. · Molecular Therapy · 2015 · 99 citations · Full text

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Atteeq U. Rehman, Regie Lyn P. Santos‐Cortez, Robert J. Morell et al. · The American Journal of Human Genetics · 2014 · 86 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Live-cell imaging of actin dynamics reveals mechanisms of stereocilia length regulation in the inner ear

Meghan C. Drummond, Melanie Barzik, Jonathan E. Bird et al. · Nature Communications · 2015 · 82 citations · Full text