| Year |
Citation |
Score |
| 2022 |
Praveen K, Dobbyn L, Gurski L, Ayer AH, Staples J, Mishra S, Bai Y, Kaufman A, Moscati A, Benner C, Chen E, Chen S, Popov A, Smith J, Melander O, ... ... Drummond MC, et al. Population-scale analysis of common and rare genetic variation associated with hearing loss in adults. Communications Biology. 5: 540. PMID 35661827 DOI: 10.1038/s42003-022-03408-7 |
0.358 |
|
| 2017 |
Isgrig K, Shteamer JW, Belyantseva IA, Drummond MC, Fitzgerald TS, Vijayakumar S, Jones SM, Griffith AJ, Friedman TB, Cunningham LL, Chien WW. Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 28254438 DOI: 10.1016/J.Ymthe.2017.01.007 |
0.479 |
|
| 2016 |
Krey JF, Drummond M, Foster S, Porsov E, Vijayakumar S, Choi D, Friderici K, Jones SM, Nuttall AL, Barr-Gillespie PG. Annexin A5 is the Most Abundant Membrane-Associated Protein in Stereocilia but is Dispensable for Hair-Bundle Development and Function. Scientific Reports. 6: 27221. PMID 27251877 DOI: 10.1038/Srep27221 |
0.593 |
|
| 2015 |
Chien WW, Isgrig K, Roy S, Belyantseva IA, Drummond MC, May LA, Fitzgerald TS, Friedman TB, Cunningham LL. Gene therapy restores hair cell stereocilia morphology in inner ears of deaf whirler mice. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 26307667 DOI: 10.1038/Mt.2015.150 |
0.436 |
|
| 2015 |
Drummond MC, Barzik M, Bird JE, Zhang DS, Lechene CP, Corey DP, Cunningham LL, Friedman TB. Live-cell imaging of actin dynamics reveals mechanisms of stereocilia length regulation in the inner ear. Nature Communications. 6: 6873. PMID 25898120 DOI: 10.1038/Ncomms7873 |
0.32 |
|
| 2014 |
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, et al. Challenges and solutions for gene identification in the presence of familial locus heterogeneity. European Journal of Human Genetics : Ejhg. PMID 25491636 DOI: 10.1038/Ejhg.2014.266 |
0.479 |
|
| 2014 |
Rehman AU, Santos-Cortez RL, Morell RJ, Drummond MC, Ito T, Lee K, Khan AA, Basra MA, Wasif N, Ayub M, Ali RA, Raza SI, Nickerson DA, Shendure J, et al. Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. American Journal of Human Genetics. 94: 144-52. PMID 24387994 DOI: 10.1016/J.Ajhg.2013.12.004 |
0.468 |
|
| 2014 |
Lovell KL, Zhu M, Drummond MC, Switzer RC, Friderici KH. Distribution and Severity of Neuropathology in β-Mannosidase-Deficient Mice is Strain Dependent. Jimd Reports. 13: 73-81. PMID 24142277 DOI: 10.1007/8904_2013_258 |
0.549 |
|
| 2013 |
Drummond MC, Friderici KH. A novel actin mRNA splice variant regulates ACTG1 expression. Plos Genetics. 9: e1003743. PMID 24098136 DOI: 10.1371/Journal.Pgen.1003743 |
0.567 |
|
| 2013 |
Jenkinson EM, Rehman AU, Walsh T, Clayton-Smith J, Lee K, Morell RJ, Drummond MC, Khan SN, Naeem MA, Rauf B, Billington N, Schultz JM, Urquhart JE, Lee MK, Berry A, et al. Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease. American Journal of Human Genetics. 92: 605-13. PMID 23541340 DOI: 10.1016/J.Ajhg.2013.02.013 |
0.396 |
|
| 2012 |
Drummond MC, Belyantseva IA, Friderici KH, Friedman TB. Actin in hair cells and hearing loss. Hearing Research. 288: 89-99. PMID 22200607 DOI: 10.1016/J.Heares.2011.12.003 |
0.643 |
|
| 2006 |
Fyfe JC, Menotti-Raymond M, David VA, Brichta L, Schäffer AA, Agarwala R, Murphy WJ, Wedemeyer WJ, Gregory BL, Buzzell BG, Drummond MC, Wirth B, O'Brien SJ. An approximately 140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival. Genome Research. 16: 1084-90. PMID 16899656 DOI: 10.1101/Gr.5268806 |
0.393 |
|
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