Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2Pankaj B. Agrawal, Alan H. Beggs, Rebecca S. Greenleaf et al.|The American Journal of Human Genetics|2006Cited by 237
Expression profiling and identification of novel genes involved in myogenic differentiationKinga K. Tomczak, Alan H. Beggs, Mei Han et al.|The FASEB Journal|2003Cited by 183
Heterogeneity of nemaline myopathy cases with skeletal muscle α‐actin gene mutationsPankaj B. Agrawal, Alan H. Beggs, Corinne D. Strickland et al.|Annals of Neurology|2004Cited by 145
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscleKarim Hnia, Jocelyn Laporte, Hélène Tronchère et al.|Journal of Clinical Investigation|2010Cited by 140
X-Linked Myotubular and Centronuclear MyopathiesChristopher R. Pierson, Alan H. Beggs, Kinga K. Tomczak et al.|Journal of Neuropathology & Experimental Neurology|2005Cited by 111