Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2Olayinka Raheem, Ralf Krahe, Shodimu-Emmanuel Olufemi et al.|American Journal Of Pathology|2010Cited by 75
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2Anna Vihola, Bjarne Udd, Olayinka Raheem et al.|Acta Neuropathologica|2010Cited by 73
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2Rosanna Cardani, G. Meola, Marzia Giagnacovo et al.|Journal of Neurology|2012Cited by 50
Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophiesLinda L. Bachinski, Ralf Krahe, Keith Baggerly et al.|Neuromuscular Disorders|2013Cited by 36
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibersOlayinka Raheem, Bjarne Udd, Sanna Huovinen et al.|Acta Neuropathologica|2010Cited by 31