| Guidelines for the use and interpretation of assays for monitoring autophagy CM McDermott Autophagy 8 (4), 445, 2012 | 13474* | 2012 |
| Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy J Sarparanta, PH Jonson, C Golzio, S Sandell, H Luque, M Screen, ... Nature Genetics, 2012 | 279 | 2012 |
| Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1 P Hackman, J Sarparanta, S Lehtinen, A Vihola, A Evilä, PH Jonson, ... Annals of Neurology, 2012 | 165 | 2012 |
| Atypical phenotypes in titinopathies explained by second titin mutations A Evilä, A Vihola, J Sarparanta, O Raheem, J Palmio, S Sandell, ... Annals of neurology 75 (2), 230-240, 2014 | 84 | 2014 |
| Cathepsin proteases have distinct roles in trophoblast function and vascular remodelling M Screen, W Dean, JC Cross, M Hemberger Development 135 (19), 3311-3320, 2008 | 50 | 2008 |
| Altered expression and splicing of Ca2+ metabolism genes in myotonic dystrophies DM1 and DM2 A Vihola, M Sirito, LL Bachinski, O Raheem, M Screen, T Suominen, ... Neuropathology and applied neurobiology 39 (4), 390-405, 2013 | 34 | 2013 |
| Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagy M Screen, O Raheem, J Holmlund-Hampf, PH Jonson, S Huovinen, ... PLoS One 9 (3), e90819, 2014 | 23 | 2014 |
| Abnormal Splicing of NEDD4 in Myotonic Dystrophy Type 2: A Possible Link to Statin Adverse Reactions M Screen, PH Jonson, O Raheem, J Palmio, R Laaksonen, T Lehtimäki, ... The American Journal of Pathology, 2014 | 20 | 2014 |
Nicholas KatsanisGalatea BioVerified email at galatea.bio
